- Open Access
Improvement of the anticancer efficacy of PD-1/PD-L1 blockade via combination therapy and PD-L1 regulation
Journal of Hematology & Oncology volume 15, Article number: 24 (2022)
Immune checkpoint molecules are promising anticancer targets, among which therapeutic antibodies targeting the PD-1/PD-L1 pathway have been widely applied to cancer treatment in clinical practice and have great potential. However, this treatment is greatly limited by its low response rates in certain cancers, lack of known biomarkers, immune-related toxicity, innate and acquired drug resistance, etc. Overcoming these limitations would significantly expand the anticancer applications of PD-1/PD-L1 blockade and improve the response rate and survival time of cancer patients. In the present review, we first illustrate the biological mechanisms of the PD-1/PD-L1 immune checkpoints and their role in the healthy immune system as well as in the tumor microenvironment (TME). The PD-1/PD-L1 pathway inhibits the anticancer effect of T cells in the TME, which in turn regulates the expression levels of PD-1 and PD-L1 through multiple mechanisms. Several strategies have been proposed to solve the limitations of anti-PD-1/PD-L1 treatment, including combination therapy with other standard treatments, such as chemotherapy, radiotherapy, targeted therapy, anti-angiogenic therapy, other immunotherapies and even diet control. Downregulation of PD-L1 expression in the TME via pharmacological or gene regulation methods improves the efficacy of anti-PD-1/PD-L1 treatment. Surprisingly, recent preclinical studies have shown that upregulation of PD-L1 in the TME also improves the response and efficacy of immune checkpoint blockade. Immunotherapy is a promising anticancer strategy that provides novel insight into clinical applications. This review aims to guide the development of more effective and less toxic anti-PD-1/PD-L1 immunotherapies.
Immunotherapy, a promising anticancer strategy that improves the specificity and strength of the immune response to cancer, has been widely studied in recent years. Brakes on the immune system protect healthy tissues and organs from attack by the immune system; this brake system is hijacked by cancer cells to escape from the immune system or even turn against it . The programmed cell death 1 receptor (PD-1)/programmed cell death ligand 1 (PD-L1) pathway and the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) pathway constitute the well-known brake system of the immune system. Targeting these two pathways has been shown to be a successful anticancer strategy . Antibodies against the PD-1/PD-L1 pathway have been extensively applied to cases of melanoma, lung cancer, lymphoma, liver cancer, colorectal cancer, urothelial cancer, squamous cell carcinoma of the head and neck, cervical cancer, kidney cancer, stomach cancer and breast cancer . This monotherapy or combination therapy (as adjuvants or neo-adjuvants) produces a remarkable clinical response. A small number of cancer patients subsequently experience long-term remission. Nevertheless, the PD-1/PD-L1 blockade, similar to other anticancer treatments, is also limited by a low response rate in certain cancers, lack of known biomarkers, immune-related toxicity and innate and acquired drug resistance. To date, the clinical response to PD-1/PD-L1 blockade is barely 40% . Thus, identifying optimal biomarkers for screening cancer patients who are responsive to immune checkpoint blockades (ICBs) and accurately monitoring its therapeutic efficacy is of great clinical importance . In addition, it is important to precisely distinguish cancer cells from normal cells in ICBs, thus preventing severe adverse events such as discontinued treatment, dose reduction or even death due to immune-related toxicity . Similar to other anticancer treatments, some patients may not be sensitive to ICB or develop drug resistance after a period of medication. Elucidating the potential mechanisms of low responses and drug resistance to ICB will enhance their clinical benefits  and is key to improving the efficacy of immunotherapy .
In the present review, we first illustrate the biological mechanisms of PD-1/PD-L1 immune checkpoints and their role in both the normal immune system and TME, aiming to enhance current understanding of the immune checkpoint molecules PD-1/PD-L1. Combination therapy with other standard treatments, such as chemotherapy, radiotherapy, targeted therapy, anti-angiogenic therapy, other immunotherapies and even diet control, is expected to address the limitations of PD-1/PD-L1 blockade. Either upregulation or downregulation of PD-L1 expression in the TME improves the therapeutic efficacy of ICBs; a combination therapy of either with immunotherapy may represent a novel anticancer treatment and combinatorial drug design. This review summarizes the latest developments, prospects and challenges of the combination therapy of PD-1/PD-L1 blockade and PD-L1 regulation, aiming to provide novel ideas for developing more effective and less toxic anti-PD-1/PD-L1 immunotherapy.
Immune checkpoints in cancer therapy
The immune system in carcinogenesis
Advanced cancer has mainly been treated with radiotherapy and chemotherapy in recent decades. However, these treatments are unable to distinguish normal cells from cancer cells, leading to damage of normal cells, severe adverse events and even discontinuation of treatment. The normally functioning immune system is capable of accurately recognizing and eliminating cancer cells due to significant differences between normal cells and cancer cells, thus achieving precision killing. The interaction between cancer cells and the immune system used to be considered the main determinant factor for carcinogenesis .
However, recent evidence has shown that most new tumors formed in the esophagus would naturally be eliminated due to the weaker viabilities of these newly formed tumors that of adjacent mutant epithelial cells, rather than differences in survival due to the involvement of the immune system . Mutations are the potential origin of cancers. It was recently found that carcinogenicity is mediated by oncogenes (e.g., BRAFV600E), lineage-specific transcription factors (e.g., SOX10) and chromatin factors for regulating development (e.g., ATAD2) .
A recent study analyzed the relationship between immune response and tumor development , finding that chronic inflammatory cells secrete IL-6 and that transient inflammation leads to persistent reprogramming of epithelial cells leading to subsequent tumorigenesis, thus underscoring the role of the immune system in promoting tumorigenesis. Established anti-tumor immune responses suppress tumor development, but tumor cell clones that escape immune surveillance eventually develop into clinically visible tumors.
Cancer immunotherapy eliminates cancer cells by stimulating and enhancing immune function or regulating the immune state based on immune surveillance and immune editing. Of all immune cells, T cells are the most powerful tool for directly killing cancer cells and are characterized by high specificity, strong memory and high adaptability . The cancer-immunity cycle, in which cancer cells release specific antigens and the immune system is activated to kill them, is a cyclical process involving 7 steps: (1) Antigens are expressed and released by cancer cells; (2) cancer antigen processing and presentation; (3) T cell initiation and activation; (4) T cell migration to cancer lesions; (5) T cell penetration to cancer lesions; (6) recognition of cancer cells by T cells; and (7) elimination of cancer cells by T cells . Multiple factors in this cancer-immunity cycle are potential therapeutic targets for immunotherapies. Cancer cells have been reported to express high levels of immunosuppressive signal proteins, which contribute to avoid the attack of immune cells in the TME.
The basic biology of immune checkpoints
T cells are the most important part of the immune system, and their function is strictly and precisely regulated by the immune system, as multiple receptor molecules on the cell membrane transduce activating or inhibitory signals. Once T cells are activated by antigen stimulation, the immune system also initiates negative feedback to avoid continuous overactivation of T cells that causes excessive damage to the body. Inhibitory receptor molecules, known as checkpoint molecules, expressed on the surface of T cells are responsible for the negative feedback of the immune system, inhibiting the elimination of target cells by T cells by binding corresponding ligand molecules on the target cell surface. Checkpoint molecules are well studied in translational research in immunotherapies .
Immune checkpoint inhibitors (ICIs) have recently been highlighted for their functions in blocking the effect of inhibitory immune molecules on T cells and thus reducing immune tolerance to cancers; these ICIs have been widely analyzed by biopharmaceutical companies. Many immune checkpoints have been identified, including CTLA-4 and PD-1; while both have been thoroughly investigated, PD-1 has been of particular interest and has been widely applied in clinical practice.
The PD-1/PD-L1 pathway in cancer immunotherapy
PD-1 is a cell surface receptor that was initially found to be preferentially expressed in apoptotic cells . Later, PD-1 was identified as the key immune checkpoint for regulating T and B cell response thresholds to antigens. As a key checkpoint for T cells, PD-1 exerts a central role in regulating their cellular functions. The interaction between PD-L1 and PD-1 inhibits T cell function by inducing T cell exhaustion to promote immune evasion . Therefore, abnormally upregulated PD-L1 levels in cancer cells and some immune cells results in immune escape. Anti-PD-1/PD-L1 antibodies have become a hot topic in cancer immunotherapy.
PD-1, also known as CD279, is a type I transmembrane protein encoded by the PDCD1 gene of the CD28 immunoglobulin superfamily. It was first discovered and reported by Ishida et al. in 1992 [15, 16]. PD-1 is mainly expressed in activated CD4+ T cells, CD8+ T cells, natural killer T cells, B cells, macrophages, dendritic cells (DCs) and monocytes; its expression is induced by the T or B cell receptor pathway and enhanced by the stimulation of tumor necrosis factor . However, naive T and B cells barely express PD-1 [19,20,21]. PD-1 is comprised of 288 amino acids, including a single Ig variable-type (IgV) extracellular domain, a transmembrane domain and a cytoplasmic domain [22,23,24]. Its extracellular domain is similar to that of other members of the CD28 superfamily, containing an Ig variable-type domain that is important in ligand binding. N-terminal and C-terminal tyrosine residues in the cytoplasmic domain are involved in the formation of immunoreceptor tyrosine-based inhibitory motifs (ITIMs) and immunoreceptor tyrosine-based switch motifs (ITSMs), respectively [16, 24,25,26]; the latter is the main signal transduction domain of PD-1 and is closely related to the response activity of effector T cells.
The biological functions of PD-1 rely on two ligands: PD-L1 (also known as B7-H1 or CD274) and PD-L2 (also known as B7-H2 or CD273). The former was initially discovered by Dong et al. in 1999 , and the latter was discovered by Tseng et al. . PD-L1 is widely expressed in T cells, B cells, DCs, cancer cells, macrophages and others and is further upregulated by activated proinflammatory cytokines . It is mainly responsible for the immune escape of cancers.
The role of PD-1/PD-L1 in the immune system and in cancers
Under normal circumstances, the PD-1/PD-L1 pathway negatively regulates the immune system. ITSMs are a vital site for the biological functions of PD-1, which is phosphorylated by binding to PD-L1 and further induces immune inhibition by activating a series of intracellular pathways . Notably, the specific mechanisms by which PD-1 exerts its immunosuppressive effects differs between T and B lymphocytes .
Two signal pathways are involved in the immune response induced by T cells following pathogen invasion: the binding of major histocompatibility complexes (MHCs) on the antigen presenting cell (APC) surface to T cell receptors (TCRs) and the binding of APC-expressed immunostimulatory ligands to TCRs. As a result, activating or inhibitory signals are transduced to T cells and further regulate immune responses, such as T cell activation and exhaustion. PD-1/PD-L1 pathway can inhibit TCR-mediated T cell activation. In T cells, the engagement of PD-1 ligands and PD-1 results in the recruitment of SHP-1/2 (Src homology 2-containing tyrosine phosphatase 1/2) to the C-terminal of the ITSM. SHP-2 then dephosphorylates TCR-associated CD-3ζ and ZAP70, resulting in the inhibition of downstream signaling . Specifically, phosphatidylinositol 3-kinase (PI3K) pathway is suppressed, and the expression of the cell survival gene Bcl-XL is reduced . In addition, PD-1 inhibits TCR-induced activation of the PI3K/AKT pathway by activating PTEN . Moreover, by inhibiting the activation of the RAS-MEK-ERK pathway, PD-1 suppresses the proliferation of T cells . PD-1 has been reported to inhibit the activation of PKCδ, thereby decreasing the level of cytokine secreted by T cells, such as IFN-γ and IL-2 . Furthermore, PD-1 signaling regulates T cell metabolism by suppressing glycolysis and promoting lipolysis and fatty acid oxidation .
PD-1/PD-L1 interaction also inhibits the activation of B cells. When PD-L1 binds to PD-1, two tyrosines on its ITSM bind to the B cell receptor (BCR) and are phosphorylated, which recruits SHP-2 to the C-terminus of PD-1; SHP-2 is then phosphorylated. Subsequently, phosphorylated SHP-2 dephosphorylates the BCR, thus leading to acute Ca2+ disorder and long-term growth arrest. Therefore, PD-1 can impair the immune response of B cells to antigens .
The brake system of PD-1/PD-L1 was gradually developed during the course of evolution. In this brake system, negative feedback terminates the killing effect of the immune system in a timely manner and thus protects against excessive damage to normal tissues. Generally, the PD-1/PD-L1 pathway prevents the overstimulation of T cells and maintains immune tolerance to self-antigens, thereby reducing damage to surrounding tissues and preventing autoimmune diseases from developing [37, 38].
Cunningly, cancer cells escape the killing effect induced by T cells by utilizing this brake system. Overexpression of PD-L1 induces the development of an immunosuppressive TME in multiple cancers [39,40,41], including non-small-cell lung cancer (NSCLC) [42, 43], melanoma , renal cell carcinoma (RCC) , prostate cancer , breast cancer  and glioma .
Cancer cells highly express PD-L1 on the cell membrane. The binding of PD-L1 to PD-1 in T cells produces negative signals, inducing T cell apoptosis and reducing immunocompetence, which thus helps cancer cells escape immune surveillance and killing. In addition, the activation of the PD-1/PD-L1 pathway negatively affects the differentiation of effector T cells (Teff) and memory T cells (Tm) and upregulates the differentiation of regulatory T cells (Treg) and exhausted T cells (Tex), thereby significantly inhibiting the immune effect of T cells . The binding of PD-L1 to PD-1 also inhibits the proliferation of tumor-specific T cells and induces apoptosis by triggering the release of cytokines and cytotoxins . Cancer cells are also able to transport PD-L1 (carried in exosomes) to remote regions via the circulatory system. Therefore, they can remotely inhibit T cell activity before reaching metastatic lesions [51,52,53].
Blocking the binding of PD-L1 to PD-1 blocks this negative feedback and restores the function of T cells as well as their ability to kill cancer cells. Therefore, ICIs (PD-1/PD-L1 inhibitors) exert their anticancer effect via the immune system of the host, which is quite different from conventional cancer therapies. To date, the extraordinary efficacy of ICIs has been validated in multiple types of solid tumor cancers and hematological malignancies, with a sustained response and long-term survival benefits [54,55,56,57,58]. The inhibitory effect of PD-1/PD-L1 pathway on T cells is shown in Fig. 1.
The regulation of PD-1/PD-L1 in the TME
The TME is mainly composed of tumor-associated stromal cells, extracellular matrix (ECM) , nonmalignant cells surrounding malignant lesions and complex signaling networks for maintaining the internal interactions of the TME . TMEs not only promote the growth of cancer cells but also trigger invasion and metastasis . In addition, exosomes carrying noncoding RNAs are vital components of the TME and provide favorable conditions for the growth and migration of cancer cells .
The ECM is comprised of the basement membranes and interstitial matrix , an important barrier for metastasis. Various substances can be found in the ECM, including a large number of growth factors, cytokines and metalloproteinases secreted by cancer cells and other cells in the TME, as well as acidic substances produced by cancer metabolism. These acidic substances in turn maintain the weakly acidic TME, induce epithelial-to-mesenchymal transition (EMT) and promote the formation of a hypoxic microenvironment.
Regulatory effects of the TME on PD-1
The influence of PD-1 on immune suppression is very complicated. Previous studies have shown that PD-L1 expressed in cancer cells induces immune suppression through the apoptosis of activated T cells and the production of IL-10 by stimulated T cells . Furthermore, persistent activation of PD-1 decreases glucose metabolism in T cells and induces T cell incompetence and exhaustion [64,65,66]. In a chronic lymphocytic choriomeningitis virus (LCMV) infection mouse model, persistent antigen exposure exhausted T cells and completely or partially eliminated effector T cell function, which was reversed by the application of an anti-PD-L1 antibody . In addition to inducing cell differentiation into Tregs, PD-1 also regulates their development and cellular functions .
When stimulated by inflammatory factors, DCs upregulate PD-1 and thus significantly inhibit the antibacterial ability of the innate immune system . PD-L1 on the surface of macrophages regulates T cell migration, leading to the active immune expulsion of T cells from the TME . In addition to regulating immune tolerance, PD-L1 expressed in cancer cells quickly establishes a molecular barrier to fight against the killing effect of immune effector cells . By regulating the mTOR pathway, PD-1 expressed in melanoma cells promotes malignant growth .
As an immunosuppressive molecule, PD-1 inhibits the activation of T cells and induces their apoptosis. PD-1 is expressed at low levels in naive T lymphocytes and can be immediately activated by TCRs. Transforming growth factor β (TGF-β) is highly important in the process of PD-1 activation by TCRs . It induces abundant expression of PD-1 on the immune cell membrane following antigen stimulation, which may be attributed to a self-protection mechanism that prevents the overactivation of immune cells.
Other factors in the TME can also regulate the expression level of PD-1. IL-7, IL-15 and IL-21 can induce the activation of PD-1 in peripheral T lymphocytes . Although upregulated PD-1 does not affect the expansion and survival of T cells, it inhibits the secretion of cytokines . IL-12 and IL-6 induce PD-1 during the activation of TCRs by altering the chromatin structure of the PD-1 gene and activating the STAT3/STAT4 pathway, in which the proximal cis-acting elements in the promoter region of PD-1 and the transcription factors FOXO1 and NF-κB are needed . Moreover, the inflammatory factors TNF-α and IL-6 regulate the growth inhibition of T cells in osteoarthritis by blocking the interaction between PD-1 and PD-L1 via induction of the secretion of soluble PD-1 . In macrophages, interferon-α (IFN-α) regulates the expression of PD-1 by activating the JAK/STAT pathway. The interferon-sensitive responsive element (ISRE) in the promoter region of PD-1 enhances PD-1 transcription by forming the p48/STAT1/STAT2 complex with the JAK/STAT pathway . Additionally, IFN-α has been reported to synergistically regulate the expression of PD-1 with TCRs, producing a strong inhibitory feedback signal targeting the T cell-induced immune response .
Regulatory effects of the TME on PD-L1
PD-L1 causes T cell exhaustion and immune tolerance, which is the main factor for the immune escape of cancer cells [80, 81]. In addition to expression on the cell surface of T lymphocytes, B lymphocytes, DCs and macrophages, PD-L1 is also highly expressed on the surface of cancer cells. A variety of cytokines and exosomes in the TME inhibit the activation of cytotoxic lymphocytes (CTLs) by inducing the expression of PD-L1 and activating the PD-1/PD-L1 pathway, which eventually promote immune escape. The main regulatory factors for PD-L1 are reviewed below.
Interferon is a biologically active glycoprotein secreted following viral infections; it has antiviral, antibacterial, antitumor and immunomodulatory functions . Interferon-γ (IFN-γ) is a type II IFN that is mainly secreted by CD8+ T lymphocytes, NK cells and macrophages. IFN-γ can promote cancer growth and resist immune surveillance in certain circumstances . An increasing number of studies have validated the induction of cancer progression by IFN-γ through activation of PD-L1 and immune escape from the attack of certain subtypes of T cells [35, 84]. IFN-γ induces the expression of PD-L1 through multiple pathways, and analyzing these pathways facilitates the development of novel cancer therapies with fewer adverse events.
Tumor necrosis factor-α
As an inflammatory cytokine, tumor necrosis factor-α (TNF-α) activates inflammatory cells, kills pathogens, stimulates tissue repair and induces angiogenesis and connective tissue formation. However, it facilitates the immune escape of tumor cells by upregulating expression of PD-L1 . TNF-α is mainly produced by activated macrophages, T cells and NK cells, which bind to specific homotrimeric receptors on the cell membrane. By activating the NF-κB and ERK1/2 pathways, TNF-α upregulates PD-L1 expression at both the mRNA and protein levels . In addition, it stimulates cell growth, differentiation and apoptosis by inducing an inflammatory response through the activation of caspase, JNK and NF-κB. TNF-α also regulates the expression of PD-L1 by targeting miRNA-155 .
Interleukins (ILs) are a type of cytokine that are important in the maturation, activation, proliferation and immune regulation of immune cells and participate in multiple physiological and pathological processes. The proinflammatory cytokines IL-6 and IL-17 regulate the expression of PD-L1 in the TME. Epithelial growth factor receptor (EGFR) regulates the expression of PD-L1 as well as cell proliferation through the IL-6/JAK/STAT3 pathway [35, 73, 76,77,78,79,80, 82,83,84,85, 87]. In addition, overexpression of PD-L1 and knockdown of NKG2D enhance NSCLC patient tolerance of radiotherapy through the IL-6/MEK/ERK pathway . During carcinogenesis, IL-6 interacts with proteins involved in the formation of proliferative matrix and drives myeloid suppressor cells, thereby suppressing the immune system. Therefore, inhibiting the IL-6 pathway in the TME can enhance the cytotoxic response and sensitivity of cancer cells to NK cells by downregulating PD-L1 expression [89, 90].
Epithelial growth factor
Epithelial growth factor (EGF) is a small-molecule active peptide widely distributed in the human body. EGF contributes to cell growth by binding to corresponding receptors and activating the EGFR pathway. The EGFR pathway is well known for its regulation of cancer cell migration and proliferation. Moreover, EGFR mutations that trigger malignant proliferation and metastasis without the need to bind to EGF have been detected in many types of cancer cells. The EGFR pathway has also been reported to be involved in immune escape. EGF upregulates PD-L1 expression in lung cancer, breast cancer, head and neck cancer, esophageal cancer and salivary adenoid cystic carcinoma. MYC, an important transcription factor in cancers, is also involved in the regulation of PD-L1 by EGFR. In the EGFR-derived PD-L1 pathway, knockdown of MYC significantly downregulates PD-L1 expression [91,92,93]. MYC upregulates PD-L1 expression in T cell acute lymphoblastic leukemia (T-ALL) cells by directly binding to the promoter region of PD-L1, suggesting that the EGFR pathway is able to upregulate PD-L1 by upregulating MYC and promoting nuclear translocation . EGF not only induces the transcription of PD-L1 but also influences its protein stability and biological function. Additionally, the RAS-EGFR pathway is a classic oncogenic intracellular pathway that promotes tumor immunoreactivity by regulating the mRNA stability of PD-L1 . A previous study reported that K-RAS mutations in EGFR-driven lung cancer were associated with the expression of PD-L1 [96, 97].
Exosomes are extracellular vesicles (40–150 nm in diameter) released by almost all types of cells. They serve to transduce intracellular information to other cells and thus change their activity [98, 99]. Functionally, exosomes can regulate the growth, migration and angiogenesis of cancer cells [62, 100]. Cancer-derived exosomes can promote macrophage polarization into M2 macrophages and the expression of PD-L1 in these macrophages by upregulating phosphorylated STAT3 and further enhancing the immunosuppressive effect . Consistent with these findings, cancer-derived exosomes containing PD-L1 have been found to have a strong immunosuppressive effect . Cancer-derived exosomes in chronic lymphocytic leukemia induced an immunosuppressive response in monocytes. Monocyte activation is mainly induced by noncoding microRNAs contained in exosomes which activate the TLR7 pathway in monocytes, promoting monocyte-induced secretion of cytokines and eventually inducing the expression of PD-L1 . At present, research on exosomes is in its infancy, and we believe that the novel regulatory effects of exosomes on PD-L1 will be elucidated in the future.
The PD-L2 pathway in cancer immunotherapy
Molecular structure and distribution of PD-L2
PD-L2, also known as B7-DC, CD273 or PDCD1LG2, is the second most important ligand for binding to PD-1after PD-L1 . PD-L2 protein is a type I transmembrane protein encoded by the PDCD1LG2 gene, consisting of 270 amino acid residues and located on chromosome 9 with PD-L1 . The extracellular domain of PD-L2 consists of a membrane-distal immunoglobulin variable region and a membrane-proximal immunoglobulin constant region . Several studies have shown that the affinity of the PD-L2/PD-1 interaction is 3–4 times higher than that of the PD-L1/PD-1 interaction. This difference in affinity is attributed to the presence of a tryptophan residue unique to PD-L2 that binds to a binding site on the surface of PD-1 . PD-L2 is expressed primarily by dendritic cells, macrophages and cancer cells and downregulates the effector functions of T cells through the PD-1/PD-L2 axis in the TME . PD-L2 is expressed on activated CD4+ T cells and CD8+ T cell subsets, which can bind to PD-1 on T cells and inhibit T cell activation and proliferation .
PD-1/PD-L2 axis–mediated immune escape in cancer
The PD-1/PD-L2 pathway plays a major and complex role in the development and progression of cancer. The regulatory role of PD-L2 on T cells in the TME has been controversial. Some studies have shown that PD-L2 suppresses immune function by binding to PD-1 co-inhibitory receptors [103, 108]. However, other studies have shown that PD-L2 is a positive co-stimulatory molecule that stimulates T cell proliferation and cytokine production, exerting its functions through receptors other than PD-1 [28, 109]. In human T cells, PD-L2 acts only as a negative regulator of T cell activity, inhibiting T cell proliferation by interacting with PD-1, reducing cytokine production and leading to cell-cycle arrest [103, 107, 110]. Cancer cells frequently achieve immune escape through the PD-1/PD-L2 pathway mediated by potent inhibitory signals, thereby hindering the proliferation and function of effector T cells and forming an immune escape microenvironment that suppresses anti-tumor immunity [29, 111,112,113]. Tumors can induce immune escape via various mechanisms, thereby evading cytotoxicity from the immune system, and eventually progress and metastasize to other parts of the body [112, 113]. During tumorigenesis, the PD-1/PD-L2 signaling pathway can cause the exhaustion of T cell function and promote immune escape. The inhibitory effect of PD-L2 on T cell function involves the regulation of the PI3K/AKT and MEK/ERK pathways [110, 114]. T cell activity is regulated not only by receptor tyrosine kinases (RTKs) but also by non-RTKs. Studies on SHP-1 and SHP-2 have shown that they regulate T cell activity [115, 116]. PD-L2 inhibits the PI3K/AKT and MAPK pathways while also increasing the phosphatase activity of SHP-2 . PD-1/PD-L2-induced SHP-2 activation is involved in the early signaling pathways required for negative regulation of T cell function, such as cytokine production, and cell adhesion . Concomitant with T cell receptor (TCR) or B-cell receptor (BCR) cross-linking, PD-1 binds to PD-L2 and induces inhibitory signals by recruiting phosphatases (e.g., SHP-2) to the ITSM in the cytoplasmic tail of PD-1, resulting in the dephosphorylation of effector molecules involved in downstream TCR or BCR signaling.
Advances in PD-1/PD-L1 blockade-based combination treatment for cancer
As an adjuvant therapy, immunotherapy has become the next focus of competition in the clinical development of anticancer drugs. Immunotherapy has exhibited positive results both as adjuvant or neoadjuvant therapy in the clinical treatment of cancer. Since this review focuses on PD-1/PD-L1 blockade, immunotherapy and ICB mentioned later refer to PD-1/PD-L1 blockade, and ICI refers to PD-1/PD-L1 inhibitor.
Although great progress has been made in immunotherapy of cancer, they face challenges in cancer therapy mainly due to their low response rate. Atezolizumab is a human-derived anti-PD-L1 inhibitor approved by the Food and Drug Administration (FDA) in 2016 for the treatment of urothelial cancer. The clinical trial IMVigor 210 reported that the target response rate in patients with metastatic urothelial cancer expressing moderate to high levels of PD-L1 was only 27%. The PD-L1 inhibitor does not exhibit its predicted effects in up to 73% of patients with high levels of PD-L1, probably due to innate resistance [118, 119]. Unfortunately, this low level of therapeutic efficacy may reduce even further in patients responsive to ICB after a long-term treatment, a phenomenon known as acquired resistance. Most melanoma patients with a good response to ICB have been reported to only experience limited or transient benefits of ICB treatment [4, 9]. Although clinical evidence has supported the role of immune surveillance in controlling the recurrence and progression of some common types of cancers, such as prostate cancer, ovarian cancer, breast cancer and colorectal cancer with microsatellite instability-high (MSI-H) [13, 120], most patients have difficulty benefiting from ICB [9, 121,122,123]. To date, the molecular mechanisms underlying acquired resistance remain unclear, which significantly hinders the sustainability of ICB treatments. Hodgkin's lymphoma and melanoma have the best response to ICB, while head and neck squamous cell carcinoma and gastrointestinal cancers do not show high response rates. The response rate of NSCLC is medium, but the resistance rate remains high. In general, the following five mechanisms are thought to explain acquired resistance to ICB. First, tumor antigen presentation may be damaged due to the downregulation of MHC class I molecules or deficiency in antigen presentation induction; as a result, TCRs would be unable to recognize tumor antigens, and ICB would become invalid. Second, IFN-γ sensitivity may be lost. IFN-γ activates the JAK-STAT pathway, which upregulates MHC class I molecules and enhances anticancer immunity. However, inactivating mutations of JAK1 and JAK2 occur during ICI treatment, which would eliminate the sensitivity of cancer cells to IFN-γ. Third, neoantigens may be eliminated. Selective pressure in the TME during anti-PD-1 treatment may clear the neoantigen without the production of neoantigen-specific T cells, and therefore, immune escape could develop. Fourth, cancer-induced immune inhibition could occur. Stabilized β-catenin induced by WNT and the loss or mutation of PTEN facilitates the production of inhibitory cytokines, which would further prevent the infiltration of CD8+ T cells and inhibit their functions. Fifth, positive expression of other ICIs may occur. Several other immune checkpoints are produced during a single ICI treatment, thus resulting in acquired drug resistance [124,125,126,127].
Most conventional anticancer therapies also lead to drug resistance; however, combination with ICB may produce a satisfactory outcome by overcoming drug resistance. Combination therapy aiming to enhance anticancer efficacy is of major interest. ICB can be combined with chemotherapy, radiotherapy, surgery, targeted therapy and antiangiogenic therapy. Combination therapy with ICB not only enhances the capacity of antigen presentation and rescues exhausted effector T cells but also activates the immune system by releasing cancer antigens and stimulating them to kill cancer cells, which may yield enhanced anticancer efficacy . In addition, changes in killing factors and immune factors that attack tumor cells potentially influence immunotherapy efficacy.
Nevertheless, combination therapy is significantly restricted by the occurrence of severe adverse events (AEs). A recent systematic review and meta-analysis reported that the incidence of treatment-related AEs in combination therapy with chemotherapy and anti-PD-1/anti-PD-L1 antibodies was up to 97.7%, which is the highest of all types of combination therapies for cancers . This meta-analysis included 36 clinical trials with 43 regimens. Among them, the incidence of all-grade treatment-related AEs was 97.7%, and the most common AEs were anemia (45.4%) and hair loss (45.1%). The incidence of grade 3 and above AEs was 68.3%, and the most common AEs were neutropenia (19.6%) and anemia (11.4%) .
It also analyzed combination therapy with immunotherapy and targeted therapy in 45 clinical trials with 47 regimens. The incidence of all-grade treatment-related AEs was 94.5%, and the most common AEs were fatigue (34.3%) and diarrhea (31.7%). The incidence of grade 3 and above AEs was 68.3%, and the most common AEs were hypertension (9.3%) and hyponatremia (3.6%) .
Additionally, combination therapy with different immunotherapies was analyzed, including 54 clinical trials with 57 regimens. The incidence of all-grade treatment-related AEs was 86.8%, and the most common AEs were fatigue (26.4%) and diarrhea (21.1%). The incidence of grade 3 and above AEs was 35.9%, and the most common AEs were lipase increase (7.2%) and colitis (3.6%) .
Moreover, the meta-analysis analyzed combination therapy with immunotherapy and radiotherapy in 7 clinical trials with 7 regimens. The incidence of all-grade treatment-related AEs was 89.4%, and the most common AEs were dysphagia (30.3%) and nausea (24.9%). The incidence of grade 3 and above AEs was 12.4%, and the most common AEs were lymphocytopenia (10.3%) and dysphagia (8.8%) .
It is urgent to develop more reasonable combination therapies with fewer AEs and higher survival benefits. In the following section, we mainly summarize combination therapy with ICIs and others in NSCLC patients. ICB has achieved unprecedented efficacy in the treatment of NSCLC patients. However, only a small number of NSCLC patients have exhibited high response to ICB .
Some of these therapies are displayed visually in Fig. 2. PD-1 inhibitors nivolumab (Opdivo), pembrolizumab (Keytruda), cemiplimab (Libtayo) and PD-L1 inhibitors atezolizumab (Tecentriq), avelumab (Bavencio) and durvalumab (Imfinzi) are the PD-(L)1 inhibitors already approved. Numerous clinical trials have been designed to study the efficacy or safety of these approved PD-(L)1 inhibitors in combination with other approved standard treatment regimens. Key information on those clinical trials that have been completed is summarized in Table 1. As can be seen from the table, among those completed clinical trials, more than half of the combination regimens were based on the anti-PD-1 antibody pembrolizumab and nivolumab. The number of combination regimens of the two anti-PD-L1 antibodies atezolizumab and durvalumab also exceeded 30. There are few strategies regarding the combination therapy of cemiplimab and avelumab. From the combination regimen of nivolumab, it can be seen that nivolumab combined with CTLA-4 antibody ipilimumab with/without other treatment strategies has the largest number. Regarding the combination regimen of pembrolizumab, it can be seen that the number of regimens with combined targeted therapy (including anti-angiogenic therapy) is the largest. The number of regimens combined with chemotherapy was the second largest. Because these combination regimens are based on approved treatments, many of them are already approved for cancer treatment.
In addition to the above combination experiments, there are a large number of clinical trials studying the efficacy and side effects of approved/investigational PD-(L)1 inhibitors in combination with other cancer treatment regimens. Key information on representative ongoing clinical trials of such combination therapy is shown in Table 2. As can be seen from the table, most of the combination strategies are PD-1/PD-L1 blockade combined with chemotherapy, targeted therapy, radiotherapy and other immune checkpoint inhibitors. Chemotherapy, targeted therapy and radiotherapy are classic strategies for cancer treatment, and most approved cancer treatment strategies belong to them. Therefore, combination regimen containing these treatment strategies is likely to show numerous breakthroughs. PD-1/PD-L1 blockade has also been combined with many biotherapy regimens, such as cell therapy and vaccine. In addition, PD-1/PD-L1 blockade has also been combined with many novel cancer treatment options, such as electric field therapy, which has shown excellent efficacy in the treatment of glioma. More than half of the combination regimens belong to dual combination therapy, such as PD-1/PD-L1 blockade combined with chemotherapy. We can also see clinical trials with triple combination therapy. The results of these clinical trials will bring valuable data to improve the efficacy of PD-1/PD-L1 blockade.
Combination therapy with PD-1 and CTLA-4 blockers
Upregulation of other immune checkpoints is a potential cause of resistance to PD-1 inhibitors. Therefore, combination therapy with other ICIs can be a crucial strategy, including the combination of PD-1 inhibitors and CTLA-4 inhibitors, which is commonly used in clinical applications.
The combination of the anti-PD-1 antibody nivolumab and the anti-CTLA-4 antibody ipilimumab was used for the first time in humans in December 2009 and targeted two unrelated pathways . CTLA-4 produces a strong inhibitory signal to terminate the proliferation and activation of T cells, which can be blocked by CTLA-4 inhibitors, thus restoring the activation of T cells. Therefore, CTLA-4 mainly acts on interactive signal transmission between lymphocytes. PD-1 blocks the activation of the immune response . Flow cytometry also indicated that CTLA-4 and PD-1 inhibitors target proteins in different pathways . Additionally, a preclinical study demonstrated the synergistic effect of nivolumab and ipilimumab in a mouse cancer model .
Combination therapy was initially designed for populations that do not express PD-L1. The clinical trial CheckMate 227 (NCT02477826) reported that the efficacy of first-line combination therapy with nivolumab and ipilimumab was superior to that of platinum-doublet chemotherapy in advanced NSCLC patients with a high tumor mutation burden (TMB ≥ 10 mut/Mb); combination therapy with nivolumab and ipilimumab significantly enhanced the overall response rate (ORR, 45.3% vs. 26.9%) and median progression-free survival (mPFS, 7.2 months vs. 5.5 months) . The results of the CheckMate-227 trial on advanced NSCLC immunotherapy showed that treatment with nivolumab plus ipilimumab for 4 years provided robust and long-term OS benefits for patients with advanced NSCLC compared to that for chemotherapy regardless of PD-L1 expression or histological type. However, the incidence of immune-related AEs (irAEs) is significantly higher in combination therapy than in monotherapy and requires further analyzed .
The NEOSTAR phase II randomized clinical trial (NCT03158129) found that the combination of nivolumab plus ipilimumab resulted in a higher pCR rate (38% vs. 10%), less viable tumor (median 9% vs. 50%), and greater frequencies of effector, tissue-resident memory and effector memory T cells compared to nivolumab alone .
In the CheckMate 9LA trial, nivolumab + ipilimumab + two cycles of chemotherapy exhibited durable survival benefit compared with chemotherapy alone in advanced NSCLC patients with or without brain metastases . The POSEIDON trial reported for the first time that first-line durvalumab + tremelimumab + chemotherapy for metastatic NSCLC patients achieved both the PFS and OS endpoints, with an mPFS of 6.2 months and an mOS of 14 months, compared with 4.8 months and 11.7 months for chemotherapy alone .
Combination therapy with PD-1 and CTLA-4 blockers also showed benefit in other cancer types. In the CheckMate 648 trial, first-line use of nivolumab combined with ipilimumab in patients with advanced esophageal squamous cell carcinoma showed an OS benefit over chemotherapy alone. In patients with tumor cell PD-L1 expression of 1% or higher, the OS of nivolumab combined with ipilimumab was significantly longer than that of chemotherapy, with mPFS of 13.7 months and 9.1 months, respectively. Overall survival was also significantly longer with nivolumab plus ipilimumab than with chemotherapy in the overall population .The data from CheckMate 204 showed that combination nivolumab plus ipilimumab was efficacious in patients with asymptomatic melanoma brain metastases (MBM). The 36-month intracranial PFS was 54 1%, and OS was 71 9%, supporting first-line use of nivolumab plus ipilimumab. Some patients with symptomatic disease also achieve a long-term response with the combination . Dual PD-1 and CTLA-4 blockade by balstilimab and zalifrelimab combination showed promising and durable clinical activity in patients with recurrent and/or metastatic cervical cancer who relapsed after platinum-based therapy. Compared with the ORR of 4% to 14% for current second-line therapy, the combination therapy achieved an ORR of 25.6%, and the effect was durable, which is very promising. ORR was higher in PD-L1-positive patients and squamous cell carcinoma patients, reaching 32.8% and 32.6%, respectively . Other important clinical trials that assessed the efficacy of dual PD-1 and CTLA-4 blockade include NEOSTAR in NSCLC, CheckMate-214 in renal cell carcinoma, Checkmate-142 in colorectal cancer, CheckMate 067 in Melanoma, CheckMate 040 in hepatocellular carcinoma, CheckMate 743 in malignant pleural mesothelioma and CheckMate 648 in esophageal squamous cell carcinoma.
Combination therapy with chemotherapy
Chemotherapy was previously thought to directly or indirectly damage CTLs to inhibit the immune system. Recent studies have shown that chemotherapy not only directly kills cancer cells but also positively regulates the immune system to change the local tumor immune microenvironment. For example, chemotherapy induces immunogenic cell death (ICD) , promotes the release of tumor antigens and damage-associated molecular patterns (DAMPs) and activates DCs to increase cross-presentation of antigens. In addition, chemotherapy can also induce local production of CXCL10, recruit T cells to the tumor bed  and enhance the differentiation of antitumor-specific CTLs . Chemotherapy can also reduce the number of immunosuppressive cells, such as myeloid-derived suppressor cells (MDSCs)  and Tregs . In addition to prolonging the efficacy of immunotherapy, tumor shrinkage due to chemotherapy also reduces the risk of drug-resistant clones.
In the past decade, different types of chemotherapeutic drugs have demonstrated the ability to regulate multiple anticancer immune pathways . Given the wide application of chemotherapy in regulating the cancer immune response, combination therapy with ICIs and chemotherapeutic drugs remarkably improves clinical outcomes by enhancing the activity of CTLs. Systemic chemotherapy (SC) has been reported to have a negative immune effect, but local chemotherapy (LC) enhances the immune response. Combination therapy with LC and anti-PD-1 antibodies significantly promoted the immune response and survival rate of glioblastoma. The proliferation of antigen-specific effector T cell clones increases with the upregulated infiltration of cancer-associated DCs in LC-treated mice. In contrast, SC leads to systemic and intratumoral lymphatic exhaustion and reduced immune memory in long-term survivors .
Combination therapy with ICB and chemotherapy has been highlighted in the medical field and extensively evaluated in clinical trials, especially for treating advanced NSCLC. To date, combination therapy with ICB and standardized chemotherapy has achieved promising efficacy in NSCLC (KEYNOTE-189, IMpower130), small-cell lung cancer (SCLC, KEYNOTE-407, IMpower133) and triple-negative breast cancer (TNBC, KEYNOTE-355, IMpassion130).
The advantages of combination therapy with ICIs and chemotherapy have been confirmed . In the clinical trial KEYNOTE-021, the efficacy of combination therapy with pembrolizumab and chemotherapy was much higher than that of chemotherapy alone (55% vs. 29%), and it decreased the risk of disease progression by 47% .
Breast cancer is the most prevalent malignancy in females, and TNBC is the subtype with the highest recurrence and mortality rates. Hormone therapy and targeted therapy are ineffective for treating TNBC; it is mainly treated with conventional chemotherapy, but the efficacy is not ideal. Despite great advances in immunotherapy, its application to treatment of TNBC is a huge challenge. The combination of nab-paclitaxel and atezolizumab can effectively prolong PFS in patients with metastatic TNBC. However, the combination of paclitaxel and atezolizumab did not meet the primary endpoint of the clinical trial [149, 150]. This shows that the combination of different chemotherapy drugs with ICB may induce different therapeutic effects in the same type of tumor. A systematic analysis of the TME before and after chemotherapy and/or immunotherapy in TNBC patients would help to clarify the therapeutic mechanism and improve its efficacy. Paclitaxel-based chemotherapy may weaken the core anticancer immune cells. However, the activities of those cells can be significantly enhanced by ICIs, suggesting that combination therapy with paclitaxel and atezolizumab influences the efficacy of anti-PD-L1 antibodies in TNBC patients . The dosage form of chemotherapeutic drugs may also influence the efficacy of combination therapy. Paclitaxel nanomicelles can stimulate the antigen presentation of DCs and activate anticancer immunity. Combination therapy with low-dose paclitaxel nanomicelles and anti-PD-1 antibodies enhanced therapeutic efficacy by inducing CD8+ T cell-dependent anticancer immunity .
The combination of immunotherapy with chemotherapy also showed potential advantages in clinical trials compared to immunotherapy alone.
The CheckMate-816 phase III clinical trial showed that nivolumab plus adjuvant chemotherapy can markedly improve event-free survival in patients with resectable NSCLC, meeting its primary endpoint. Nivolumab plus chemotherapy exhibited a statistically significant clinical improvement in event-free survival compared to that of neoadjuvant chemotherapy alone.
In the KEYNOTE-407 (NCT02775435) randomized trial, pembrolizumab plus chemotherapy substantially improved OS and PFS in NSCLC patients compared to that of placebo plus chemotherapy .
Among the clinical trials on perioperative immunotherapies for NSCLC patients, IMpower010 is the first phase 3 clinical trial demonstrating that immunotherapy can considerably improve DFS in patients with early stage resectable NSCLC compared with best supportive care after adjuvant platinum-based chemotherapy. Based on this clinical trial, atezolizumab has been approved by the FDA as an adjuvant therapy for stage II-IIIA NSCLC patients whose tumors expressed PD-L1 ≥ 1% after surgery and platinum-based chemotherapy .
The NADIM trial showed that combination of neoadjuvant nivolumab with platinum-based chemotherapy is feasible in patients with resectable stage IIIA NSCLC. Neoadjuvant immunotherapy combined with chemotherapy has the potential to change some stage III NSCLC to curable disease .
Immunotherapy plus chemotherapy has demonstrated good therapeutic efficacy in unresectable locally advanced NSCLC. Five-year follow-up data from the PACIFIC study showed that the combination of durvalumab after chemoradiotherapy significantly improved OS and PFS in patients with unresectable stage III NSCLC. The KEYNOTE-799 trial showed that the combination of pembrolizumab plus chemoradiotherapy has promising anti-tumor activity in patients with unresectable, locally advanced, stage III NSCLC . The results of the GEMSTONE-301 trial showed that consolidation therapy with sugemalimab has superior efficacy and acceptable side effects in patients with stage III NSCLC after concurrent or sequential chemoradiotherapy.
The results of the KEYNOTE-811 trial showed that the addition of anti-PD-1 antibodies to the conventional treatment regimen (trastuzumab plus chemotherapy) for HER2-positive gastrointestinal malignancies improved therapeutic efficacy with a longer duration of survival . In addition, the adverse effects of this new treatment regimen (anti-PD-1 antibody + trastuzumab + chemotherapy) are also completely manageable. Based on these data, this new treatment regimen has been approved by the FDA as a first-line intervention for the treatment of HER2-positive gastric and gastroesophageal adenocarcinomas (GEACs).
However, due to the high heterogeneity of the TME, the overall efficacy of immunotherapy on tumors remains low, and the combination of immunotherapy and other therapies does not produce synergistic effects in all patients. A retrospective analysis of three cohorts of patients with advanced GEAC found that in patients with low PD-L1 expression in the tumor, compared with chemotherapy alone, the combination of chemotherapy and PD-L1 inhibitor had no significant effect on OS and PFS .The results of the GEMSTONE-302 trial on sugemalimab in the treatment of stage IV NSCLC showed that sugemalimab plus chemotherapy provided significant and clinically meaningful PFS improvement in different subtypes of metastatic NSCLC regardless of PD-L1 expression, with a 52% reduction in the risk of disease progression and death . Additionally, the combination therapy showed some benefit to OS, with a 2-year survival rate of 47.1%.
The CHOICE-01 trial showed that the combination of toripalimab with first-line standard chemotherapy resulted in longer PFS, higher objective response rate (ORR) and longer duration of relief in patients with advanced NSCLC with manageable side effects . In the IMpower132 trial, the addition of atezolizumab to the combination of pemetrexed + platinum complexes showed improved PFS in patients with stage IV nonsquamous NSCLC .
Combination therapy with radiotherapy
Radiotherapy is a local treatment that directly kills cancer cells with radiation. In addition, it triggers an antitumor immune response by releasing tumor-associated antigens, inducing type I interferons (IFNs) and changing the immunosuppressive TME. Immunotherapy aims to kill cancer cells and lesions by utilizing the immune system. Notably, the immunogenicity induced by radiotherapy in the body can stimulate the release of cellular contents, thus producing in situ vaccines, which is conducive to the anticancer effect. As a novel therapeutic strategy, combination treatment with radiotherapy and immunotherapy has achieved good clinical outcomes. To date, more than 100 clinical trials have been conducted to analyze the efficacy of combination treatment with radiotherapy (radioconjugates) and immunotherapy.
It has been reported that radiotherapy markedly upregulates the cell adhesion factors ICAM-1 and VCAM-1 on the surface of cancer cells. Combination treatment with radiotherapy and anti-PD-1 antibodies activates tumor-specific T cells in the TME . In addition, combination treatment with radiotherapy and anti-PD-L1 antibodies increases the infiltration of CD8+ T cells and reduces the accumulation of MDSCs and regulatory T cells, thereby improving anti-tumor immunity . Preclinical studies have shown that the addition of immunotherapy can achieve higher local control rates at the same radiation dose . A recent preclinical study demonstrated that radiotherapy facilitates immunotherapy in NSCLC by activating certain types of club cells. These cells subsequently release proteins that alleviate the inflammatory response and enhance the antitumor immune response by effectively inhibiting MDSCs, thereby significantly enhances the therapeutic efficacy of PD-1 inhibitors . The authors compared the efficacy of hypofractionated radiotherapy (different hypofractionated doses of radiotherapy) + PD-1 inhibitor and PD-1 inhibitor monotherapy in mouse NSCLC models and found that the tumor-free survival rate of mice in the combination group was 4 times that of the monotherapy group (40% vs. 10%). In addition, the secreted protein CC10 is thought to be a biomarker for the efficacy of combination treatment with radiotherapy and immunotherapy. Interestingly, the gene Scgb1a1, which encodes CC10, is a biomarker for radiotherapy-activated club cells.
Local radiotherapy (RT) induces an antitumor immune response partially by activation of immune evasion and tissue remodeling processes, e.g., via upregulation of PD-L1 and TGF-β expression. A combination treatment with Bintrafusp alfa (BA) and RT (BART) enhanced tumor infiltrating white blood cells, reprogramed the TME and reduced radiotherapy-induced fibrosis, leading to reconstitution of immune TME and spontaneous lung metastasis regression. Combination treatment with BART may further support clinical transformation by eradicating cancer lesions while preserving normal tissues .
Clear clinical evidence indicated that colon cancer patients with mismatch repair defects (MMRd) or those with microsatellite instability-high (MSI-H) respond well to immunotherapy, but the vast majority of microsatellite-stable (MSS) patients do not benefit from immunotherapy . PDAC is one of the cancers most resistant to immunotherapy. So far, immunotherapy alone has been proved to be ineffective for the treatment of PDAC patients, so it is necessary to carry out combination therapy based on the mechanism of intrinsic resistance to immunotherapy . A phase II trial study found that radiation therapy enhances the response to immunotherapy with ipilimumab and nivolumab in patients with MSS CRC and PDAC .
Recent studies have suggested that combination treatment with radiotherapy and anti-PD-1/anti-PD-L1 antibodies has better therapeutic efficacy compared with that of anti-PD-1/anti-PD-L1 antibodies monotherapy. Conventional fractionated radiotherapy, hypofractionated radiotherapy and stereotactic body radiation therapy (SBRT) have been applied in combination with radiotherapy and immunotherapy in advanced NSCLC patients, with radiotherapy administered prior to immunotherapy. The PEMBRO-RT clinical trial was the first to explore the efficacy of pembrolizumab as a maintenance therapy following SBRT in advanced lung cancer patients, which double that of the placebo group (41% vs. 19%) with an acceptable tolerance . A phase I clinical trial recruited patients with advanced solid tumors that had progressed after standard therapy and were given nivolumab + urelumab or nivolumab + cabiralizumab concurrently with and after SBRT. The results showed that 2 patients achieved complete response (5%), 7 patients exhibited partial response (17%), 12 patients showed stable disease (29%), 20 patients had disease progression (49%), mPFS and mOS were 3.0 months and 17.0 months, respectively. Patients with elevated serum IL8 prior to SBRT did not respond to treatment. These data demonstrate that SBRT in combination with nivolumab + urelumab or nivolumab + cabiralizumab is feasible in advanced solid tumors with modest antitumor activity and acceptable toxicity .
It remains unclear what is the optimal time for combination treatment with ICIs and radiotherapy to maximize the efficacy and minimizing the AEs in different types of cancers, which merits further investigation.
Combination therapy with surgery
Under normal circumstances, tissue damage caused by surgery can trigger an inflammatory response and the transformation to a Th2 immune response, involving enhanced activity of Tregs and expansion of MDSCs. Surgical stress results in dysfunction of NK and T cells. Therefore, the perioperative period is critical to enhance immunity and reduce cancer recurrence. Neoadjuvant therapy can preoperatively shrink cancer lesions, reduce surgical difficulty and resect micrometastases to decrease the risk of recurrence. This therapy may even be beneficial for patients who are unable to be surgically treated. A phase II clinical trial, CheckMate-159 (NCT02259621), showed the safety of preoperative neoadjuvant immunotherapy with nivolumab in NSCLC patients; this treatment was associated with fewer AEs, did not delay surgical treatment and caused a major pathological response in 45% of excised tumors. Intraoperative pathology also confirmed the massive infiltration of T cells and macrophages in cancer sections, suggesting that preoperative ICIs can enhance the antitumor immune response . The clinical trial NADIM (NCT03081689) on stage IIIa lung cancer patients showed that after preoperative neoadjuvant treatment with nivolumab + carboplatin + paclitaxel, the main pathological response (MPR), pathological complete remission (pCR) and partial remission (PR) in imaging examinations achieved 85.36%, 71.4% and 72%, respectively .
Taken together, these results indicate that neoadjuvant therapy with ICIs achieves extraordinary outcomes, although its efficacy needs to be validated in multicenter large-scale clinical trials. In addition, imaging-based response was significantly later than pathological response, which is a huge obstacle for the conventional preoperative imaging. At present, multiple clinical trials on neoadjuvant immunotherapies for NSCLC are ongoing, including NCT02938624, NCT03217071, NCT02818920 and NCT02259621, which are expected to provide more data.
Combination therapy with targeted drugs
Combination therapy with EGFR-TKI
EGFR mutations are the most common malignant drivers of lung cancer. NSCLC patients with EGFR mutations express PD-L1 at varying levels, and as a result, the therapeutic efficacy of combination treatment with EGFR inhibitors and ICIs remains controversial [174, 175]. EGFR mutations activate transcription factors such as STAT3, STAT1 and NF-κB, which further translocate into cell nuclei to induce PD-L1 expression. In addition to EGFR, PD-L1 can also be influenced by TP53, KRAS, STK11 and other genes. Tyrosine kinase inhibitors (TKIs) enhance immune presentation by upregulating MHC class I and II molecules . TKIs can enhance CTL-mediated anticancer activity, inhibit apoptosis of T cells and stimulate the production of IFN-γ . Moreover, TKIs reduce the infiltration of Tregs in the TME by accelerating Foxp3 degradation . Due to the immunomodulatory effects of TKIs, combination treatment with TKIs and immunotherapy is considered a promising strategy, although current findings are ambiguous.
However, several clinical trials have suggested that neither ICI monotherapy nor combination treatment with TKIs and ICIs is recommended for lung cancer driven by gene mutations due to the low efficacy, high incidence of AEs and rapid progression of diseases. The efficacy of PD-1 inhibitors in advanced NSCLC patients with EGFR/ALK mutations is generally lower than 5%, while that of targeted therapy is up to 70% . A retrospective study in Japan involving more than 20,000 advanced lung cancer patients with EGFR mutations found that the overall incidence of interstitial pneumonia or immune pneumonia was 4.8%: 4.6% in targeted monotherapy, 6.4% in ICI monotherapy and 25.7% in combination treatment with ICIs and TKIs . A number of clinical trials on TKIs were discontinued due to poor efficacy and severe AEs. A recent clinical trial analyzed immunotherapy efficacy and genetic data in 155 cancer patients. Of these patients, 2 lung adenocarcinoma patients with EGFR mutations developed drug resistance after chemotherapy and EGFR-TKI medication, and they further suffered rapid progression after switching to the PD-1 inhibitor nivolumab, with significant enlargement of cancer lesions by 53.6% and 125%, respectively . Representative clinical trials using PD-(L)1 inhibitor in EGFR-mutant NSCLC include KEYNOTE-010 and CheckMate 012 for PD-1 inhibitor monotherapy, and NCT02088112, TATTON, NCT01998126 for combination treatment with PD-(L)1 inhibitor and TKIs.
EGFR T790M mutation-negative and KRAS/TP53 comutation NSCLC patients were responsive to combination treatment with targeted therapy and ICIs, which may be attributed to the higher incidence of coexisting high expression levels of PD-L1 (≥ 10%), high percentage of CD8+ tumor infiltrating lymphocytes (TILs) (20% vs. 4%) and lower frequency of FOXP3+ TILs in EGFR T790M mutation-negative NSCLC patients compared to those in EGFR T790M mutation-positive patients . The relatively high TMB in NSCLC patients with KRAS mutations may be a potential explanation of their good response to ICIs, while that in patients carrying other key driver gene mutations (e.g., EGFR, ALK, ROS1) was relatively low .
Thus, targeted therapy is still preferred for EGFR-mutant lung cancer patients. The efficacy and safety of combination treatment with ICIs and TKIs in lung cancer patients carrying driver gene mutations remain uncertain and should be further analyzed to identify specific populations that may benefit from it.
Combination therapy with agonists of the STING pathway
MYC binds to the DNMT1 promoter and activates its transcription, thereby inhibiting the cGAS-STING pathway through epigenetic regulation . The cGAS-STING pathway is vital in linking innate immunity and adaptive immunity against cancers . Cancer cells can escape immune surveillance by inhibiting the cGAS-STING pathway . The cytosolic DNA-sensing cGAS-STING pathway has therefore been widely analyzed in immune activation [184, 185].
The surface expression of PD-L1 can be upregulated by targeting the DNA damage response (DDR) protein poly ADP-ribose polymerase (PARP) and checkpoint kinase 1 (CHK1) . PARP is a DNA repair enzyme, and its inhibitors (PARPis) significantly upregulate PD-L1 , which activates the STING/TBK1/IRF3 pathway, upregulates chemokines such as CXCL10 and CCL5  and induces the activation of CTLs . DDR protein inhibitors also upregulate chemokines such as CXCL10 and CCL5 by activating the STING/TBK1/IRF3 pathway, thereby inducing the activation of CTLs .
By promoting the accumulation of cytosolic DNA fragments, PARPis induce antitumor immunity independent of BRCAness by activating the DNA-sensing cGAS-STING pathway and stimulating the production of type I interferons. ICB further enhances the regulatory effects of PARPis . Therefore, PARPis are promising immunomodulators for ICB in cancer treatment.
Remarkable results have been achieved in the maintenance treatment of recurrent ovarian cancer and breast cancer with PARPis combined with ICIs [190,191,192]. At present, four PARPis have been approved by the FDA, including olaparib, rucaparib, talazoparib and niraparib. SCLC, which is highly sensitive to platinum-based chemotherapy, usually express high levels of PARP1, suggesting the important role of DNA damage repair . A phase II randomized clinical trial showed that combination treatment with the PARPi veliparib and standard chemotherapy achieved an ORR of 39% in SCLC patients . Other representative clinical trials combining PARPi and PD-(L)1 inhibitors include TOPACIO/Keynote-162, NCT04681469, NCT04837209, NCT03824704, NCT02873962, NCT03694262, NCT03737643, NCT03642132 and NCT03598270. Currently, the application of PARPis combined with ICIs in the treatment of SCLC is in its infancy, and the specific mechanisms need further investigation. In addition, combination treatment with ICB and inhibitors of DDR, ATR, ATM, CHK1 and MK2 requires in-depth examination.
Combination with other targeted therapy
ICB with anti-G-CSF antibodies and Src inhibitors is capable of blocking neutrophil infiltration, thereby preventing pY696-EZH2-driven brain metastases. EZH2 is upregulated in brain metastases and phosphorylated at tyrosine 696 by Src tyrosine kinase, which changes its binding preference from histone H3 to RNA polymerase II and switches EZH2’s function from a methyltransferase to a transcription factor responsible for upregulating c-JUN. Upregulation of c-JUN further triggers the activation of carcinogenic inflammatory cytokines such as granulocyte-colony stimulating factor (G-CSF), which accelerates brain metastases by recruiting Arg1-positive and PD-L1-positive immunosuppressive neutrophils into the brain . The therapeutic efficacy of combination treatment with anti-G-CSF antibodies or ICB for treating brain metastases has been verified in multiple mouse models.
PGE2 driven by cyclooxygenases is produced by various types of cancers and consequently induces malignant growth by escaping type I interferon and/or T cell-induced eradication of cancer cells. The synergistic effect of cyclooxygenase inhibitors combined with ICB has been proven to significantly induce cancer cell eradication .
Combination treatment with ICB and MDSC-targeted therapy in primary and metastatic castration-resistant prostate cancer (CRPC) presents a strong synergistic response by upregulating interleukin-1 (IL-1) receptor antagonists and inhibiting proinflammatory cytokines released by prostate cancer cells .
Reasonable sequencing assists in overcoming innate and acquired drug resistance following combination treatment with PD-1/PD-L1 inhibitors and MAPK-targeted therapy. Clinical benefits obtained from MAPK inhibitors (MAPKis) are linked with prior ICI treatment. Anti-PD-1/PD-L1 antibody lead-in before MAPKi treatment not only inhibits melanoma brain metastasis (MBM) but also enhances the survival rate of mice through the potent clonal expansion of T cells in intracranial and extracranial metastasis sites .
The KEYNOTE-775 phase III clinical trial showed that patients with advanced endometrial cancer treated with the anti-PD-1 monoclonal antibody Pembrolizumab plus the oral multi-receptor TKI Lenvatinib exhibited significant improvements in OS and PFS compared to that seen with chemotherapy alone. The median PFS (7.2 months vs. 3.8 months) and median OS (18.3 months vs. 11.4 months) of the Pembrolizumab/Lenvatinib group were significantly higher than that for the chemotherapy group.
Studies have shown that intermittent PI3K inhibition can attenuate the inherent immunosuppressive activity of Pten-null cancer cells and transform cold tumors into a state of high T cell infiltration, paving the way for successful immune checkpoint therapy .
Pattern recognition receptors (PRRs) are molecules central to initiating and maintaining innate immunity and which include TLRs, the RGR family and cGAS-STING; they monitor local infection and/or tissue damage, thereby preventing systemic infection the production of malignant cells. TLRs are the best-studied PRRs and central to the activation of the innate immune response. TLRs agonists are a major direction for anti-tumor immunotherapy. In addition, as TLRs agonists activate innate immunity and are the cornerstone of activation of the adaptive immune response, they have an inherent advantage when combined with anti-PD-(L)1 therapy.
Intratumoral immunotherapy using TLR agonists aims to induce or enhance local tumor inflammation and immunity by mimicking intracellular microorganisms (viruses or bacteria), thereby evoking cytotoxic CD8 + T cell responses, promoting the infiltration of TILs, and stimulating CD4 + T cells to produce effector molecules such as IFN-γ, which in turn enhances the anticancer effects of anti-PD-1 antibodies. In addition, the use of TLR agonists as vaccine adjuvants is also a direction of future development. However, as the systemic administration of TLR agonists may lead to systemic inflammation and treatment-related side effects, current clinical development has focused on local intratumoral injection to localize inflammation to the tumor [200, 201].
Combination therapy with anti-angiogenic drugs
Local hypoxia and low pH levels caused by the abnormal structure and function of tumor blood vessels result in an inhibitory tumor immune microenvironment. Hypoxia triggers the accumulation of MDSCs and accelerates the differentiation of tumor-associated macrophages (TAMs) into immunosuppressive M2 macrophages . In addition, hypoxia indirectly stimulates the aggravation of Tregs by upregulating CC chemokine ligands. It also upregulates PD-L1 expression in cancer cells and TIM-3 and CTLA4 expression in TAMs, MDSCs and Tregs and indirectly upregulates PD-1 expression in CD8+ T cells, thus inhibiting the activation of immune cells. The increased tumor vascular permeability and decreased lymphatic vessels contribute to the high tumor interstitial fluid pressure (TIFP), which hinders immune effector cells from entering the cancer lesion .
Anti-angiogenic drugs reprogram the TME by normalizing immature blood vessels and reducing the activities of immunosuppressive cells such as MDSCs and Tregs . T cells that bind to tumor antigens are more effectively activated through blocking VEGF-induced inhibition of DC maturation. The normalized tumor vascular structure is favorable to the infiltration of CTLs into cancer lesions. However, high-dose antiangiogenic drugs result in excessive vascular pruning, which further exacerbates the hypoxia and acidosis of the TME. In addition, high-dose anti-VGEF drugs can also accelerate the deposition of ECM, local hypoxia and immunosuppression . However, low-dose vascular endothelial growth factor inhibitors can reduce the sprouting of immature blood vessels and make them structurally and functionally normal, facilitating the delivery of chemotherapy drugs and promoting the infiltration of killer T cells into tumors .
Anti-angiogenesis therapy promotes the intratumoral infiltration of PD-1+ Tregs. There are two types of TAMs. They are derived from monocytes or alveolar cells. The former type relies on CSF-1R, and the latter is sensitive to cisplatin and contributes to the establishment of a TGF-β-rich TME. Dual inhibition of TAMs with CSF1R inhibitors and cisplatin suppresses Tregs, which redirect anti-PD-1 antibodies to CD8+ T cells. As a result, immunotherapy with antiangiogenic drugs exerts an excellent efficacy to eradicate cancer lesions in most cases .
Anti-angiogenic therapy can enhance the efficacy of immunotherapy by downregulating immunosuppressive factors during tumor angiogenesis and reversing the de-energized state of endothelial cells . As a malignant ecosystem, the TME is composed of “normal cells” that behave extremely abnormally in addition to cancer cells. Endothelial cells in tumor vasculature are a good example. Despite its abundant vasculature, the tumor is still highly hypoxic due to the abnormal function and structure of these blood vessels. Some multi-target TKIs can simultaneously inhibit fibroblast growth factor receptors (FGFR) and platelet-derived growth factor receptors (PDGFR), thereby reducing the activity of cancer-associated fibroblasts . How to combine targeted therapy that brings “normalized microenvironment” with immunotherapy to exert excellent efficacies in cancer patients still needs to be explored.
The clinical trial IMpower150 assessed the efficacy and safety of combination treatment with atezolizumab and bevacizumab/chemotherapy on newly treated stage IV nonsquamous NSCLC. Compared with bevacizumab + carboplatin + paclitaxel, the addition of atezolizumab to the above regimen presents controllable side effects and satisfactory anticancer activity, which provides a novel option for treating nonsquamous NSCLC patients . The phase 1a/b JVDF clinical trial explored the efficacy of ramucirumab combined with pembrolizumab on advanced NSCLC and found it achieved an ORR of 30% with controllable side effects . Taken together, these studies suggest that combination treatment with ICIs and antiangiogenic drugs is a promising strategy, and its efficacy, safety and mechanisms should be further analyzed.
The influence of dietary composition on immunotherapy
The effect of diet composition on immunotherapy has shown broad importance in cancer treatment.
Vitamin C is an electron donor involved in the biochemical reactions of cancer stem cells and the synthesis of collagens and hypoxia-inducible factors, which are important for metastasis as they regulate ECM reprogramming . Specific doses of vitamin C are able to prevent glycolysis in cancer cells as well as the synthesis of nitroso groups, indicating the importance of this vitamin for cancer treatment . Recent studies have shown that vitamin C indirectly enhances the anticancer immune response of anti-PD-L1 antibodies . High-dose vitamin C regulates the infiltration of immune cells in the TME and delays malignant growth in a T cell-dependent manner. Vitamin C not only enhances the cytotoxic activity of adoptively transferred CD8+ T cells but also has promoted the therapeutic efficacy of immune checkpoint therapy (ICT) . The synergistic effect of vitamin C and anti-PD-1 antibodies has been validated in mouse models of lymphoma [211, 213]; it enhances the intratumoral infiltration of CD8+ T lymphocytes, macrophages, DCs and NK cells and upregulates the expression of granzyme B and IL-12 .
Stimulator of interferon genes (STING) agonists derived from the microbiota regulate macrophage polarization and NK cell-DC crosstalk by inducing the production of type I interferon (IFN-I) in intratumoral monocytes. Microbiota modulation with a high-fiber diet enhances anticancer the efficacy of ICB by triggering the IFN-I/NK cell/DC cell axis .
Ketogenic diet is becoming popular. A recent study reported that energy change induced by a ketogenic diet enhanced the efficacy of anti-CTLA-4 immunotherapy by downregulating PD-L1 expression and upregulating expression of IFN-I and antigen presentation genes. The activated AMPK pathway is responsible for phosphorylating PD-L1 at Ser283, which in turn disrupt its interaction with CMTM4 and degrades PD-L1. Moreover, activated AMPK also represses PRC2 by phosphorylating EZH2 and eventually upregulates the expression of IFN-I and antigen presentation genes .
The recently proposed fasting/fasting-mimicking diet reduces the survival of cancer stem cells and delays the progression of TNBC by inhibiting the activity of glucose-dependent protein kinase A. In differentiated tumor cells, the activation of starvation escape signaling pathways can be blocked using certain inhibitors to inhibit tumor progression and improve patient outcomes .
Alcohol consumption induces ALDH2 and subsequently upregulates PD-L1 expression in CRC, thereby protecting it from immune surveillance. Therefore, the combination of ALDH2 inhibition and anti-PD-1 therapy enhances the anti-tumor immunity and can be used as a novel strategy to enhance the efficacy of ICB in CRC patients, especially those who consume alcohol .
Combination therapy with TIL adoptive cell therapy
Although great progress have been made in utilizing ICB for treating NSCLC, a considerable number of NSCLC patients do not benefit from the treatment. Additionally, its efficacy in combination treatment is far from satisfactory. A relevant study reported that most NSCLC cases relapsed within 12 months of combination treatment with ICB and platinum-based chemotherapy . Notably, some NSCLCs are cold tumors that lack activated tumor-specific T cells, which is a vital reason of primary resistance to ICB. More effective combination treatment regimens are needed to turn the cold advanced NSCLC into hot tumors. Some studies proposed that adoptive cell therapy (ACT) using the patient's own T cells may be ideal for regulating the TME.
A previous study demonstrated that some melanoma patients benefitted from ACT using TILs extracted from tumor tissue from patients ; this therapeutic strategy has also been reported to be effective in treating cholangiocarcinoma , cervical cancer , colorectal cancer  and breast cancer . A recent phase 1 clinical trial (NCT03215810) was the first study to analyze the efficacy of TILs combined with nivolumab in advanced NSCLC patients and found that 2 patients achieved sustained complete remission 1.5 years later .
Combination with cell therapy
The combination of PD-1 blockade and third-generation anti-GD2-CAR-T cell therapy produced robust responses in melanoma patients . A preclinical study showed that CAR-T cell therapy targeting PD-1-blocking scFv improves the viabilities of tumor-specific T cells. The scFv secreted by CAR-T cells are localized in the tumor, which may prevent the cytotoxicity associated with systemic checkpoint inhibition .
Combination with oncolytic virus therapy
Oncolytic virus therapy can increase the activities tumor-specific effector and memory T cells that attack tumor cells [226, 227]. Therefore, oncolytic virus therapy is also considered a type of immunotherapy. Engineered oncolytic viruses recombinantly expressing monoclonal antibodies against the immunosuppressive molecule TIGIT have been constructed in a previous study. These recombinant oncolytic viruses could turn the “cold” TME to “hot” and induce an effective anti-tumor immune response . In addition, combination of these viruses with PD-1 inhibitors or LAG-3 inhibitors resulted in better efficacy and caused tumor regression.
A novel combination of the colony-stimulating factor 1 receptor (CSF-1R) inhibitor PLX3397, oncolytic viruses and anti-PD-1 antibodies has been analyzed and significantly controls malignant growth and prolongs the survival of colorectal cancer (CRC) mouse models. Approximately 43% and 82% of CRC mice implanted with CT26 and MC38 cells survived long-term after the triple combination treatment, respectively, which can be attributed to reprogrammed antitumor immunity by enhancing T cell infiltration and CD8+ T cell function .
Combination with mechanical immune checkpoint blockade
In addition to traditional immune checkpoints, one study have proposed the concept of mechanical immune checkpoints, which can be used for developing a new generation of targeted therapies, thereby improving the efficacy of cancer immunotherapy . The study found that cancer-cell stiffening could serve as a mechanical immune checkpoint. By depleting the cholesterol level in the plasma membrane of tumor cells to increase the stiffness of cancer cells, the cytotoxicity against stiffened cancer cells can be augmented, and the effect of adoptive T cell therapy can be improved.
Combination with immunomodulatory vaccines
A phase I/II clinical study showed that the combination of nivolumab and IO102/IO103, an investigational vaccine targeting indoleamine 2, 3-dioxygenase (IDO) and PD-L1, showed an ORR of up to 80% in metastatic melanoma patients . This combination of immunomodulatory vaccine with PD-1 inhibitor significantly reduced tumor burden and increased the PFS to 26 months.
The effects of circadian rhythm on the efficacy of immunotherapy
A recent study found for the first time an evident correlation between the body's biological clock and circadian rhythm and the efficacy of immune checkpoint inhibitors. If at least 20% of the dose was infused after 16:30 pm during treatment, the patient's risk of death was doubled, and the 5-year survival rate was also reduced by 20% . Some small-scale clinical studies showed that the immune response activated by the injection of a vaccine between 09:00 and 11:00 a.m. was significantly better than that injected between 15:00 and 17:00 p.m. . Cytokine immunotherapy with recombinant human IL-2 injections also seems to exhibit differences in efficacy at different times of day .
Combination with DNA damage response (DDR)-targeted therapy
Immunotherapy has revolutionized cancer treatment and dramatically improved the outcomes in patients with multiple tumor types. However, most patients still do not benefit from these treatments, especially those lacking pre-existing T cell infiltration. Loss of DDR is a major determinant of tumor immunogenicity. Growing evidence supports the following roles of DDR-targeted therapy in tumor immunity : (1) promoting antigenicity by increasing mutability and genomic instability, (2) enhancing adjuvanticity by activating cytosolic immunity and immunogenic cell death and (3) favoring reactogenicity by modulating of factors that control the tumor-immune cell synapse.
Combination with inhibition of M2 macrophages
Histamine from allergic reactions can activate macrophages and inhibit the anti-tumor immune response of T cells, thereby causing resistant to PD-1 inhibitors. HRH1-activated macrophages polarize to an M2-like immunosuppressive phenotype and increased expression of the immune checkpoint VISTA, leading to T cell dysfunction . H1-antihistamines can effectively reverse the immunosuppressive effects of M2 macrophages, thereby restoring T cell activity and the therapeutic efficacy of anti-PD-1/CTLA-4 treatment. Targeting HRH1 and VISTA may identify powerful combination therapies to overcome ICB resistance.
Improvement of ICI efficacy by regulating the expression of PD-L1
In addition to combination treatment with ICIs, other interventions that influence the expression of PD-L1 also affected the efficacies of PD-(L)1 blockade. PD-L1 is upregulated on the surface of many types of cancer cells by IFN-γ and TNF-α, and the regulation involves some endogenous carcinogenic pathways (e.g., the PI3K-AKT and AMPK pathways). Upregulated PD-L1 assists cancer cells in immune escape by negatively regulating antitumor immunity after binding to PD-1 . Altered PD-L1 expression (either through upregulation or downregulation) yields better efficacy in combination with immunotherapy. After downregulation of PD-L1 expression, the inhibited PD-L1/PD-1 axis releases the brake on the immune system. In contrast, upregulated PD-L1 turns cold tumors into hot tumors; therefore, the PD-L1/PD-1 axis might have more power to inhibit the anti-tumor immune system. Targeting this pathway can also produce good therapeutic effects.
Targeting PD-L1 regulation can also produce good therapeutic effects. A multistage sensitive nanocomplex (MUSE) loaded with PD-L1/CD47 multiple targeting CRISPR/Cas9 system was developed for coactivation of both T cells and macrophages-mediated antitumor immune response . The prepared MUSE has some beneficial characteristics, including prolonged blood circulation, rapid response to the MMP-9-rich TME, enhanced lysosomal escape, rapid nuclear localization and high transfection efficiency. With these advantages, MUSE loaded with MT-CRISPR/Cas9 demonstrated effective elimination of PD-L1 and CD47 in tumor cells and activated both innate and adaptive antitumor immunity, thereby significantly improving overall survival in mouse model of melanoma with no detectable off-target effects. This study provides new avenues for the development of anticancer treatment regimens and paves the way for CRISPR-based anticancer therapies in the future.
Signaling pathways for regulating the expression level of PD-L1
Several factors have been found to abnormally enhance PD-L1 expression, including genomic alterations, constitutive activation of oncogenic pathways (e.g., activation of EGFR, mTOR, PI3K, AKT and AMPK pathways and deficiency of PTEN) [175,176,177,178,179] and exogenous factors (e.g., IFN-γ, TGFβ1, TNF-α and IL-17) [85, 179,180,181].
Factors that regulate the expression level of PD-L1
Many factors affect the expression levels of PD-L1 in the TME and circulation and thus can affect the efficacy of ICB. Here, we categorize these factors as endogenous factors, signaling pathway changes and external factors. Table 3 summarizes representative preclinical studies of influencing factors. From these studies, we can see that the expression of PD-L1 is complexly regulated. In addition, most studies provide strategies to exploit the expression changes of PD-L1 to enhance the therapeutic effect of ICB.
Endogenous factors refer to changes in oncogenes or tumor suppressor genes that enhance the expression of PD⁃L1 in cancer cells, such as overexpression of MYC, mutation of the RAS oncogene and activation mutation of the EGFR, which can upregulate PD-L1 expression and thus promote immune escape.
The transcription factor Myc is usually overexpressed in human cancers and regulates many genes associated with cell proliferation and survival . Casey et al.  found that Myc directly activated the transcription of CD47 (also known as IAP) and PD-L1, which are involved in innate and adaptive immune escape. CD47 is an antiphagocytic protein that is overexpressed in multiple types of cancers and transmits a “do not eat me” signal to macrophages and DCs [188, 190]. The expression levels of CD47 and PD-L1 are related to anti-angiogenesis and the induction of senescence in T cell acute lymphoblastic leukemia (T-ALL) cells .
The RAS-EGFR pathway is a classic intracellular signaling pathway, and carcinogenic RAS signaling has been shown to regulate the mRNA stability of PD-L1 to promote tumor immune reactivity . In TNBC, EGF-induced interaction between PD-L1 and PD-1 requires the expression of β-1,3-N-acetylglucosaminyl transferase (B3GNT3). Downregulation of B3GNT3 can enhance the antitumor immune effect of cytotoxic T cells. Monoclonal antibodies against glycosylated PD-L1 (gPD-L1) blocked the PD-L1/PD-1 interaction and promoted the internalization and degradation of PD-L1 .
Caspase 8 is a caspase involved in cell apoptosis and other cellular behaviors. Its mutation is linked with increased cancer risk, and low expression of Caspase 8 is closely correlated with poor prognosis. Caspase 8 induces the degradation of PD-L1 by upregulating TNFAIP3 (A20) expression, which is an ubiquitin editing enzyme that results in PD-L1 ubiquitination. Caspase 8 is a promising biomarker for predicting the sensitivity to anti-PD-L1/PD-1 immunotherapy .
Multispecific platinum (IV) complex DNP exhibits high cytotoxicities and anti-inflammatory properties that are superior to those of NP (another multispecific platinum [IV] complex), cisplatin and naproxen. Cyclooxygenase-2(COX-2) plays an important role in the progression of breast cancer, correlating with the levels of PD-L1. Mechanistic studies revealed that DNP reduces the expression of COX-2 and PD-L1 in vitro and in vivo, suppresses the secretion of prostaglandin, reduces the expression of BRD4 and phosphorylated Erk1/2 and blocks the oncogene c-Myc in breast cancer cells .
The targets of sunitinib and inhibitory immune checkpoints and suppressive immune cells were significantly positively correlated. Sunitinib modulates the expression of tumor PD-L1 via p62, which binds to PD-L1 and specifically enhance its translocation into autophagic lysosomes for degradation. Sunitinib showed synergistic anticancer efficacy with CTLA-4 blockade in immunocompetent mice models of melanoma and NSCLC by increasing tumor-infiltrating T cell activity. In anti-PD-1-treated NSCLC patients, higher PD-L1 levels and lower p62 levels was observed in the tumor of responders compared to those of nonresponders .
Signaling pathway changes
Multiple oncogenic pathways are involved in the posttranscriptional regulation of PD-L1FGFR2 is highly expressed in CRC and upregulated PD-L1 expression in CRC xenograft in the mice through the JAK/STAT pathway . Loss of function or mutations of the JAK/STAT pathway induce loss of PD-L1 expression in cancer cells, leading to primary and acquired resistance to anti-PD-1 antibodies. In addition, the inactivated IFNGR/JAK/STAT pathway is detected in recurrent patients following ICB . The PTEN/PI3K/AKT/mTOR pathway is responsible for the transcription of PD-L1. PTEN deficiency or mutations of PIK3CA upregulate PD-L1 expression by activating the AKT/mTOR pathway in glioma, breast cancer and prostate cancer . Interestingly, upregulated PD-L1 expression in a mouse model of lung squamous cell carcinoma accelerated PTEN deficiency . Thus, PTEN has been suggested to interact with PD-L1 in cancer.
Ketogenic diet activates AMPK pathway through inducing energy changes, which enhances the immunotherapy efficacy by downregulating PD-L1 expression and upregulating expression of IFN and antigen presentation genes . Metformin is able to activate AMPK, which directly phosphorylates S195 on PD-L1. S195 phosphorylation impairs glycosylation of PD-L1, leading to its accumulation in the endoplasmic reticulum and the degradation of endoplasmic reticulum-associated proteins (ERAD). In breast cancer patients treated with metformin, activated AMPK and downregulated PD-L1 expression were observed in the tumor tissue . Blocking the inhibitory signal of PD-L1 by metformin can enhance the activity of CTLs against cancer cells. Therefore, ketogenic diet or AMPK agonists are recommended for combination treatment with immunotherapy in cancer patients.
Curcumin inhibits the growth and reduces surface PD-L1 expression in Hep3B cells. Curcumin has a synergistic effect with anti-PD-1 antibodies in slowing Hep3B cell proliferation, activating lymphocytes, inhibiting immune evasion and downregulating TGF-β1 expression. Curcumin inhibits thrombin to reduce P300-induced histone acetylation in the promoter region of TGF-β1, which is known to induce PD-L1 expression. Anti-PD-1 antibodies suppress the binding of PD-1 and PD-L1 to promote anticancer immune activity. Therefore, the combination of curcumin and anti-PD-1 antibodies showed better anticancer effects in vitro. The combination also slowed tumor growth and improved the TME in mouse model of HCC .
Proinflammatory cytokines in the TME inhibit antitumor immunity. IFN-γ and TNF-α are two key factors for triggering immunosuppression and resistance to immunosurveillance of T cells [85, 179,180,181].
IFN-γ exerts its critical role in cancer through the JAK/STAT1/interferon regulatory factor 1 (IRF-1) pathway . The IFN-γ pathway is important in inducing PD-L1 expression in the TME. Endogenous IFN-γ has been reported to upregulate PD-L1 expression in head and neck squamous cell carcinoma through the IFNAR1/STAT1 pathway, thereby promoting immune escape . JAK1/JAK2 inhibitor ruxolitinib inhibits the IFN-γ pathway, which enhances anti-PD-1 efficacy by downregulating PD-L1 expression in MDSCs .
Both cancer cells and IFN-γ-induced expression of PD-L1 are dependent on the mTOR pathway. The AKT/mTOR pathway promotes immune escape by driving PD-L1 expression . Therefore, combination treatment with mTOR inhibitors and ICIs may enhance the efficacies of immunotherapies.
NF-κB p65-induced COP9 signalosome 5 (CSN5) is essential for maintaining TNF-α-induced stability of PD-L1 in cancer cells. CSN5 inhibits the ubiquitination and degradation of PD-L1. By downregulating CSN5, curcumin enhances the sensitivity of cancer to anti-CTLA-4 treatment and the function of antitumor T cells by downregulating PD-L1 expression, thus alleviating cancer growth .
Intra-tumoral copper levels promoted PD-L1 expression at mRNA and protein levels in tumor cells. Copper chelator downregulates PD-L1 expression by inhibiting the response of cancer cells to proinflammatory cytokines such as IFN-γ, TNF-α and TNF-α/β. Copper-chelating drugs inhibits the expression of PD-L1 by downregulating phosphorylated STAT3, EGFR, AKT and GSK3β and mediates the ubiquitination and degradation of PD-L1 in cancer cells . Dietary composition also affects PD-L1 expression. Epigallocatechin gallate (EGCG), the most abundant ingredient in green tea, downregulates PD-L1 expression in NSCLC induced by IFN-γ and EGF .
TAM depletion and hypoxia alleviation synergistically reprogram the TME. This combination concurrently downregulates PD-L1 expression in tumor cells, decreases the levels of immunosuppressive cytokines such as IL-10 and TGF-β, elevates immunostimulatory IFN-γ, enhances the CTL response and boosts the memory response. TAM-targeted chemoimmunotherapy markedly inhibit cancer metastasis and recurrence .
In addition to the abovementioned mechanisms, other mechanisms are involved in the anticancer effects through regulation of PD-L1. Unique proline isomerase Pin1 drives immunosuppressive TME by influencing CAFs and induces lysosomal degradation of PD-L1. Inhibition of the Pin1 simultaneously blocks multiple cancer pathways, disrupts the immunosuppressive TME and upregulates the expression of PD-L1 and gemcitabine transporter ENT1, thus benefiting PDAC patients undergoing immunochemotherapy .
N6 methyladenosine (m6A) is an important posttranscriptional regulator. ALKBH5 is an m6A demethylase that coordinates PD-L1 expression in human intrahepatic cholangiocarcinoma (ICC). N6-methyladenosine sequencing (m6A-seq) confirmed that PD-L1 mRNA is the direct target of m6A modification, which is regulated by ALKBH5. ALKBH5 inhibits T cell expansion and cytotoxicity by stabilizing the expression level of PD-L1 in cancer cells .
Serotonin [5-hydroxytryptamine (5-HT)] is an inflammatory mediator associated with the proliferation and invasion of multiple types of cancer cells [248, 249]. Serotonin promoted expression of PD-L1 on cancer cells in vitro via serotonylation and its levels at metastatic sites of abdominal cancer were negatively correlated with the proportion of tumor-infiltrating cytotoxic T cells. Depletion of serotonin cargo enhanced CD8+ T cell infiltration and decreased PD-L1 expression. Pharmacological serotonin depletion enhances anticancer effects of PD-1 inhibitors in mice with colorectal and pancreatic cancer .
Preclinical models used in research about PD-1/PD-L1 blockade
The success of PD-1/PD-L1 blockade in cancer treatment is inseparable from the foundation laid by preclinical experiments. In preclinical research, the selection of tumor cells and animal models is critical to obtain clinically translational data. Therefore, we will briefly describe the tumor cells and animal tumor models used in preclinical studies on PD-1/PD-L1 interaction. PD-1/PD-L1 inhibitors have high response rates in melanoma relative to other cancer types. Lung cancer is currently the second most common cancer, and some PD-1/PD-L1 inhibitors have also achieved good therapeutic effects in specific lung cancer patients. Table 4 summarizes the representative cell lines and animal models for PD-1/PD-L1 interaction studies in melanoma and lung cancer. The information in the table indicates that many mouse and human tumor cells were used in in vitro experiments. For studies in mice, most experiments established xenograft models using mouse tumor cells in immunocompetent C57BL/6 mice and BALB/c mice. Other studies used NSG mice with/without human CD34+ human stem cell-engrafted to establish xenograft models of human tumor cells [250, 251]. However, one of the limitations of the xenograft model is that it is too far from the real process of tumorigenesis, and the conclusions obtained in those models cannot be better translated into clinical research. Therefore, the regulation of PD-1/PD-L1 signaling pathway has also been investigated using a transgenic mouse tumor model . Several studies have also established metastasis models by i.v. injection to study the therapeutic effect of PD-1/PD-L1 blockade on tumor metastasis [253, 254]. Most studies have examined the effects of modulating PD-1/PD-L1 in tumor therapy, some of which include the combination of PD-1/PD-L1 blockade with other therapeutic strategies [251, 255].
Organoids are tiny, self-organized three dimensional multicellular in vitro tissue construct that displays realistic micro-anatomy and mimics their corresponding in vivo organs. Such cultures have the ability to replicate much of the complexity of an organ and recapitulate certain functions of the represented organ . Reliable methods for predicting treatment response are urgently needed in clinical oncology. Cancer organoids can accurately reproduce important genetic and phenotypic characteristics of the tissue from which they are derived, tumor subtypes, and maintain intra- and inter-tumor heterogeneity, and thus have the potential to be used to predict individualized treatment response . In recent years, many studies have used cancer organoids, especially patient-derived cancer organoids (PDO) to conduct comprehensive studies of PD-1/PD-L1 interaction. Table 5 summarizes this aspect of research conducted in cancer organoids. Most cancer organoids were derived from cancer tissues of patients with gastrointestinal tumors. Organoid/immune cell co-cultures can model tumor-immune microenvironment. Most studies used cancer organoids to mimic the interaction of cancer cells with the human immune system in vitro. When conducting in vivo studies, NSG mice are required. After establishing tumor models in mice by orthotopic transplantation, these cancer organoids can predict the efficacy of PD-1/PD-L1 blockade as well as other treatment regimens [258,259,260,261]. These studies used organoids to investigate PD-1/PD-L1 interaction in various aspects, including testing the anticancer efficacy of PD-1/PD-L1 inhibitors [261,262,263], analyzing the regulation mechanism of PD-L1 expression [258, 259], finding strategies to enhance the therapeutic effect of PD-1/PD-L1 blockade [260, 264,265,266,267,268], finding new immune checkpoints . Through these studies, we can see that cancer organoids can be used to simulate the immune microenvironment in cancer patients, providing an effective tool for improving the efficacy of PD-1/PD-L1 blockade.
Adverse events of ICIs
Although ICIs induce the immune system to fight against cancer cells by activating T cells, they may also help to attack normal cells and thus result in immune-related adverse events (irAEs). The infiltration of immune cells, especially T cells, caused by combination treatment with anti-CTLA-4 and anti-PD-1/PD-L1 antibodies leads to irAEs.
Some irAEs caused by immunotherapy may be similar to AEs of other therapeutic strategies. However, similar AEs (e.g., diarrhea, enteritis, rashes and itching) can be caused by different mechanisms. The occurrence of irAEs is related to inflammatory responses, especially those mediated by CD8+ T cell activation. Other types of inflammatory cells such as Th17 may also be involved. An immunohistochemistry assay revealed the infiltration of CD4+ and CD8+ T cells in damaged skins and organs, and highly activated effector T cells are correlated with the incidence of AEs [29, 304,305,306]. Generally, irAEs are classified into organ-specific AEs (e.g., colitis, hepatitis and pneumonia), common AEs (e.g., fatigue, diarrhea and rashes) and others related to systemic inflammation. Most irAEs are mild to moderate, but serious or life-threatening irAEs have also occurred, with the highest fatality rates due to AEs in the nervous system and heart .
Compared with AEs caused by conventional chemotherapy, irAEs are characterized by delayed onset, long-term duration and different toxicity spectra. Pneumonia and arthralgia are the most common irAEs [29, 307,308,309,310]. The incidence of all-grade AEs caused by PD-1/PD-L1 inhibitors is lower than that of chemotherapy, and that of grade 3–4 AEs accounts for 7–13% with a relatively high safety [310,311,312]. Although the incidence of AEs increases in combination treatment, most of them are well tolerated [130, 313]. At present, management strategies for irAEs have been published, and most irAEs can be controlled or even reversed by withdrawal with or without corticosteroid hormone medication [309, 314].
Compared with those of conventional treatment, AEs caused by ICIs mainly affect the skin, endocrine system and lungs [315, 316]. Of the common ICIs, nivolumab is considered the safest, followed by atezolizumab, pembrolizumab, ipilimumab and tremelimumab. Their main AEs are summarized as follows: atezolizumab (hyperthyroidism, nausea and vomiting), nivolumab (endocrine toxicity), pembrolizumab (arthralgia, pneumonia and hepatotoxicity), ipilimumab (skin, gastrointestinal and kidney toxicity) and tremelimumab (rashes, diarrhea and fatigue). Taken together, these findings indicate that nivolumab is the safest ICI that is specifically suitable for lung cancer treatment. In conclusion, irAEs are insidious onset, lack specificity and have a wide spectrum of toxicity. Clinicians need to strengthen the management of irAEs from five aspects: prevention, assessment, examination, treatment and detection, so as to effectively control the disease.
Based on the regulatory mechanisms in T cells, PD-1/PD-L1 blockade has greatly advanced cancer treatment by enhancing the antitumor immune response. Its efficacy in the treatment of melanoma and NSCLC, in particular, is extraordinary, as it achieves long-term remission in a portion of cancer patients without recurrence.
Hot tumors identified by relevant biomarkers, such as T cell infiltration and PD-L1 expression, are closely linked with the clinical benefits of anti-PD-1/PD-L1 antibodies. In cold tumors, anti-CTLA-4 treatment creates a TME that is favorable to anti-PD-1/PD-L1 antibody treatment by recruiting T cells to target cancer lesions and inducing PD-L1 expression, which provides a rationale for combination therapy. Currently, great effort is directed to identifying predictive biomarkers for ICB.
PD-1/PD-L1 blockade has low response rates in many cancer patients due to innate and acquired resistance. Therefore, based on the resistance mechanism, PD-1/PD-L1 blockade combined with other treatment regimens is an effective strategy to improve anticancer efficacy and reduce side effects. Combining approved PD-1/PD-L1 inhibitors with other approved treatments may facilitate rapid approval of an effective combination. On the other hand, combining approved/investigational PD-1/PD-L1 inhibitors with other investigational treatment will lead to many breakthroughs. The expression of PD-L1 in TME also affects the effect of PD-1/PD-L1 blockade. This review introduces the factors affecting PD-L1 expression and strategies to regulate its expression. The success of PD-1/PD-L1 inhibitors in cancer therapy relies on extensive preclinical research. The selection of cell lines, animal strains and cancer models is critical for obtaining translational data. Therefore, this review describes the models used in preclinical studies of PD-1/PD-L1 interaction in melanoma and lung cancer. Notably, many studies have utilized cancer organoids to mimic the interaction of cancer cells with the human immune system in vitro, and these organoids are able to accurately replicate key genetic and phenotypic features of patient cancer tissue while maintaining heterogeneity. They can be used to simulate the immune microenvironment of cancer patients and provide an effective tool for improving PD-1/PD-L1 blockade.
PD-1/PD-L1 blockade and its combination therapy can control or even cure malignant diseases in the long term, providing new insights into cancer treatment. Specific agents or interventions can modulate the level of PD-1 and PD-L1, so as to exert a similar effect to ICIs. Owing to the inherent specificity, adaptability and memory of the immune system, researchers are able to continuously target and precisely kill cancer cells. The next goal of preclinical and clinical research is to find reasonable combinations of PD-1/PD-L1 blockade and other treatments to reduce toxic side effects, exert stronger anti-tumor immune responses and precisely kill cancer cells, so that cancer can become a type of curable chronic disease.
Availability of data and materials
Programmed cell death 1 receptor
Programmed cell death ligand 1
Cytotoxic T-lymphocyte-associated protein 4
Immune checkpoint blockade
Immune checkpoint inhibitors
Immunoreceptor tyrosine-based inhibitory motifs
Immunoreceptor tyrosine-based switch motifs
T cell receptor
Major histocompatibility complexes
Antigen presenting cell
B cell receptor
Non-small-cell lung cancer
Renal cell carcinoma
Effector T cells
Memory T cells
Regulatory T cells
Exhaustion T cells
Lymphocytic choriomeningitis virus
Transforming growth factor β
Interferon-sensitive responsive element
Tumor necrosis factor-α
Epithelial growth factor receptor
Epithelial growth factor
T cell acute lymphoblastic leukemia
Food and Drug Administration
Overall response rate
Median progression-free survival
Immunogenic cell death
Damage-associated molecular patterns
Myeloid-derived suppressor cells
Small-cell lung cancer
Triple negative breast cancer
Type I interferons
Stereotactic body radiation therapy
Breathing adapted radiotherapy
Main pathological response
Pathological complete remission
Tyrosine kinase inhibitors
Tumor infiltrating lymphocytes
DNA damage response
Poly ADP-ribose polymerase
Checkpoint kinase 1
Castration-resistant prostate cancer
Melanoma brain metastasis
Colony-stimulating factor 1 receptor
Tumor interstitial fluid pressure
Immune checkpoint therapy
Stimulator of interferon genes
Type I interferon
Adoptive cell therapy
Multistage sensitive nanocomplex
Extracellular signal-regulated kinases 1/2
Extracellular signal-regulated kinases 1/2
Endoplasmic reticulum-associated proteins
Interferon regulatory factor 1
COP9 signalosome 5
Pancreatic ductal adenocarcinoma
Ghosh C, Luong G, Sun Y. A snapshot of the PD-1/PD-L1 pathway. J Cancer. 2021;12:2735–46.
Cao L, Prithviraj P, Shrestha R, Sharma R, Anaka M, Bridle KR, et al. Prognostic role of immune checkpoint regulators in cholangiocarcinoma: a pilot study. J Clin Med. 2021;10:2191.
Hossain MA, Liu G, Dai B, Si Y, Yang Q, Wazir J, et al. Reinvigorating exhausted CD8(+) cytotoxic T lymphocytes in the tumor microenvironment and current strategies in cancer immunotherapy. Med Res Rev. 2021;41:156–201.
Pitt JM, Vetizou M, Daillere R, Roberti MP, Yamazaki T, Routy B, et al. Resistance mechanisms to immune-checkpoint blockade in cancer: tumor-intrinsic and -extrinsic factors. Immunity. 2016;44:1255–69.
Sun S, Xu L, Zhang X, Pang L, Long Z, Deng C, et al. Systematic assessment of transcriptomic biomarkers for immune checkpoint blockade response in cancer immunotherapy. Cancers (Basel). 2021;13:1639.
Sehrawat N, Yadav M, Singh M, Kumar V, Sharma VR, Sharma AK. Probiotics in microbiome ecological balance providing a therapeutic window against cancer. Semin Cancer Biol. 2021;70:24–36.
Budhu S, Giese R, Gupta A, Fitzgerald K, Zappasodi R, Schad S, et al. Targeting phosphatidylserine enhances the anti-tumor response to tumor-directed radiation therapy in a preclinical model of melanoma. Cell Rep. 2021;34:108620.
Kim HJ, Cantor H, Cosmopoulos K. Overcoming immune checkpoint blockade resistance via EZH2 inhibition. Trends Immunol. 2020;41:948–63.
Patel SA, Minn AJ. Combination cancer therapy with immune checkpoint blockade: mechanisms and strategies. Immunity. 2018;48:417–33.
Colom B, Herms A, Hall MWJ, Dentro SC, King C, Sood RK, et al. Mutant clones in normal epithelium outcompete and eliminate emerging tumours. Nature. 2021;598:510–4.
Baggiolini A, Callahan SJ, Montal E, Weiss JM, Trieu T, Tagore MM, et al. Developmental chromatin programs determine oncogenic competence in melanoma. Science. 2021;373:eabc1048.
Ho WJ, Wood LD. Opposing roles of the immune system in tumors. Science. 2021;373:1306–7.
Sato E, Olson SH, Ahn J, Bundy B, Nishikawa H, Qian F, et al. Intraepithelial CD8+ tumor-infiltrating lymphocytes and a high CD8+/regulatory T cell ratio are associated with favorable prognosis in ovarian cancer. Proc Natl Acad Sci USA. 2005;102:18538–43.
Chen DS, Mellman I. Oncology meets immunology: the cancer-immunity cycle. Immunity. 2013;39:1–10.
Wang M, Liu Y, Cheng Y, Wei Y, Wei X. Immune checkpoint blockade and its combination therapy with small-molecule inhibitors for cancer treatment. Biochim Biophys Acta Rev Cancer. 2019;1871:199–224.
Ishida Y, Agata Y, Shibahara K, Honjo T. Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death. EMBO J. 1992;11:3887–95.
Filippone A, Lanza M, Mannino D, Raciti G, Colarossi C, Sciacca D, et al. PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression. Cancer Immunol Immunother. 2022.
Sharpe AH, Wherry EJ, Ahmed R, Freeman GJ. The function of programmed cell death 1 and its ligands in regulating autoimmunity and infection. Nat Immunol. 2007;8:239–45.
Tarhini AA, Zahoor H, Yearley JH, Gibson C, Rahman Z, Dubner R, et al. Tumor associated PD-L1 expression pattern in microscopically tumor positive sentinel lymph nodes in patients with melanoma. J Transl Med. 2015;13:319.
Laurent C, Charmpi K, Gravelle P, Tosolini M, Franchet C, Ysebaert L, et al. Several immune escape patterns in non-Hodgkin’s lymphomas. Oncoimmunology. 2015;4:e1026530.
Said EA, Dupuy FP, Trautmann L, Zhang Y, Shi Y, El-Far M, et al. Programmed death-1-induced interleukin-10 production by monocytes impairs CD4+ T cell activation during HIV infection. Nat Med. 2010;16:452–9.
Zak KM, Grudnik P, Magiera K, Domling A, Dubin G, Holak TA. Structural biology of the immune checkpoint receptor PD-1 and its ligands PD-L1/PD-L2. Structure. 2017;25:1163–74.
Lee HT, Lee SH, Heo YS. Molecular interactions of antibody drugs targeting PD-1, PD-L1, and CTLA-4 in immuno-oncology. Molecules. 2019;24:1190.
Guzik K, Tomala M, Muszak D, Konieczny M, Hec A, Blaszkiewicz U, et al. Development of the inhibitors that target the PD-1/PD-L1 interaction-a brief look at progress on small molecules, peptides and macrocycles. Molecules. 2019;24:2071.
Francisco LM, Sage PT, Sharpe AH. The PD-1 pathway in tolerance and autoimmunity. Immunol Rev. 2010;236:219–42.
Shinohara T, Taniwaki M, Ishida Y, Kawaichi M, Honjo T. Structure and chromosomal localization of the human PD-1 gene (PDCD1). Genomics. 1994;23:704–6.
Dong H, Zhu G, Tamada K, Chen L. B7–H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion. Nat Med. 1999;5:1365–2136.
Tseng SY, Otsuji M, Gorski K, Huang X, Slansky JE, Pai SI, et al. B7-DC, a new dendritic cell molecule with potent costimulatory properties for T cells. J Exp Med. 2001;193:839–46.
Keir ME, Butte MJ, Freeman GJ, Sharpe AH. PD-1 and its ligands in tolerance and immunity. Annu Rev Immunol. 2008;26:677–704.
Cai J, Wang D, Zhang G, Guo X. The role of PD-1/PD-L1 axis in treg development and function: implications for cancer immunotherapy. Onco Targets Ther. 2019;12:8437–45.
Jiang X, Wang J, Deng X, Xiong F, Ge J, Xiang B, et al. Role of the tumor microenvironment in PD-L1/PD-1-mediated tumor immune escape. Mol Cancer. 2019;18:10.
Hofmeyer KA, Jeon H, Zang X. The PD-1/PD-L1 (B7–H1) pathway in chronic infection-induced cytotoxic T lymphocyte exhaustion. J Biomed Biotechnol. 2011;2011:1–9.
Patsoukis N, Li L, Sari D, Petkova V, Boussiotis VA. PD-1 increases PTEN phosphatase activity while decreasing PTEN protein stability by inhibiting casein kinase 2. Mol Cell Biol. 2013;33:3091–8.
Wartewig T, Kurgyis Z, Keppler S, Pechloff K, Hameister E, Ollinger R, et al. PD-1 is a haploinsufficient suppressor of T cell lymphomagenesis. Nature. 2017;552:121–5.
Seto T, Sam D, Pan M. Mechanisms of primary and secondary resistance to immune checkpoint inhibitors in cancer. Med Sci (Basel). 2019;7:14.
Jubel JM, Barbati ZR, Burger C, Wirtz DC, Schildberg FA. The role of PD-1 in acute and chronic infection. Front Immunol. 2020;11:487.
Riella LV, Paterson AM, Sharpe AH, Chandraker A. Role of the PD-1 pathway in the immune response. Am J Transplant. 2012;12:2575–87.
Sakuishi K, Apetoh L, Sullivan JM, Blazar BR, Kuchroo VK, Anderson AC. Targeting Tim-3 and PD-1 pathways to reverse T cell exhaustion and restore anti-tumor immunity. J Exp Med. 2010;207:2187–94.
Sun S, Fei X, Mao Y, Wang X, Garfield DH, Huang O, et al. PD-1(+) immune cell infiltration inversely correlates with survival of operable breast cancer patients. Cancer Immunol Immunother. 2014;63:395–406.
Muenst S, Soysal SD, Gao F, Obermann EC, Oertli D, Gillanders WE. The presence of programmed death 1 (PD-1)-positive tumor-infiltrating lymphocytes is associated with poor prognosis in human breast cancer. Breast Cancer Res Treat. 2013;139:667–76.
Hawkes EA, Grigg A, Chong G. Programmed cell death-1 inhibition in lymphoma. Lancet Oncol. 2015;16:e234–45.
Velcheti V, Schalper KA, Carvajal DE, Anagnostou VK, Syrigos KN, Sznol M, et al. Programmed death ligand-1 expression in non-small cell lung cancer. Lab Investig. 2014;94:107–16.
Boland JM, Kwon ED, Harrington SM, Wampfler JA, Tang H, Yang P, et al. Tumor B7–H1 and B7–H3 expression in squamous cell carcinoma of the lung. Clin Lung Cancer. 2013;14:157–63.
Spranger S, Spaapen RM, Zha Y, Williams J, Meng Y, Ha TT, et al. Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells. Sci Transl Med. 2013;5:200ra116.
Thompson RH, Kuntz SM, Leibovich BC, Dong H, Lohse CM, Webster WS, et al. Tumor B7–H1 is associated with poor prognosis in renal cell carcinoma patients with long-term follow-up. Cancer Res. 2006;66:3381–5.
Sfanos KS, Bruno TC, Meeker AK, De Marzo AM, Isaacs WB, Drake CG. Human prostate-infiltrating CD8+ T lymphocytes are oligoclonal and PD-1+. Prostate. 2009;69:1694–703.
Soliman H, Khalil F, Antonia S. PD-L1 expression is increased in a subset of basal type breast cancer cells. PLoS ONE. 2014;9:e88557.
Liu Y, Carlsson R, Ambjorn M, Hasan M, Badn W, Darabi A, et al. PD-L1 expression by neurons nearby tumors indicates better prognosis in glioblastoma patients. J Neurosci. 2013;33:14231–45.
Efremova M, Rieder D, Klepsch V, Charoentong P, Finotello F, Hackl H, et al. Targeting immune checkpoints potentiates immunoediting and changes the dynamics of tumor evolution. Nat Commun. 2018;9:32.
Wherry EJ. T cell exhaustion. Nat Immunol. 2011;12:492–9.
Chen G, Huang AC, Zhang W, Zhang G, Wu M, Xu W, et al. Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response. Nature. 2018;560:382–6.
Zhou J, Mahoney KM, Giobbie-Hurder A, Zhao F, Lee S, Liao X, et al. Soluble PD-L1 as a biomarker in malignant melanoma treated with checkpoint blockade. Cancer Immunol Res. 2017;5:480–92.
Theodoraki M-N, Yerneni SS, Hoffmann TK, Gooding WE, Whiteside TL. Clinical significance of PD-L1+ exosomes in plasma of head and neck cancer patients. Clin Cancer Res. 2018;24:896–905.
Chen DS, Mellman I. Elements of cancer immunity and the cancer-immune set point. Nature. 2017;541:321–30.
Daskivich TJ, Belldegrun A. Words of wisdom. Re: safety, activity, and immune correlates of anti-PD-1 antibody in cancer. Eur Urol. 2015;67:816–7.
Brahmer JR, Tykodi SS, Chow LQ, Hwu WJ, Topalian SL, Hwu P, et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med. 2012;366:2455–65.
Topalian SL. Targeting immune checkpoints in cancer therapy. JAMA. 2017;318:1647–8.
Liu B, Song Y, Liu D. Recent development in clinical applications of PD-1 and PD-L1 antibodies for cancer immunotherapy. J Hematol Oncol. 2017;10:174.
Wei F, Wu Y, Tang L, He Y, Shi L, Xiong F, et al. BPIFB1 (LPLUNC1) inhibits migration and invasion of nasopharyngeal carcinoma by interacting with VTN and VIM. Br J Cancer. 2018;118:233–47.
Wang JP, Tang YY, Fan CM, Guo C, Zhou YH, Li Z, et al. The role of exosomal non-coding RNAs in cancer metastasis. Oncotarget. 2017;9:12487–502.
Wang M, Zhao J, Zhang L, Wei F, Lian Y, Wu Y, et al. Role of tumor microenvironment in tumorigenesis. J Cancer. 2017;8:761–73.
Shao C, Yang F, Miao S, Liu W, Wang C, Shu Y, et al. Role of hypoxia-induced exosomes in tumor biology. Mol Cancer. 2018;17:120.
Majo S, Auguste P. The Yin and Yang of discoidin domain receptors (DDRs): implications in tumor growth and metastasis development. Cancers (Basel). 2021;13:1725.
Selenko-Gebauer N, Majdic O, Szekeres A, Hofler G, Guthann E, Korthauer U, et al. B7–H1 (programmed death-1 ligand) on dendritic cells is involved in the induction and maintenance of T cell anergy. J Immunol. 2003;170:3637–44.
Tsushima F, Yao S, Shin T, Flies A, Flies S, Xu H, et al. Interaction between B7–H1 and PD-1 determines initiation and reversal of T-cell anergy. Blood. 2007;110:180–5.
Bengsch B, Johnson AL, Kurachi M, Odorizzi PM, Pauken KE, Attanasio J, et al. Bioenergetic insufficiencies due to metabolic alterations regulated by the inhibitory receptor PD-1 are an early driver of CD8(+) T cell exhaustion. Immunity. 2016;45:358–73.
Barber DL, Wherry EJ, Masopust D, Zhu B, Allison JP, Sharpe AH, et al. Restoring function in exhausted CD8 T cells during chronic viral infection. Nature. 2006;439:682–7.
Francisco LM, Salinas VH, Brown KE, Vanguri VK, Freeman GJ, Kuchroo VK, et al. PD-L1 regulates the development, maintenance, and function of induced regulatory T cells. J Exp Med. 2009;206:3015–29.
Yao S, Wang S, Zhu Y, Luo L, Zhu G, Flies S, et al. PD-1 on dendritic cells impedes innate immunity against bacterial infection. Blood. 2009;113:5811–8.
Wei SC, Duffy CR, Allison JP. Fundamental mechanisms of immune checkpoint blockade therapy. Cancer Discov. 2018;8:1069–86.
Azuma T, Yao S, Zhu G, Flies AS, Flies SJ, Chen L. B7–H1 is a ubiquitous antiapoptotic receptor on cancer cells. Blood. 2008;111:3635–43.
Kleffel S, Posch C, Barthel SR, Mueller H, Schlapbach C, Guenova E, et al. Melanoma cell-intrinsic PD-1 receptor functions promote tumor growth. Cell. 2015;162:1242–56.
Rekik R, Belhadj Hmida N, Ben Hmid A, Zamali I, Kammoun N, Ben AM. PD-1 induction through TCR activation is partially regulated by endogenous TGF-beta. Cell Mol Immunol. 2015;12:648–9.
Heyner M, Schreier S, Kröger A. The brain-immune cells axis controls tissue specific immunopathology. Cell Mol Immunol. 2019;16:101–3.
Freeman GJ, Long AJ, Iwai Y, Bourque K, Chernova T, Nishimura H, et al. Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation. J Exp Med. 2000;192:1027–34.
Bally AP, Tang Y, Lee JT, Barwick BG, Martinez R, Evavold BD, et al. Conserved region C functions to regulate PD-1 expression and subsequent CD8 T cell memory. J Immunol. 2017;198:205–17.
Bommarito D, Hall C, Taams LS, Corrigall VM. Inflammatory cytokines compromise programmed cell death-1 (PD-1)-mediated T cell suppression in inflammatory arthritis through up-regulation of soluble PD-1. Clin Exp Immunol. 2017;188:455–66.
Cho HY, Lee SW, Seo SK, Choi IW, Choi I, Lee SW. Interferon-sensitive response element (ISRE) is mainly responsible for IFN-alpha-induced upregulation of programmed death-1 (PD-1) in macrophages. Biochim Biophys Acta. 2008;1779:811–9.
Terawaki S, Chikuma S, Shibayama S, Hayashi T, Yoshida T, Okazaki T, et al. IFN-alpha directly promotes programmed cell death-1 transcription and limits the duration of T cell-mediated immunity. J Immunol. 2011;186:2772–9.
Deng X, Xiong F, Li X, Xiang B, Li Z, Wu X, et al. Application of atomic force microscopy in cancer research. J Nanobiotechnol. 2018;16:102.
Weber EW, Parker KR, Sotillo E, Lynn RC, Anbunathan H, Lattin J, et al. Transient rest restores functionality in exhausted CAR-T cells through epigenetic remodeling. Science. 2021;372:eaba1786.
Spaccarelli N, Rook AH. The use of interferons in the treatment of cutaneous T-cell lymphoma. Dermatol Clin. 2015;33:731–45.
Mandai M, Hamanishi J, Abiko K, Matsumura N, Baba T, Konishi I. Dual faces of IFNγ in cancer progression: a role of PD-L1 induction in the determination of pro- and antitumor immunity. Clin Cancer Res. 2016;22:2329–34.
Bo H, Fan L, Li J, Liu Z, Zhang S, Shi L, et al. High expression of lncRNA AFAP1-AS1 promotes the progression of colon cancer and predicts poor prognosis. J Cancer. 2018;9:4677–83.
Wang X, Yang L, Huang F, Zhang Q, Liu S, Ma L, et al. Inflammatory cytokines IL-17 and TNF-α up-regulate PD-L1 expression in human prostate and colon cancer cells. Immunol Lett. 2017;184:7–14.
Yee D, Shah KM, Coles MC, Sharp TV, Lagos D. MicroRNA-155 induction via TNF-alpha and IFN-gamma suppresses expression of programmed death ligand-1 (PD-L1) in human primary cells. J Biol Chem. 2017;292:20683–93.
Zhang N, Zeng Y, Du W, Zhu J, Shen D, Liu Z, et al. The EGFR pathway is involved in the regulation of PD-L1 expression via the IL-6/JAK/STAT3 signaling pathway in EGFR-mutated non-small cell lung cancer. Int J Oncol. 2016;49:1360–8.
Shen MJ, Xu LJ, Yang L, Tsai Y, Keng PC, Chen Y, et al. Radiation alters PD-L1/NKG2D ligand levels in lung cancer cells and leads to immune escape from NK cell cytotoxicity via IL-6-MEK/Erk signaling pathway. Oncotarget. 2017;8:80506–20.
Xu L, Chen X, Shen M, Yang DR, Fang L, Weng G, et al. Inhibition of IL-6-JAK/Stat3 signaling in castration-resistant prostate cancer cells enhances the NK cell-mediated cytotoxicity via alteration of PD-L1/NKG2D ligand levels. Mol Oncol. 2018;12:269–86.
Eriksson E, Milenova I, Wenthe J, Moreno R, Alemany R, Loskog A. IL-6 signaling blockade during CD40-mediated immune activation favors antitumor factors by reducing TGF-beta, collagen type I, and PD-L1/PD-1. J Immunol. 2019;202:787–98.
Wang Y, Hu J, Wang Y, Ye W, Zhang X, Ju H, et al. EGFR activation induced Snail-dependent EMT and myc-dependent PD-L1 in human salivary adenoid cystic carcinoma cells. Cell Cycle. 2018;17:1457–70.
Wang J, Jia Y, Zhao S, Zhang X, Wang X, Han X, et al. BIN1 reverses PD-L1-mediated immune escape by inactivating the c-MYC and EGFR/MAPK signaling pathways in non-small cell lung cancer. Oncogene. 2017;36:6235–43.
Li J, Gu J. PD-L1 expression and EGFR status in advanced non-small-cell lung cancer patients receiving PD-1/PD-L1 inhibitors: a meta-analysis. Future Oncol (Lond, Engl). 2019;15:1667–78.
Casey SC, Tong L, Li Y, Do R, Walz S, Fitzgerald KN, et al. MYC regulates the antitumor immune response through CD47 and PD-L1. Science (New York, NY). 2016;352:227–31.
Mazzarella L, Morganti S, Marra A, Trapani D, Tini G, Pelicci P, et al. Master protocols in immuno-oncology: do novel drugs deserve novel designs? J Immunother Cancer. 2020;8:e000475.
Akbay EA, Koyama S, Carretero J, Altabef A, Tchaicha JH, Christensen CL, et al. Activation of the PD-1 pathway contributes to immune escape in EGFR-driven lung tumors. Cancer Discov. 2013;3:1355–63.
Glorieux C, Xia X, He YQ, Hu Y, Cremer K, Robert A, et al. Regulation of PD-L1 expression in K-ras-driven cancers through ROS-mediated FGFR1 signaling. Redox Biol. 2021;38:101780.
Valadi H, Ekstrom K, Bossios A, Sjostrand M, Lee JJ, Lotvall JO. Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells. Nat Cell Biol. 2007;9:654–9.
Lo Cicero A, Stahl PD, Raposo G. Extracellular vesicles shuffling intercellular messages: for good or for bad. Curr Opin Cell Biol. 2015;35:69–77.
Gu W, Wang L, Wu Y, Liu JP. Undo the brake of tumour immune tolerance with antibodies, peptide mimetics and small molecule compounds targeting PD-1/PD-L1 checkpoint at different locations for acceleration of cytotoxic immunity to cancer cells. Clin Exp Pharmacol Physiol. 2019;46:105–15.
Gabrusiewicz K, Li X, Wei J, Hashimoto Y, Marisetty AL, Ott M, et al. Glioblastoma stem cell-derived exosomes induce M2 macrophages and PD-L1 expression on human monocytes. Oncoimmunology. 2018;7:e1412909.
Haderk F, Schulz R, Iskar M, Cid LL, Worst T, Willmund KV, et al. Tumor-derived exosomes modulate PD-L1 expression in monocytes. Sci Immunol. 2017;2:eaah5509.
Latchman Y, Wood CR, Chernova T, Chaudhary D, Borde M, Chernova I, et al. PD-L2 is a second ligand for PD-1 and inhibits T cell activation. Nat Immunol. 2001;2:261–8.
Viricel C, Ahmed M, Barakat K. Human PD-1 binds differently to its human ligands: a comprehensive modeling study. J Mol Graph Model. 2015;57:131–42.
Philips EA, Garcia-Espana A, Tocheva AS, Ahearn IM, Adam KR, Pan R, et al. The structural features that distinguish PD-L2 from PD-L1 emerged in placental mammals. J Biol Chem. 2020;295:4372–80.
Yearley JH, Gibson C, Yu N, Moon C, Murphy E, Juco J, et al. PD-L2 expression in human tumors: relevance to anti-PD-1 therapy in cancer. Clin Cancer Res. 2017;23:3158–67.
Messal N, Serriari NE, Pastor S, Nunès JA, Olive D. PD-L2 is expressed on activated human T cells and regulates their function. Mol Immunol. 2011;48:2214–9.
Zhang Y, Chung Y, Bishop C, Daugherty B, Chute H, Holst P, et al. Regulation of T cell activation and tolerance by PDL2. Proc Natl Acad Sci U S A. 2006;103:11695–700.
Liu X, Gao JX, Wen J, Yin L, Li O, Zuo T, et al. B7DC/PDL2 promotes tumor immunity by a PD-1-independent mechanism. J Exp Med. 2003;197:1721–30.
Saunders PA, Hendrycks VR, Lidinsky WA, Woods ML. PD-L2:PD-1 involvement in T cell proliferation, cytokine production, and integrin-mediated adhesion. Eur J Immunol. 2005;35:3561–9.
Bardhan K, Anagnostou T, Boussiotis VA. The PD1:PD-L1/2 pathway from discovery to clinical implementation. Front Immunol. 2016;7:550.
Chinai JM, Janakiram M, Chen F, Chen W, Kaplan M, Zang X. New immunotherapies targeting the PD-1 pathway. Trends Pharmacol Sci. 2015;36:587–95.
Qin W, Hu L, Zhang X, Jiang S, Li J, Zhang Z, et al. The diverse function of PD-1/PD-L pathway beyond cancer. Front Immunol. 2019;10:2298.
Kane LP, Weiss A. The PI-3 kinase/Akt pathway and T cell activation: pleiotropic pathways downstream of PIP3. Immunol Rev. 2003;192:7–20.
Marasco M, Berteotti A, Weyershaeuser J, Thorausch N, Sikorska J, Krausze J, et al. Molecular mechanism of SHP2 activation by PD-1 stimulation. Sci Adv. 2020;6:eaay4458.
Chemnitz JM, Parry RV, Nichols KE, June CH, Riley JL. SHP-1 and SHP-2 associate with immunoreceptor tyrosine-based switch motif of programmed death 1 upon primary human T cell stimulation, but only receptor ligation prevents T cell activation. J Immunol. 2004;173:945–54.
Marcq E, Pauwels P, van Meerbeeck JP, Smits EL. Targeting immune checkpoints: new opportunity for mesothelioma treatment? Cancer Treat Rev. 2015;41:914–24.
Villanueva MT. Immunotherapy: searching in the immune checkpoint black box. Nat Rev Cancer. 2017;17:511.
Nishino M, Ramaiya NH, Hatabu H, Hodi FS. Monitoring immune-checkpoint blockade: response evaluation and biomarker development. Nat Rev Clin Oncol. 2017;14:655–68.
Galon J, Costes A, Sanchez-Cabo F, Kirilovsky A, Mlecnik B, Lagorce-Pages C, et al. Type, density, and location of immune cells within human colorectal tumors predict clinical outcome. Science. 2006;313:1960–4.
Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med. 2012;366:2443–54.
Llosa NJ, Cruise M, Tam A, Wicks EC, Hechenbleikner EM, Taube JM, et al. The vigorous immune microenvironment of microsatellite instable colon cancer is balanced by multiple counter-inhibitory checkpoints. Cancer Discov. 2015;5:43–51.
Kroemer G, Galluzzi L, Zitvogel L, Fridman WH. Colorectal cancer: the first neoplasia found to be under immunosurveillance and the last one to respond to immunotherapy? Oncoimmunology. 2015;4:e1058597.
Schoenfeld AJ, Hellmann MD. Acquired resistance to immune checkpoint inhibitors. Cancer Cell. 2020;37:443–55.
Gettinger S, Choi J, Hastings K, Truini A, Datar I, Sowell R, et al. Impaired HLA class I antigen processing and presentation as a mechanism of acquired resistance to immune checkpoint inhibitors in lung cancer. Cancer Discov. 2017;7:1420–35.
Gao J, Shi LZ, Zhao H, Chen J, Xiong L, He Q, et al. Loss of IFN-gamma pathway genes in tumor cells as a mechanism of resistance to anti-CTLA-4 therapy. Cell. 2016;167:397-404.e9.
Rosenthal R, Cadieux EL, Salgado R, Bakir MA, Moore DA, Hiley CT, et al. Neoantigen-directed immune escape in lung cancer evolution. Nature. 2019;567:479–85.
Minn AJ, Wherry EJ. Combination Cancer Therapies With Immune Checkpoint Blockade: Convergence On Interferon Signaling. Cell. 2016;165:272–5.
Zhou X, Yao Z, Bai H, Duan J, Wang Z, Wang X, et al. Treatment-related adverse events of PD-1 and PD-L1 inhibitor-based combination therapies in clinical trials: a systematic review and meta-analysis. Lancet Oncol. 2021;22:1265–74.
Gandhi L, Rodriguez-Abreu D, Gadgeel S, Esteban E, Felip E, De Angelis F, et al. Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer. N Engl J Med. 2018;378:2078–92.
Galon J, Bruni D. Approaches to treat immune hot, altered and cold tumours with combination immunotherapies. Nat Rev Drug Discov. 2019;18:197–218.
Warner AB, Postow MA. Combination controversies: checkpoint inhibition alone or in combination for the treatment of melanoma? Oncology (Williston Park). 2018;32:228–34.
Overman MJ, Lonardi S, Wong KY, Lenz HJ, Gelsomino F, Aglietta M, et al. Nivolumab plus Ipilimumab Achieves Responses in dMMR/MSI-H Tumors. Cancer Discov. 2018;8:263.
Vacchelli E, Ma Y, Baracco EE, Sistigu A, Enot DP, Pietrocola F, et al. Chemotherapy-induced antitumor immunity requires formyl peptide receptor 1. Science. 2015;350:972–8.
Steven A, Fisher SA, Robinson BW. Immunotherapy for lung cancer. Respirology. 2016;21:821–33.
Cascone T, William WN Jr, Weissferdt A, Leung CH, Lin HY, Pataer A, et al. Neoadjuvant nivolumab or nivolumab plus ipilimumab in operable non-small cell lung cancer: the phase 2 randomized NEOSTAR trial. Nat Med. 2021;27:504–14.
Passaro A, Attili I, de Marinis F. CheckMate 9LA: broadening treatment options for patients with non-small-cell lung cancer. Lancet Oncol. 2021;22:157–9.
The International Association for the Study of Lung Cancer (IASLC), Phase III POSEIDON Trial Shows Positive Results for Patients Taking Chemotherapy Plus Durvalumab and Tremelimumab. https://www.iaslc.org/iaslc-news/press-release/phase-iii-poseidon-trial-shows-positive-resultspatients-taking. 2021. Accessed 19 Feb 2022.
Doki Y, Ajani JA, Kato K, Xu J, Wyrwicz L, Motoyama S, et al. Nivolumab combination therapy in advanced esophageal squamous-cell carcinoma. N Engl J Med. 2022;386:449–62.
Tawbi HA, Forsyth PA, Hodi FS, Algazi AP, Hamid O, Lao CD, et al. Long-term outcomes of patients with active melanoma brain metastases treated with combination nivolumab plus ipilimumab (CheckMate 204): final results of an open-label, multicentre, phase 2 study. Lancet Oncol. 2021;22:1692–704.
O'Malley DM, Neffa M, Monk BJ, Melkadze T, Huang M, Kryzhanivska A, et al. Dual PD-1 and CTLA-4 checkpoint blockade using balstilimab and zalifrelimab combination as second-line treatment for advanced cervical cancer: an open-label phase II study. J Clin Oncol. 2021:Jco2102067.
Galluzzi L, Buque A, Kepp O, Zitvogel L, Kroemer G. Immunogenic cell death in cancer and infectious disease. Nat Rev Immunol. 2017;17:97–111.
Apetoh L, Ghiringhelli F, Tesniere A, Criollo A, Ortiz C, Lidereau R, et al. The interaction between HMGB1 and TLR4 dictates the outcome of anticancer chemotherapy and radiotherapy. Immunol Rev. 2007;220:47–59.
Vincent J, Mignot G, Chalmin F, Ladoire S, Bruchard M, Chevriaux A, et al. 5-Fluorouracil selectively kills tumor-associated myeloid-derived suppressor cells resulting in enhanced T cell-dependent antitumor immunity. Cancer Res. 2010;70:3052–61.
Wang W, Kryczek I, Dostal L, Lin H, Tan L, Zhao L, et al. Effector T cells abrogate stroma-mediated chemoresistance in ovarian cancer. Cell. 2016;165:1092–105.
Galluzzi L, Buque A, Kepp O, Zitvogel L, Kroemer G. Immunological effects of conventional chemotherapy and targeted anticancer agents. Cancer Cell. 2015;28:690–714.
Mathios D, Kim JE, Mangraviti A, Phallen J, Park CK, Jackson CM, et al. Anti-PD-1 antitumor immunity is enhanced by local and abrogated by systemic chemotherapy in GBM. Sci Transl Med. 2016;8:370ra180.
Langer CJ, Gadgeel SM, Borghaei H, Papadimitrakopoulou VA, Patnaik A, Powell SF, et al. Carboplatin and pemetrexed with or without pembrolizumab for advanced, non-squamous non-small-cell lung cancer: a randomised, phase 2 cohort of the open-label KEYNOTE-021 study. Lancet Oncol. 2016;17:1497–508.
Schmid P, Adams S, Rugo HS, Schneeweiss A, Barrios CH, Iwata H, et al. Atezolizumab and nab-paclitaxel in advanced triple-negative breast cancer. N Engl J Med. 2018;379:2108–21.
Miles D, Gligorov J, Andre F, Cameron D, Schneeweiss A, Barrios C, et al. Primary results from IMpassion131, a double-blind, placebo-controlled, randomised phase III trial of first-line paclitaxel with or without atezolizumab for unresectable locally advanced/metastatic triple-negative breast cancer. Ann Oncol. 2021;32:994–1004.
Zhang Y, Chen H, Mo H, Hu X, Gao R, Zhao Y, et al. Single-cell analyses reveal key immune cell subsets associated with response to PD-L1 blockade in triple-negative breast cancer. Cancer Cell. 2021;39(12):1578–93.
Yang Q, Shi G, Chen X, Lin Y, Cheng L, Jiang Q, et al. Nanomicelle protects the immune activation effects of Paclitaxel and sensitizes tumors to anti-PD-1 Immunotherapy. Theranostics. 2020;10:8382–99.
Paz-Ares L, Vicente D, Tafreshi A, Robinson A, Soto Parra H, Mazieres J, et al. A randomized, placebo-controlled trial of pembrolizumab plus chemotherapy in patients with metastatic squamous NSCLC: protocol-specified final analysis of KEYNOTE-407. J Thorac Oncol. 2020;15:1657–69.
Felip E, Altorki N, Zhou C, Csőszi T, Vynnychenko I, Goloborodko O, et al. Adjuvant atezolizumab after adjuvant chemotherapy in resected stage IB-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase 3 trial. Lancet (London, England). 2021;398:1344–57.
Provencio M, Nadal E, Insa A, García-Campelo MR, Casal-Rubio J, Dómine M, et al. Neoadjuvant chemotherapy and nivolumab in resectable non-small-cell lung cancer (NADIM): an open-label, multicentre, single-arm, phase 2 trial. Lancet Oncol. 2020;21:1413–22.
Jabbour SK, Lee KH, Frost N, Breder V, Kowalski DM, Pollock T, et al. Pembrolizumab plus concurrent chemoradiation therapy in patients with unresectable, locally advanced, stage III non-small cell lung cancer: the phase 2 KEYNOTE-799 nonrandomized trial. JAMA Oncol. 2021;7:1–9.
Janjigian YY, Kawazoe A, Yanez P, Li N, Lonardi S, Kolesnik O, et al. The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer. Nature. 2021;600:727–30.
Zhao JJ, Yap DWT, Chan YH, Tan BKJ, Teo CB, Syn NL, et al. Low programmed death-ligand 1-expressing subgroup outcomes of first-line immune checkpoint inhibitors in gastric or esophageal adenocarcinoma. J Clin Oncol. 2022;40:392–402.
Zhou C, Wang Z, Sun Y, Cao L, Ma Z, Wu R, et al. Sugemalimab versus placebo, in combination with platinum-based chemotherapy, as first-line treatment of metastatic non-small-cell lung cancer (GEMSTONE-302): interim and final analyses of a double-blind, randomised, phase 3 clinical trial. Lancet Oncol. 2022;23:220–33.
Mai HQ, Chen QY, Chen D, Hu C, Yang K, Wen J, et al. Publisher Correction: Toripalimab or placebo plus chemotherapy as first-line treatment in advanced nasopharyngeal carcinoma: a multicenter randomized phase 3 trial. Nat Med. 2022;28:214.
Nishio M, Barlesi F, West H, Ball S, Bordoni R, Cobo M, et al. Atezolizumab plus chemotherapy for first-line treatment of nonsquamous NSCLC: results from the randomized phase 3 IMpower132 trial. J Thorac Oncol. 2021;16:653–64.
Kim S, Sanders PD, Weihe E, Purcell T, Kato S, Patel S, et al. Analysis of immune correlates using anti-PD-1 checkpoint blockade immunotherapy combined with stereotactic body radiation therapy. Int J Radiat Oncol Biol Phys. 2017;99:E602–3.
Gong X, Li X, Jiang T, Xie H, Zhu Z, Zhou F, et al. Combined radiotherapy and anti-PD-L1 antibody synergistically enhances antitumor effect in non-small cell lung cancer. J Thorac Oncol. 2017;12:1085–97.
Vanneste BGL, Van Limbergen EJ, Dubois L, Samarska IV, Wieten L, Aarts MJB, et al. Immunotherapy as sensitizer for local radiotherapy. Oncoimmunology. 2020;9:1832760.
Ban Y, Markowitz GJ, Zou Y, Ramchandani D, Kraynak J, Sheng J, et al. Radiation-activated secretory proteins of Scgb1a1+ club cells increase the efficacy of immune checkpoint blockade in lung cancer. Nature Cancer. 2021;2:919–31.
Lan Y, Moustafa M, Knoll M, Xu C, Furkel J, Lazorchak A, et al. Simultaneous targeting of TGF-beta/PD-L1 synergizes with radiotherapy by reprogramming the tumor microenvironment to overcome immune evasion. Cancer Cell. 2021;39:1388-403e10.
Ciardiello D, Vitiello PP, Cardone C, Martini G, Troiani T, Martinelli E, et al. Immunotherapy of colorectal cancer: challenges for therapeutic efficacy. Cancer Treat Rev. 2019;76:22–32.
Bear AS, Vonderheide RH, O’Hara MH. Challenges and opportunities for pancreatic cancer immunotherapy. Cancer Cell. 2020;38:788–802.
Parikh AR, Szabolcs A, Allen JN, Clark JW, Wo JY, Raabe M, et al. Radiation therapy enhances immunotherapy response in microsatellite stable colorectal and pancreatic adenocarcinoma in a phase II trial. Nat Cancer. 2021;2:1124–35.
Theelen W, Peulen HMU, Lalezari F, van der Noort V, de Vries JF, Aerts J, et al. Effect of pembrolizumab after stereotactic body radiotherapy vs pembrolizumab alone on tumor response in patients with advanced non-small cell lung cancer: results of the PEMBRO-RT phase 2 randomized clinical trial. JAMA Oncol. 2019;5:1276–82.
Foster CC, Fleming GF, Karrison TG, Liao CY, Desai AV, Moroney JW, et al. Phase I study of stereotactic body radiotherapy plus nivolumab and urelumab or cabiralizumab in advanced solid tumors. Clin Cancer Res. 2021;27:5510–8.
Forde PM, Chaft JE, Smith KN, Anagnostou V, Cottrell TR, Hellmann MD, et al. Neoadjuvant PD-1 blockade in resectable lung cancer. N Engl J Med. 2018;378:1976–86.
Pircher A, Gamerith G, Amann A, Reinold S, Popper H, Gachter A, et al. Neoadjuvant chemo-immunotherapy modifies CD4(+)CD25(+) regulatory T cells (Treg) in non-small cell lung cancer (NSCLC) patients. Lung Cancer. 2014;85:81–7.
Yousefi H, Yuan J, Keshavarz-Fathi M, Murphy JF, Rezaei N. Immunotherapy of cancers comes of age. Expert Rev Clin Immunol. 2017;13:1001–15.
Lastwika KJ, Wilson W 3rd, Li QK, Norris J, Xu H, Ghazarian SR, et al. Control of PD-L1 expression by oncogenic activation of the AKT-mTOR pathway in non-small cell lung cancer. Cancer Res. 2016;76:227–38.
Song M, Chen D, Lu B, Wang C, Zhang J, Huang L, et al. PTEN loss increases PD-L1 protein expression and affects the correlation between PD-L1 expression and clinical parameters in colorectal cancer. PLoS ONE. 2013;8:e65821.
Jiang X, Zhou J, Giobbie-Hurder A, Wargo J, Hodi FS. The activation of MAPK in melanoma cells resistant to BRAF inhibition promotes PD-L1 expression that is reversible by MEK and PI3K inhibition. Clin Cancer Res Off J Am Assoc Cancer Res. 2013;19:598–609.
Chen N, Fang W, Zhan J, Hong S, Tang Y, Kang S, et al. Upregulation of PD-L1 by EGFR activation mediates the immune escape in EGFR-driven NSCLC: implication for optional immune targeted therapy for NSCLC patients with EGFR mutation. J Thorac Oncol. 2015;10:910–23.
Voli F, Valli E, Lerra L, Kimpton K, Saletta F, Giorgi FM, et al. Intratumoral copper modulates PD-L1 expression and influences tumor immune evasion. Cancer Res. 2020;80:4129–44.
Alsuliman A, Colak D, Al-Harazi O, Fitwi H, Tulbah A, Al-Tweigeri T, et al. Bidirectional crosstalk between PD-L1 expression and epithelial to mesenchymal transition: significance in claudin-low breast cancer cells. Mol Cancer. 2015;14:149.
Garcia-Diaz A, Shin DS, Moreno BH, Saco J, Escuin-Ordinas H, Rodriguez GA, et al. Interferon receptor signaling pathways regulating PD-L1 and PD-L2 expression. Cell Rep. 2017;19:1189–201.
Wu SY, Xiao Y, Wei JL, Xu XE, Jin X, Hu X, et al. MYC suppresses STING-dependent innate immunity by transcriptionally upregulating DNMT1 in triple-negative breast cancer. J Immunother Cancer. 2021;9:e002528.
Kwon J, Bakhoum SF. The cytosolic DNA-sensing cGAS-STING pathway in cancer. Cancer Discov. 2020;10:26–39.
Bakhoum SF, Cantley LC. The multifaceted role of chromosomal instability in cancer and its microenvironment. Cell. 2018;174:1347–60.
Mackenzie KJ, Carroll P, Martin CA, Murina O, Fluteau A, Simpson DJ, et al. cGAS surveillance of micronuclei links genome instability to innate immunity. Nature. 2017;548:461–5.
Sen T, Rodriguez BL, Chen L, Corte CMD, Morikawa N, Fujimoto J, et al. Targeting DNA damage response promotes antitumor immunity through STING-mediated T-cell activation in small cell lung cancer. Cancer Discov. 2019;9:646–61.
Dang CV. MYC on the path to cancer. Cell. 2012;149:22–35.
Jaiswal S, Jamieson CH, Pang WW, Park CY, Chao MP, Majeti R, et al. CD47 is upregulated on circulating hematopoietic stem cells and leukemia cells to avoid phagocytosis. Cell. 2009;138:271–85.
Shen J, Zhao W, Ju Z, Wang L, Peng Y, Labrie M, et al. PARPi triggers the STING-dependent immune response and enhances the therapeutic efficacy of immune checkpoint blockade independent of BRCAness. Cancer Res. 2019;79:311–9.
Spranger S, Gajewski TF, Kline J. MYC—a thorn in the side of cancer immunity. Cell Res. 2016;26:639–40.
Li P, Huang T, Zou Q, Liu D, Wang Y, Tan X, et al. FGFR2 promotes expression of PD-L1 in colorectal cancer via the JAK/STAT3 signaling pathway. J Immunol. 2019;202:3065–75.
Kearney CJ, Vervoort SJ, Hogg SJ, Ramsbottom KM, Freeman AJ, Lalaoui N, et al. Tumor immune evasion arises through loss of TNF sensitivity. Sci Immunol. 2018;3:eaar3451.
Sumimoto H, Takano A, Teramoto K, Daigo Y. RAS-mitogen-activated protein kinase signal is required for enhanced PD-L1 expression in human lung cancers. PLoS ONE. 2016;11:e0166626.
Grenda A, Nicos M, Szczyrek M, Krawczyk P, Kucharczyk T, Jarosz B, et al. MicroRNAs aid the assessment of programmed death ligand 1 expression in patients with non-small cell lung cancer. Oncol Lett. 2019;17:5193–200.
Zhang L, Yao J, Wei Y, Zhou Z, Li P, Qu J, et al. Blocking immunosuppressive neutrophils deters pY696-EZH2-driven brain metastases. Sci Transl Med. 2020;12:eaaz5387.
Zelenay S, van der Veen AG, Bottcher JP, Snelgrove KJ, Rogers N, Acton SE, et al. Cyclooxygenase-dependent tumor growth through evasion of immunity. Cell. 2015;162:1257–70.
Lu X, Horner JW, Paul E, Shang X, Troncoso P, Deng P, et al. Effective combinatorial immunotherapy for castration-resistant prostate cancer. Nature. 2017;543:728–32.
Wang Y, Liu S, Yang Z, Algazi AP, Lomeli SH, Wang Y, et al. Anti-PD-1/L1 lead-in before MAPK inhibitor combination maximizes antitumor immunity and efficacy. Cancer Cell. 2021;39:1375–87.
Qi Z, Xu Z, Zhang L, Zou Y, Li J, Yan W, et al. Overcoming resistance to immune checkpoint therapy in PTEN-null prostate cancer by intermittent anti-PI3Kalpha/beta/delta treatment. Nat Commun. 2022;13:182.
Marabelle A, Tselikas L, de Baere T, Houot R. Intratumoral immunotherapy: using the tumor as the remedy. Ann Oncol. 2017;28:xii33–43.
Karapetyan L, Luke JJ, Davar D. Toll-like receptor 9 agonists in cancer. Onco Targets Ther. 2020;13:10039–60.
Dai X, Bu X, Gao Y, Guo J, Hu J, Jiang C, et al. Energy status dictates PD-L1 protein abundance and anti-tumor immunity to enable checkpoint blockade. Mol Cell. 2021;81:2317–31.
Cha JH, Yang WH, Xia W, Wei Y, Chan LC, Lim SO, et al. Metformin promotes antitumor immunity via endoplasmic-reticulum-associated degradation of PD-L1. Mol Cell. 2018;71:606-20e7.
Li N, Wang J, Zhang N, Zhuang M, Zong Z, Zou J, et al. Cross-talk between TNF-alpha and IFN-gamma signaling in induction of B7–H1 expression in hepatocellular carcinoma cells. Cancer Immunol Immunother. 2018;67:271–83.
Hanna RM, Abdelnour L, Hasnain H, Selamet U, Kurtz I. Intravitreal bevacizumab-induced exacerbation of proteinuria in diabetic nephropathy, and amelioration by switching to ranibizumab. SAGE Open Med Case Rep. 2020;8:2050313X20907033.
Martinez-Usatorre A, Kadioglu E, Boivin G, Cianciaruso C, Guichard A, Torchia B, et al. Overcoming microenvironmental resistance to PD-1 blockade in genetically engineered lung cancer models. Sci Transl Med. 2021;13:eabd1616.
Huinen ZR, Huijbers EJM, van Beijnum JR, Nowak-Sliwinska P, Griffioen AW. Anti-angiogenic agents—overcoming tumour endothelial cell anergy and improving immunotherapy outcomes. Nat Rev Clin Oncol. 2021;18:527–40.
Li X, Li Y, Lu W, Chen M, Ye W, Zhang D. The Tumor vessel targeting strategy: a double-edged sword in tumor metastasis. Cells. 2019;8:1602.
Ma H, Yang W, Zhang L, Liu S, Zhao M, Zhou G, et al. Interferon-alpha promotes immunosuppression through IFNAR1/STAT1 signalling in head and neck squamous cell carcinoma. Br J Cancer. 2019;120:317–30.
Moghanizadeh-Ashkezari M, Shokrollahi P, Zandi M, Shokrolahi F, Daliri MJ, Kanavi MR, et al. Vitamin C loaded poly(urethane-urea)/ZnAl-LDH aligned scaffolds increase proliferation of corneal keratocytes and up-regulate vimentin secretion. ACS Appl Mater Interfaces. 2019;11:35525–39.
Fu J, Wu Z, Liu J, Wu T. Vitamin C: a stem cell promoter in cancer metastasis and immunotherapy. Biomed Pharmacother. 2020;131:110588.
Magri A, Germano G, Lorenzato A, Lamba S, Chila R, Montone M, et al. High-dose vitamin C enhances cancer immunotherapy. Sci Transl Med. 2020;12:eaay8707.
Luchtel RA, Bhagat T, Pradhan K, Jacobs WR Jr, Levine M, Verma A, et al. High-dose ascorbic acid synergizes with anti-PD1 in a lymphoma mouse model. Proc Natl Acad Sci U S A. 2020;117:1666–77.
Lam KC, Araya RE, Huang A, Chen Q, Di Modica M, Rodrigues RR, et al. Microbiota triggers STING-type I IFN-dependent monocyte reprogramming of the tumor microenvironment. Cell. 2021;184:5338-56e21.
Caffa I, Spagnolo V, Vernieri C, Valdemarin F, Becherini P, Wei M, et al. Fasting-mimicking diet and hormone therapy induce breast cancer regression. Nature. 2020;583:620–4.
Zhang H, Xia Y, Wang F, Luo M, Yang K, Liang S, et al. Aldehyde dehydrogenase 2 mediates alcohol-induced colorectal cancer immune escape through stabilizing PD-L1 expression. Adv Sci (Weinh). 2021;8:2003404.
Addeo A, Banna GL, Metro G, Di Maio M. Chemotherapy in combination with immune checkpoint inhibitors for the first-line treatment of patients with advanced non-small cell lung cancer: a systematic review and literature-based meta-analysis. Front Oncol. 2019;9:264.
Rosenberg SA, Yang JC, Sherry RM, Kammula US, Hughes MS, Phan GQ, et al. Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy. Clin Cancer Res. 2011;17:4550–7.
Tran E, Turcotte S, Gros A, Robbins PF, Lu YC, Dudley ME, et al. Cancer immunotherapy based on mutation-specific CD4+ T cells in a patient with epithelial cancer. Science. 2014;344:641–5.
Stevanovic S, Draper LM, Langhan MM, Campbell TE, Kwong ML, Wunderlich JR, et al. Complete regression of metastatic cervical cancer after treatment with human papillomavirus-targeted tumor-infiltrating T cells. J Clin Oncol. 2015;33:1543–50.
Tran E, Robbins PF, Lu YC, Prickett TD, Gartner JJ, Jia L, et al. T-cell transfer therapy targeting mutant KRAS in cancer. N Engl J Med. 2016;375:2255–62.
Zacharakis N, Chinnasamy H, Black M, Xu H, Lu YC, Zheng Z, et al. Immune recognition of somatic mutations leading to complete durable regression in metastatic breast cancer. Nat Med. 2018;24:724–30.
Creelan BC, Wang C, Teer JK, Toloza EM, Yao J, Kim S, et al. Tumor-infiltrating lymphocyte treatment for anti-PD-1-resistant metastatic lung cancer: a phase 1 trial. Nat Med. 2021;27:1410–8.
Gargett T, Yu W, Dotti G, Yvon ES, Christo SN, Hayball JD, et al. GD2-specific CAR T cells undergo potent activation and deletion following antigen encounter but can be protected from activation-induced cell death by PD-1 blockade. Mol Ther. 2016;24:1135–49.
Rafiq S, Yeku OO, Jackson HJ, Purdon TJ, van Leeuwen DG, Drakes DJ, et al. Targeted delivery of a PD-1-blocking scFv by CAR-T cells enhances anti-tumor efficacy in vivo. Nat Biotechnol. 2018;36:847–56.
Chon HJ, Lee WS, Yang H, Kong SJ, Lee NK, Moon ES, et al. Tumor microenvironment remodeling by intratumoral oncolytic vaccinia virus enhances the efficacy of immune-checkpoint blockade. Clin Cancer Res. 2019;25:1612–23.
Kaufman HL, Kohlhapp FJ, Zloza A. Oncolytic viruses: a new class of immunotherapy drugs. Nat Rev Drug Discov. 2015;14:642–62.
Zuo S, Wei M, Xu T, Kong L, He B, Wang S, et al. An engineered oncolytic vaccinia virus encoding a single-chain variable fragment against TIGIT induces effective antitumor immunity and synergizes with PD-1 or LAG-3 blockade. J Immunother Cancer. 2021;9:e002843.
Shi G, Yang Q, Zhang Y, Jiang Q, Lin Y, Yang S, et al. Modulating the tumor microenvironment via oncolytic viruses and CSF-1R inhibition synergistically enhances anti-PD-1 immunotherapy. Mol Ther. 2019;27:244–60.
Lei K, Kurum A, Kaynak M, Bonati L, Han Y, Cencen V, et al. Cancer-cell stiffening via cholesterol depletion enhances adoptive T-cell immunotherapy. Nat Biomed Eng. 2021;5:1411–25.
Kjeldsen JW, Lorentzen CL, Martinenaite E, Ellebaek E, Donia M, Holmstroem RB, et al. A phase 1/2 trial of an immune-modulatory vaccine against IDO/PD-L1 in combination with nivolumab in metastatic melanoma. Nat Med. 2021;27:2212–23.
Qian DC, Kleber T, Brammer B, Xu KM, Switchenko JM, Janopaul-Naylor JR, et al. Effect of immunotherapy time-of-day infusion on overall survival among patients with advanced melanoma in the USA (MEMOIR): a propensity score-matched analysis of a single-centre, longitudinal study. Lancet Oncol. 2021;22:1777–86.
Long JE, Drayson MT, Taylor AE, Toellner KM, Lord JM, Phillips AC. Morning vaccination enhances antibody response over afternoon vaccination: a cluster-randomised trial. Vaccine. 2016;34:2679–85.
Re GL, Santeufemia DA, Re FL, Bortolus R, Doretto P, Marus W, et al. Interleukin-2 chronotherapy for metastatic renal cell carcinoma: results of a phase I-II study. Cytokine. 2020;128:154984.
Chabanon RM, Rouanne M, Lord CJ, Soria JC, Pasero P, Postel-Vinay S. Targeting the DNA damage response in immuno-oncology: developments and opportunities. Nat Rev Cancer. 2021;21:701–17.
Li H, Xiao Y, Li Q, Yao J, Yuan X, Zhang Y, et al. The allergy mediator histamine confers resistance to immunotherapy in cancer patients via activation of the macrophage histamine receptor H1. Cancer Cell. 2022;40:36-52.e9.
Wang N, Liu C, Lu Z, Yang W, Li L, Gong S, et al. Multistage sensitive nanoCRISPR enable efficient intracellular disruption of immune checkpoints for robust innate and adaptive immune coactivation. Adv Funct Mat. 2020;30:2004940.
Panagioti E, Kurokawa C, Viker K, Ammayappan A, Anderson SK, Sotiriou S, et al. Immunostimulatory bacterial antigen-armed oncolytic measles virotherapy significantly increases the potency of anti-PD1 checkpoint therapy. J Clin Investig. 2021;131:141614.
Lim SO, Li CW, Xia W, Cha JH, Chan LC, Wu Y, et al. Deubiquitination and stabilization of PD-L1 by CSN5. Cancer Cell. 2016;30:925–39.
Rawangkan A, Wongsirisin P, Namiki K, Iida K, Kobayashi Y, Shimizu Y, et al. Green tea catechin is an alternative immune checkpoint inhibitor that inhibits PD-L1 expression and lung tumor growth. Molecules. 2018;23:2071.
Koikawa K, Kibe S, Suizu F, Sekino N, Kim N, Manz TD, et al. Targeting Pin1 renders pancreatic cancer eradicable by synergizing with immunochemotherapy. Cell. 2021;184:4753-71e27.
Qiu X, Yang S, Wang S, Wu J, Zheng B, Wang K, et al. M(6)A demethylase ALKBH5 regulates PD-L1 expression and tumor immunoenvironment in intrahepatic cholangiocarcinoma. Cancer Res. 2021;81:4778–93.
Li CW, Lim SO, Chung EM, Kim YS, Park AH, Yao J, et al. Eradication of triple-negative breast cancer cells by targeting glycosylated PD-L1. Cancer Cell. 2018;33:187-201e10.
Jin S, Muhammad N, Sun Y, Tan Y, Yuan H, Song D, et al. Multispecific platinum(IV) complex deters breast cancer via interposing inflammation and immunosuppression as an inhibitor of COX-2 and PD-L1. Angew Chem Int Ed Engl. 2020;59:23313–21.
Guo L, Li H, Fan T, Ma Y, Wang L. Synergistic efficacy of curcumin and anti-programmed cell death-1 in hepatocellular carcinoma. Life Sci. 2021;279:119359.
Wang Y, Yu J, Luo Z, Shi Q, Liu G, Wu F, et al. Engineering endogenous tumor-associated macrophage-targeted biomimetic nano-RBC to reprogram tumor immunosuppressive microenvironment for enhanced chemo-immunotherapy. Adv Mater. 2021;33:e2103497.
Li H, Kuang X, Liang L, Ye Y, Zhang Y, Li J, et al. The beneficial role of sunitinib in tumor immune surveillance by regulating tumor PD-L1. Adv Sci (Weinh). 2021;8:2001596.
Shajib MS, Khan WI. The role of serotonin and its receptors in activation of immune responses and inflammation. Acta Physiol (Oxf). 2015;213:561–74.
Sarrouilhe D, Mesnil M. Serotonin and human cancer: a critical view. Biochimie. 2019;161:46–50.
Geuijen C, Tacken P, Wang LC, Klooster R, van Loo PF, Zhou J, et al. A human CD137xPD-L1 bispecific antibody promotes anti-tumor immunity via context-dependent T cell costimulation and checkpoint blockade. Nat Commun. 2021;12:4445.
Tanoue K, Rosewell Shaw A, Watanabe N, Porter C, Rana B, Gottschalk S, et al. Armed oncolytic adenovirus-expressing PD-L1 mini-body enhances antitumor effects of chimeric antigen receptor T cells in solid tumors. Cancer Res. 2017;77:2040–51.
Jiang H, Ni H, Zhang P, Guo X, Wu M, Shen H, et al. PD-L1/LAG-3 bispecific antibody enhances tumor-specific immunity. Oncoimmunology. 2021;10:1943180.
Heim L, Friedrich J, Engelhardt M, Trufa DI, Geppert CI, Rieker RJ, et al. NFATc1 promotes antitumoral effector functions and memory CD8(+) T-cell differentiation during non-small cell lung cancer development. Cancer Res. 2018;78:3619–33.
Zhang Y, Zeng Y, Liu T, Du W, Zhu J, Liu Z, et al. The canonical TGF-beta/Smad signalling pathway is involved in PD-L1-induced primary resistance to EGFR-TKIs in EGFR-mutant non-small-cell lung cancer. Respir Res. 2019;20:164.
Krueger J, Santinon F, Kazanova A, Issa ME, Larrivee B, Kremer R, et al. Hydroxychloroquine (HCQ) decreases the benefit of anti-PD-1 immune checkpoint blockade in tumor immunotherapy. PLoS ONE. 2021;16:e0251731.
Simian M, Bissell MJ. Organoids: a historical perspective of thinking in three dimensions. J Cell Biol. 2017;216:31–40.
Verduin M, Hoeben A, De Ruysscher D, Vooijs M. Patient-derived cancer organoids as predictors of treatment response. Front Oncol. 2021;11:641980.
Chakrabarti J, Koh V, Steele N, Hawkins J, Ito Y, Merchant JL, et al. Disruption of Her2-induced PD-L1 inhibits tumor cell immune evasion in patient-derived gastric cancer organoids. Cancers (Basel). 2021;13:6158.
Koh V, Chakrabarti J, Torvund M, Steele N, Hawkins JA, Ito Y, et al. Hedgehog transcriptional effector GLI mediates mTOR-induced PD-L1 expression in gastric cancer organoids. Cancer Lett. 2021;518:59–71.
Holokai L, Chakrabarti J, Lundy J, Croagh D, Adhikary P, Richards SS, et al. Murine- and human-derived autologous organoid/immune cell co-cultures as pre-clinical models of pancreatic ductal adenocarcinoma. Cancers (Basel). 2020;12:3816.