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Table 4 Nanomaterials applied in cancer immunotherapy

From: Nanomaterials for cancer therapy: current progress and perspectives

Name of drug

Component

Cancer types tested

Outcome

References

G7-aPD-L1

Dendrimer and anti-PD-L1 antibody

Human renal carcinoma and breast cancer cells

G7-aPD-L1 showed significantly enhanced binding strength to PD-L1 proteins compared to free aPD-L1

[218]

Doxil synergized with mAbs

Liposomal doxorubicin, anti-PD-1 and CTLA-4 mAbs

Mouse colon cancer cells and mouse fibrosarcoma cells

Doxil synergized with anti-PD-1 and CTLA-4 mAbs in a preventative CT26 mouse tumor model and Doxil activity increased in the presence of a functional immune system

[220]

NPsiCTLA-4

Nanoparticle, CTLA-4 siRNA

B16 melanoma mouse model

NPsiCTLA-4 delivered CTLA-4-siRNA into tumor sites and affected T cell subsets, exhibiting augmented T cell activation. Induced anti-tumor immune responses

[221]

NP-based mRNA vaccine

Nanoparticle, mRNA encoding tumor antigen Mucin-1

Mouse triple negative breast cancer cells and female BALB/c mice

The NP-based mRNA vaccine successfully expressed tumor antigen in mouse lymph node and a synergic anti-tumor effect was shown

[222]

rGO/MTX/SB

rGO, MTX, transforming growth factor beta inhibitor SB-431542 (SB)

Triple negative breast cancer mouse model

A synergistic chemo-immuno-photothermal anti-tumor effect by in situ vaccination and TME inhibition was exhibited after laser irradiation

[223]

IFN-γNE2

Nanoemulsion, IFN-γ

Human breast cancer cells

IFN-γNE2 reduced MCF-7 cell viability without affecting phagocytes and induced cellular activity of phagocytes

[107]

  1. CTLA-4, Cytotoxic T-lymphocyte-associated protein 4; mAbs, Monoclonal antibodies; MTX, Methotrexate; IFN-γ, Cytokine Interferon gamma; NE, Nanoemulsions; PD-L1, Programmed cell death ligand 1; rGO, Reduced graphene oxide