The effects of β-glucan on human immune and cancer cells
Journal of Hematology & Oncology volume 2, Article number: 25 (2009)
Non-prescriptional use of medicinal herbs among cancer patients is common around the world. The alleged anti-cancer effects of most herbal extracts are mainly based on studies derived from in vitro or in vivo animal experiments. The current information suggests that these herbal extracts exert their biological effect either through cytotoxic or immunomodulatory mechanisms. One of the active compounds responsible for the immune effects of herbal products is in the form of complex polysaccharides known as β-glucans. β-glucans are ubiquitously found in both bacterial or fungal cell walls and have been implicated in the initiation of anti-microbial immune response. Based on in vitro studies, β-glucans act on several immune receptors including Dectin-1, complement receptor (CR3) and TLR-2/6 and trigger a group of immune cells including macrophages, neutrophils, monocytes, natural killer cells and dendritic cells. As a consequence, both innate and adaptive response can be modulated by β-glucans and they can also enhance opsonic and non-opsonic phagocytosis. In animal studies, after oral administration, the specific backbone 1→3 linear β-glycosidic chain of β-glucans cannot be digested. Most β-glucans enter the proximal small intestine and some are captured by the macrophages. They are internalized and fragmented within the cells, then transported by the macrophages to the marrow and endothelial reticular system. The small β-glucans fragments are eventually released by the macrophages and taken up by other immune cells leading to various immune responses. However, β-glucans of different sizes and branching patterns may have significantly variable immune potency. Careful selection of appropriate β-glucans is essential if we wish to investigate the effects of β-glucans clinically. So far, no good quality clinical trial data is available on assessing the effectiveness of purified β-glucans among cancer patients. Future effort should direct at performing well-designed clinical trials to verify the actual clinical efficacy of β-glucans or β-glucans containing compounds.
A significant proportion of cancer patients have been taking complementary medical therapies while receiving their conventional anti-cancer treatments [1–6]. Among them, herbal extracts such as Ganoderma lucidum are one of the most common modalities being consumed especially among Oriental [7–10]. Two mechanisms have been proposed to be responsible for the anti-cancer action of these herbal extracts; one is via direct cytotoxic effect and the other is indirectly through immunomodulatory action [11, 12]. Many cytotoxic chemotherapeutic agents currently in use such as vincristine, taxol and etoposide are originally purified from herbs. On the other hand, herbs with immunomodulatory functions have mainly been advocated by commercial sectors and most of them can be directly purchased over the counter or the internet. Unfortunately, organized efforts to investigate the actual usefulness of this group of herbs as well as their active ingredients are lacking. In recent years, one of the active ingredients responsible for the immunomodulation of many of these herbs was found to be a form of complex polysaccharides known as "β-D-glucan", or simply called β-glucan [8, 13]. The receptors and mechanisms of action of β-glucans have recently been unfolded via in vitro and in vivo animal experiments. Since β-glucans are inexpensive and have good margin of safety based on historical track records, their potential therapeutic value deserve further investigation. We reviewed here the literature and our experience on the in vitro and in vivo animal biological studies of β-glucans, particularly on their immune and anti-cancer mechanisms.
Physical and chemical properties of β-glucan
β-glucans are one of the most abundant forms of polysaccharides found inside the cell wall of bacteria and fungus. All β-glucans are glucose polymers linked together by a 1→ 3 linear β-glycosidic chain core and they differ from each other by their length and branching structures  (Figure 1). The branches derived from the glycosidic chain core are highly variable and the 2 main groups of branching are 1→4 or 1→6 glycosidic chains. These branching assignments appear to be species specific, for example, β-glucans of fungus have 1→6 side branches whereas those of bacteria have 1→4 side branches. The alignments of branching follow a particular ratio and branches can arise from branches (secondary branches). In aqueous solution, β-glucans undergo conformational change into triple helix, single helix or random coils. The immune functions of β-glucans are apparently dependent on their conformational complexity . It has been suggested that higher degree of structural complexity is associated with more potent immunmodulatory and anti-cancer effects.
For research purposes, the composition or structural information of β-glucans can be evaluated by a variety of methods including liquid chromatography/mass spectrometry (LC/MS), high performance liquid chromatography (HPLC) and less often X-ray crystallography  or atomic force microscopy . However, due to the tedious and lack of quantitative nature of most of these technical methods, they cannot be applied routinely as a screening tool. Other less sophisticated techniques in studying the β-glucans contents include phenol-sulphuric acid carbohydrate assay, aniline blue staining method and ELISA. Because chemical modification invariably induces changes in the natural conformation, most of these methods cannot reflect the genuine relationship between the structure and the bioactivity. Among them, aniline blue staining method is a relatively simple method to screen for β-glucan because of its ability to retain the natural conformation of β-glucans during the staining process. It also has a good specificity for β-glucans but its limitation is that it can only measure the core 1→3 linear glycosidic chain and not the branches.
Endotoxin contamination is another important issue affecting the safety and potential biological effect of β-glucan. Lipopolysaccharide (LPS) is an endotoxin found inside the Gram negative bacterial cell wall and consists of three main parts including lipid A, core and polysaccharide chain . Among them, lipid A was found to be the major component that can initiate an immune response. LPS contamination can occur during the culture or preparation of β-glucans. Since LPS is one of the most potent immune stimulator and its contamination can lead to false positive results in immune tests, quantification of LPS should be performed, which can be evaluated by either the rabbit pyrogen test or the modified limulus amebocyte lysate (LAL) assay with devoid factor G .
Pharmacodynamics & Pharmacokinetics of β-glucan
Most β-glucans are considered as non-digestible carbohydrates and are fermented to various degrees by the intestinal microbial flora [22–24]. Therefore, it has been speculated that their immunomodulatory properties may be partly attributed to a microbial dependent effect. However, β-glucans in fact can directly bind to specific receptors of immune cells, suggesting a microbial independent immunomodulatory effect . The pharmacodynamics and pharmacokinetics of β-glucans have been studied in animal and human models.
Study using a suckling rat model for evaluation of the absorption and tissues distribution of enterally administered radioactive labeled β-glucan, it was found that the majority of β-glucan was detected in the stomach and duodenum 5 minutes after the administration . This amount rapidly decreased during first 30 minutes. A significant amount of β-glucan entered the proximal intestine shortly after ingestion. Its transit through the proximal intestine decreased with time with a simultaneous increase in the ileum. Despite low systemic blood levels (less than 0.5%), significant systemic immunomodulating effects in terms of humoral and cellular immune responses were demonstrated.
The pharmacokinetics following intravenous administration of 3 different highly purified and previously characterized β-glucans were studied using carbohydrates covalently labeled with a fluorophore on the reducing terminus. The variations in molecular size, branching frequency and solution conformation were shown to have an impact on the elimination half-life, volume of distribution and clearance .
The low systemic blood level of β-glucans after ingestion does not reflect the full picture of the pharmacodynamics of β-glucans and does not rule out its in vivo effects. Cheung-VKN et al. labeled β-glucans with fluorescein to track their oral uptake and processing in vivo. The orally administered β-glucans were taken up by macrophages via the Dectin-1 receptor and was subsequently transported to the spleen, lymph nodes, and bone marrow. Within the bone marrow, the macrophages degraded the large β-1,3-glucans into smaller soluble β-1,3-glucan fragments. These fragments were subsequently taken up via the complement receptor 3 (CR3) of marginated granulocytes. These granulocytes with CR3-bound β-glucan-fluorescein were shown to kill inactivated complement 3b (iC3b)-opsonized tumor cells after they were recruited to a site of complement activation such as tumor cells coated with monoclonal antibody  (Figure 2). It was also shown that intravenous administered soluble β-glucans can be delivered directly to the CR3 on circulating granulocytes.
Furthermore, Rice PJ et al. showed that soluble β-glucans such as laminarin and scleroglucan can be directly bound and internalized by intestinal epithelial cells and gut associated lymphoid tissue (GALT) cells . Unlike macrophage, the internalization of soluble β-glucan by intestinal epithelial cells is not Dectin-1 dependent. However, the Dectin-1 and TLR-2 are accountable for uptake of soluble β-glucan by GALT cells. Another significant finding of this study is that the absorbed β-glucans can increase the resistance of mice to bacterial infection challenge.
How β-glucans mediate their effects after ingestion in human remained to be defined. In a phase I study for the assessment of safety and tolerability of a soluble form oral β-glucans . β-glucans of different doses (100 mg/day, 200 mg/day or 400 mg/day) were given respectively for 4 consecutive days. No drug-related adverse events were observed. Repeated measurements of β-glucans in serum, however, revealed no systemic absorption of the agent following the oral administration. Nonetheless, the immunoglobulin A concentration in saliva increased significantly for the 400 mg/day arm, suggesting a systemic immune effect has been elicited. One limitation of this study is the low sensitivity of serum β-glucans determination.
In summary, based on mostly animal data, β-glucans enter the proximal small intestine rapidly and are captured by the macrophages after oral administration. The β-glucans are then internalized and fragmented into smaller sized β-glucans and are carried to the marrow and endothelial reticular system. The small β-glucans fragments are then released by the macrophages and taken up by the circulating granulocytes, monocytes and dendritic cells. The immune response will then be elicited. However, we should interpret this information with caution as most of the proposed mechanisms are based on in vitro and in vivo animal studies. Indeed, there is little to no evidence for these hypothesized mechanisms of action and pharmacokinetics occurred in human subjects at the moment.
β-glucans as immunomodulating agent
Current data suggests that β-glucans are potent immunomodulators with effects on both innate and adaptive immunity. The ability of the innate immune system to quickly recognize and respond to an invading pathogen is essential for controlling infection. Dectin-1, which is a type II transmembrane protein receptor that binds β-1,3 and β-1,6 glucans, can initiate and regulate the innate immune response [31–33]. It recognizes β-glucans found in the bacterial or fungal cell wall with the advantage that β-glucans are absent in human cells. It then triggers effective immune responses including phagocytosis and proinflammatory factors production, leading to the elimination of infectious agents [34, 35]. Dectin-1 is expressed on cells responsible for innate immune response and has been found in macrophages, neutrophils, and dendritic cells . The Dectin-1 cytoplasmic tail contains an immunoreceptor tyrosine based activation motif (ITAM) that signals through the tyrosine kinase in collaboration with Toll-like receptors 2 and 6 (TLR-2/6) [34, 37, 38]. The entire signaling pathway downstream to dectin-1 activation has not yet been fully mapped out but several signaling molecules have been reported to be involved. They are NF-κB (through Syk-mediate pathway), signaling adaptor protein CARD9 and nuclear factor of activated T cells (NFAT) [39–41] (Fig. 3). This will eventually lead to the release of cytokines including interleukin (IL)-12, IL-6, tumor necrosis factor (TNF)-α, and IL-10. Some of these cytokines may play important role in the cancer therapy. On the other hand, the dendritic cell-specific ICAM-3-grabbing non-integrin homolog, SIGN-related 1 (SIGNR1) is another major mannose receptor on macrophages that cooperates with the Dectin-1 in non-opsonic recognition of β-glucans for phagocytosis  (Fig 3). Furthermore, it was found that blocking of TLR-4 can inhibit the production of IL-12 p40 and IL-10 induced by purified Ganoderma glucans (PS-G), suggesting a vital role of TLR-4 signaling in glucan induced dendritic cells maturation. Such effect is also operated via the augmentation of the IκB kinase, NF-κB activity and MAPK phosphorylation . One additional point to note is that those studies implied the interaction between β-glucans and TLR all used non-purified β-glucans, therefore the actual involvement of pure β-glucans and TLR remains to be proven.
Other possible receptors and signaling pathways induced by β-glucans are less definite at the moment. For example, lentinan, a form of mushroom derived β-glucans, has been found to bind to scavenger receptor found on the surface of myeloid cells and triggers phosphatidylinositol-3 kinase (PI3K), Akt kinase and p38 mitogen-activated protein kinase (MAPK) signaling pathway (Fig. 3). But no specific β-glucans scavenger receptor has been identified so far. Candida albicans derived β-glucans but not other forms of pathogenic fungal β-glucans can bind to LacCer receptor and activate the PI-3K pathway in controlling the neutrophil migration  (Fig. 3), but such activation pathway may involve other molecules found in the Candida derived β-glucans.
We found that β-glucans can induce human peripheral blood mononuclear cells proliferation . It can also enhance phenotypic and functional maturation of monocyte derived dendritic cells with significant IL-12 and IL-10 production. Similar findings were found by Lin et al. using PS-G, in addition, treatment of dendritic cells with PS-G resulted in enhanced T cell-stimulatory capacity and increased T cell secretion of interferon-γ and IL-10 [43, 47]. This action is at least mediated in part through the Dectin-1 receptor. The potency of such immunomodulating effects differs among β-glucans and purified polysaccharides of different size and branching complexity. In general, bigger size and more complex β-glucans such as those derived from Ganoderma lucidum have higher immunomodulating potency.
The adaptive immune system functions through the combined action of antigen-presenting cells and T cells. Specifically, class I major histocompatibility complex (MHC-I) antigen presentation to CD8(+) cytotoxic T cells is limited to proteosome-generated peptides from intracellular pathogens. On the other hand, the class II MHC (MHC-II) endocytic pathway presents only proteolytic peptides from extracellular pathogens to CD4(+) T helper cells. Carbohydrates have been previously thought to stimulate immune responses independently of T cells . However, zwitterionic polysaccharides (polysaccharides that carry both positive and negative charges) such as β-glucans can activate CD4(+) T cells through the MHC-II endocytic pathway . β-glucans are processed to low molecular weight carbohydrates by a nitric oxide-mediated mechanism. These carbohydrates will then bind to MHC-II inside antigen-presenting cells such as dendritic cells for presentation to T helper cells. Initial data suggested that it subsequently leads to Th-1 response, but there are conflicting data related to this aspect. In our in vitro data, β-glucans do not tend to polarize T cells into either Th-1, Th-2 or regulatory T cells . However, recent publications suggested β-glucans such as zymosan may induce T-cells into T-reg cells in a NOD mice model . Therefore, whether β-glucans can induce important immunologic responses through T cell activation remain to be further investigated.
Another mechanism of β-glucan action is mediated via the activated complement receptor 3 (CR3, also known as CD11b/CD18), which is found on natural killer (NK) cells, neutrophils, and lymphocytes. This pathway is responsible for opsonic recognition of β-glucans leading to phagocytosis and reactor cells lysis. β-glucans bind to the lectin domain of CR3 and prime it for binding to inactivated complement 3b (iC3b) on the surface of reactor cells. The reactor cells can be of any cell type including cancer cells tagged with monoclonal antibody and coated with iC3b. The β-glucans-activated circulating cells such as the CR3 containing neutrophils will then trigger cell lysis on iC3b-coated tumor cells . Similarly, majority of the human NK cells express CR3 and it was shown that opsonization of NK cells coated with iC3b leads to an increase in the lysis of the target. The beta chain of the CR3 molecule (CD18) rather than the alpha chain (CD11b) is responsible to the β-glucan binding [51, 52].
This concept was supported by in vivo study demonstrating barley β-1,3;1,4-glucan given orally can potentiate the activity of an antitumor monoclonal antibody (anti-ganglioside-2 or "3F8"), leading to enhanced tumor regression and survival on a human neuroblastoma xenografts mouse model . 3F8 plus β-glucan was shown to produce near-complete tumor regression or disease stabilization whereas 3F8 or β-glucan alone showed no significant effect. The median survival of the 3F8 plus β-glucan group was 5.5-fold higher than that of the control groups, and up to 47% of the mice remained progression free in contrast to <3% of controls at the end of the study period. No toxicities were noted in all mice treated with β-glucan, 3F8, or 3F8 plus β-glucan.
A similar xenograft model was adopted subsequently for investigating various targeted tumor antigens and tumor types. It was found that β-glucan exerts similar anti-tumor effects irrespective of antigens (GD2, GD3, CD20, epidermal growth factor-receptor, and HER-2) or human tumor types (neuroblastoma, melanoma, lymphoma, epidermoid carcinoma, and breast carcinoma) or tumor sites (subcutaneous versus systemic). The effect was correlated with the molecular size of the β-1,3;1,4-glucan [53, 54].
Furthermore, 2 other receptors known as scavenger  and lactosylceramide [56, 57] also bind β-glucans and can elicit a range of responses. β-glucans can enhance endotoxin clearance via scavenger receptors by decreasing TNF production leading to improved survival in rats subjected to Escherichia coli sepsis . On the other hand, β-glucans binding to lactosylceramide receptor can enhance myeloid progenitor proliferation and neutrophil oxidative burst response, leading to an increase in leukocyte anti-microbial activity. It is also associated with the activation of NF-κB in human neutrophils . Again in other studies, structurally different β-glucans appear to have different affinity toward these receptors. For example, only high molecular weight β-glucans can effectively bind to the lactosylceramide receptor. Therefore, markedly different host responses induced by different β-glucans are expected.
In summary, β-glucans act on a diversity of immune related receptors in particularly Dectin-1 and CR3, and can trigger a wide spectrum of immune responses. The targeted immune cells of β-glucans include macrophages, neutrophils, monocytes, NK cells and dendritic cells (Figure 3). The immunomodulatory functions induced by β-glucans involve both innate and adaptive immune response. β-glucans also enhance opsonic and non-opsonic phagocytosis. Whether β-glucans polarize the T cells subset towards a particular direction remains to be explored.
Anti-cancer effects of β-glucans
It is becoming clear that β-glucans themselves have no direct cytotoxic effects. Studies implicating the cytotoxic effects of β-glucans were either from studies using crude extracts of β-glucan containing herbs or the use of β-glucan primed monocytes. For β-glucan containing herbs like Ganoderma lucidum (Lingzhi), there are other active components such as ganoderic acid from its mycelium  and triterpenes from its spore [61–63], which have all been shown to have direct anti-cancer effects independently. We did not find any direct cytotoxic effects of β-glucans on a panel of common cancer cell lines tested including carcinoma, sarcoma, and blastoma. β-glucans also did not trigger any apoptotic pathways and had no direct effect on the telomerase and telomeric length of the cancer cells (unpublished data). In contrast, it stimulated the proliferation of monocytic lineage leukemic cells in-vitro and can facilitate the maturation of dendritic cells derived from leukaemic cells . Hence, whether it is beneficial to apply β-glucans on leukemic patients remains controversial and has to be considered with caution.
In the English literature, there are no clinical trials that directly assessed the anti-cancer effects of purified β-glucans in cancer patients. Most studies were assessing the toxicity profile or underlying immune changes of the cancer patients without addressing on the change of cancer status. In addition, most of the related studies used either crude herbal extracts or a fraction of the extracts instead of purified β-glucans. Therefore, it is difficult to identify whether the actual effects were related to β-glucans or other confounding chemicals found in the mixture.
In a prospective clinical trial of short term immune effects of oral β-glucan in patients with advanced breast cancer, 23 female patients with advanced breast cancer were compared with 16 healthy females control . Oral β-1,3;1,6-glucan was taken daily. Blood samples were recollected on the day 0 and 15. It was found that despite a relatively low initial white cell count, oral β-glucan can stimulate proliferation and activation of peripheral blood monocytes in patients with advanced breast cancer. Whether that can be translated into clinical benefit remains unanswered.
Clinical trials on anti-cancer effects of natural products with β-glucan
Many edible fungi particularly in the mushroom species yield immunogenic substances with potential anticancer activity . β-glucans are one of the common active components (Table 1). In limited clinical trials on human cancers, most were well tolerated. Among them, lentinan derived from Lentinus edodes is a form of β-glucans . Since it has poor enteric absorption, intrapleural, intra-peritoneal  or intravenous routes had been adopted in clinical trials which showed some clinical benefit when used as an adjuvant to chemotherapy . Schizophyllan (SPG) or sizofiran is another β-glucan derived from Schizophyllan commune. Its triple helical complex β-glucans structure prevents it from adequate oral absorption so an intratumoral route or injection to regional lymph nodes had been adopted [70, 71]. In a randomized trial, SPG combined with conventional chemotherapy improved the long term survival rate of patients with ovarian cancer . But whether the prolonged survival can subsequently led to a better cure rate remain unanswered.
Maitake D-Fraction extracted from Grifola frondosa (Maitake mushroom) was found to decrease the size of the lung, liver and breast tumors in >60% of patients when it was combined with chemotherapy in a 2 arms control study comparing with chemotherapy alone . The effects were less obvious with leukemia, stomach and brain cancer patients . But the validity of the clinical study was subsequently questioned by another independent observer . Two proteoglycans from Coriolus versicolor (Yun Zhi) – PSK (Polysaccharide-K) and PSP (Polysaccharopeptide) – are among the most extensively studied β-glucan containing herbs with clinical trials information. However, both PSK and PSP are protein-bound polysaccharides, so their actions are not necessary directly equivalent to pure β-glucans . In a series of trials from Japan and China, PSK and PSP were well tolerated without significant side effects [66, 77–81]. They also prolonged the survival of some patients with carcinoma and non-lymphoid leukemia.
Ganoderma polysaccharides are β-glucans derived from Ganoderma lucidum (Lingzhi, Reishi). While β-glucan is the major component of the Ganoderma mycelium, it is only a minor component in the Ganoderma spore . The main active ingredient in the Ganoderma spore extract is triterpenoid which is cytotoxic in nature. In an open-label study on patients with advanced lung cancer, thirty-six patients were treated with 5.4 g/day Ganoderma polysaccharides for 12 weeks with inconclusive variable and results on the cytokines profiles . Another study on 47 patients with advanced colorectal cancer using the same dosage and period again demonstrated similar variable immune response patterns . These results highlight the inconsistency of clinical outcomes in using immune enhancing herbal extracts clinically, which may partly be due to the impurity of the products used.
The intrinsic differences of the β-glucans derived from different sources will elicit variable immune and anti-cancer responses. We summarized the current limitations of β-glucan research from the literature (Table 2). The limitations are further complicated by the fact that many studies on β-glucan related herbs often used crude extracts rather than purified compounds, therefore the confounding effects of other chemicals cannot be totally ruled out . Careful selection of appropriate β-glucan products with good pre-test quality control is essential if we want to understand and compare the results on how β-glucans act on our immune system and exerting anti-cancer effects. A possibly well-defined β-glucan standard is urgently needed in this field for controlled experiments. So far, there are very few clinical trial data on using purified β-glucans for cancer patients. Future studies should aim to obtain such information so it can assist us in applying β-glucans rationally and effectively to our cancer patients in the future.
Kim MJ, Lee SD, Kim DR, Kong YH, Sohn WS, Ki SS, Kim J, Kim YC, Han CJ, Lee JO: Use of complementary and alternative medicine among Korean cancer patients. The Korean journal of internal medicine. 2004, 19 (4): 250-256.
McEachrane-Gross FP, Liebschutz JM, Berlowitz D: Use of selected complementary and alternative medicine (CAM) treatments in veterans with cancer or chronic pain: a cross-sectional survey. BMC complementary and alternative medicine. 2006, 6: 34-10.1186/1472-6882-6-34.
Inglin S, Amsler S, Arigoni F, Burton-Jeangros C, Pargoux-Vallade C, Sappino AP: [Complementary medicine use in oncology patients]. Revue medicale suisse. 2008, 4 (158): 1264-1266.
Armstrong TS, Gilbert MR: Use of complementary and alternative medical therapy by patients with primary brain tumors. Current neurology and neuroscience reports. 2008, 8 (3): 264-268. 10.1007/s11910-008-0040-z.
Mueller CM, Mai PL, Bucher J, Peters JA, Loud JT, Greene MH: Complementary and alternative medicine use among women at increased genetic risk of breast and ovarian cancer. BMC complementary and alternative medicine. 2008, 8: 17-10.1186/1472-6882-8-17.
Yang C, Chien LY, Tai CJ: Use of complementary and alternative medicine among patients with cancer receiving outpatient chemotherapy in Taiwan. J Altern Complement Med. 2008, 14 (4): 413-416. 10.1089/acm.2007.7181.
Chan WK, Lam DT, Law HK, Wong WT, Koo MW, Lau AS, Lau YL, Chan GC: Ganoderma lucidum mycelium and spore extracts as natural adjuvants for immunotherapy. J Altern Complement Med. 2005, 11 (6): 1047-1057. 10.1089/acm.2005.11.1047.
Chang R: Bioactive polysaccharides from traditional Chinese medicine herbs as anticancer adjuvants. J Altern Complement Med. 2002, 8 (5): 559-565. 10.1089/107555302320825066.
Chang S, Miles P: Ganoderma lucidum – a leader of medicinal mushrooms. Mushrooms: cultivation, nutritional value, medicinal effect, and environmental impact. 2004, CRC Press, 357-373. 1
Chan G, Mullen P, Ha S, Wong G, Lee T, YL L: Use of alternative medical treatments in paediatric oncology patients in Hong Kong. Annual Scientific Meeting of the Paediactric Society of Hong Kong. 1998
Wasser SP: Medicinal mushrooms as a source of antitumor and immunomodulating polysaccharides. Appl Microbiol Biotechnol. 2002, 60 (3): 258-274. 10.1007/s00253-002-1076-7.
Borchers AT, Keen CL, Gershwin ME: Mushrooms, tumors, and immunity: an update. Exp Biol Med (Maywood). 2004, 229 (5): 393-406.
Ooi VE, Liu F: Immunomodulation and anti-cancer activity of polysaccharide-protein complexes. Curr Med Chem. 2000, 7 (7): 715-729.
Stone BA, Clarke AE: Chemistry and biology of (1,3)-D-glucans. 1992, Victoria, Australia.: La Trobe University Press
Bohn J, BeMiller J: (1->3)-β-Glucans as biological response modifiers: a review of structure-functional activity relationships. Carbohydrate Polymers. 1995, 28 (1): 3-14. 10.1016/0144-8617(95)00076-3.
Hanada N, Katayama T, Kunimori A, Yamashita Y, Takehara T: Four different types of glucans synthesised by glucosyltransferases from Streptococcus sobrinus. Microbios. 1993, 73 (294): 23-35.
Rolin DB, Pfeffer PE, Osman SF, Szwergold BS, Kappler F, Benesi AJ: Structural studies of a phosphocholine substituted beta-(1,3);(1,6) macrocyclic glucan from Bradyrhizobium japonicum USDA 110. Biochimica et biophysica acta. 1992, 1116 (3): 215-225.
Jelsma J, Kreger DR: Ultrastructural observations on (1 leads to 3)-beta-D-glucan from fungal cell-walls. Carbohydrate research. 1975, 43 (1): 200-203. 10.1016/S0008-6215(00)83988-9.
Marszalek PE, Li H, Fernandez JM: Fingerprinting polysaccharides with single-molecule atomic force microscopy. Nature biotechnology. 2001, 19 (3): 258-262. 10.1038/85712.
Dixon DR, Darveau RP: Lipopolysaccharide heterogeneity: innate host responses to bacterial modification of lipid a structure. J Dent Res. 2005, 84 (7): 584-595. 10.1177/154405910508400702.
Gaffin SL: Endotoxin determination in viscous opaque solutions of iron dextran by Limulus amebocyte lysate. Progress in clinical and biological research. 1979, 29: 221-227.
Knudsen KE, Jensen BB, Hansen I: Digestion of polysaccharides and other major components in the small and large intestine of pigs fed on diets consisting of oat fractions rich in beta-D-glucan. Br J Nutr. 1993, 70 (2): 537-556. 10.1079/BJN19930147.
Ohno N, Terui T, Chiba N, Kurachi K, Adachi Y, Yadomae T: Resistance of highly branched (1-->3)-beta-D-glucans to formolysis. Chem Pharm Bull (Tokyo). 1995, 43 (6): 1057-1060.
Wang H, Weening D, Jonkers E, Boer T, Stellaard F, Small AC, Preston T, Vonk RJ, Priebe MG: A curve fitting approach to estimate the extent of fermentation of indigestible carbohydrates. Eur J Clin Invest. 2008, 38 (11): 863-868.
Vos A, M'Rabet L, Stahl B, Boehm G, Garssen J: Immune-modulatory effects and potential working mechanisms of orally applied nondigestible carbohydrates. Crit Rev Immunol. 2007, 27 (2): 97-140.
Vetvicka V, Dvorak B, Vetvickova J, Richter J, Krizan J, Sima P, Yvin JC: Orally administered marine (1-->3)-beta-D-glucan Phycarine stimulates both humoral and cellular immunity. Int J Biol Macromol. 2007, 40 (4): 291-298. 10.1016/j.ijbiomac.2006.08.009.
Rice PJ, Lockhart BE, Barker LA, Adams EL, Ensley HE, Williams DL: Pharmacokinetics of fungal (1–3)-beta-D-glucans following intravenous administration in rats. Int Immunopharmacol. 2004, 4 (9): 1209-1215. 10.1016/j.intimp.2004.05.013.
Hong F, Yan J, Baran JT, Allendorf DJ, Hansen RD, Ostroff GR, Xing PX, Cheung NK, Ross GD: Mechanism by which orally administered beta-1,3-glucans enhance the tumoricidal activity of antitumor monoclonal antibodies in murine tumor models. J Immunol. 2004, 173 (2): 797-806.
Rice PJ, Adams EL, Ozment-Skelton T, Gonzalez AJ, Goldman MP, Lockhart BE, Barker LA, Breuel KF, Deponti WK, Kalbfleisch JH: Oral delivery and gastrointestinal absorption of soluble glucans stimulate increased resistance to infectious challenge. The Journal of pharmacology and experimental therapeutics. 2005, 314 (3): 1079-1086. 10.1124/jpet.105.085415.
Lehne G, Haneberg B, Gaustad P, Johansen PW, Preus H, Abrahamsen TG: Oral administration of a new soluble branched beta-1,3-D-glucan is well tolerated and can lead to increased salivary concentrations of immunoglobulin A in healthy volunteers. Clin Exp Immunol. 2006, 143 (1): 65-69. 10.1111/j.1365-2249.2005.02962.x.
Sun L, Zhao Y: The biological role of dectin-1 in immune response. International reviews of immunology. 2007, 26 (5–6): 349-364. 10.1080/08830180701690793.
Brown GD, Herre J, Williams DL, Willment JA, Marshall AS, Gordon S: Dectin-1 mediates the biological effects of beta-glucans. The Journal of experimental medicine. 2003, 197 (9): 1119-1124. 10.1084/jem.20021890.
Herre J, Gordon S, Brown GD: Dectin-1 and its role in the recognition of beta-glucans by macrophages. Molecular immunology. 2004, 40 (12): 869-876. 10.1016/j.molimm.2003.10.007.
Schorey JS, Lawrence C: The pattern recognition receptor Dectin-1: from fungi to mycobacteria. Curr Drug Targets. 2008, 9 (2): 123-129. 10.2174/138945008783502430.
Brown GD: Dectin-1: a signalling non-TLR pattern-recognition receptor. Nat Rev Immunol. 2006, 6 (1): 33-43. 10.1038/nri1745.
Taylor PR, Brown GD, Reid DM, Willment JA, Martinez-Pomares L, Gordon S, Wong SY: The beta-glucan receptor, dectin-1, is predominantly expressed on the surface of cells of the monocyte/macrophage and neutrophil lineages. J Immunol. 2002, 169 (7): 3876-3882.
Gantner BN, Simmons RM, Canavera SJ, Akira S, Underhill DM: Collaborative induction of inflammatory responses by dectin-1 and Toll-like receptor 2. The Journal of experimental medicine. 2003, 197 (9): 1107-1117. 10.1084/jem.20021787.
Herre J, Marshall AS, Caron E, Edwards AD, Williams DL, Schweighoffer E, Tybulewicz V, Reis e Sousa C, Gordon S, Brown GD: Dectin-1 uses novel mechanisms for yeast phagocytosis in macrophages. Blood. 2004, 104 (13): 4038-4045. 10.1182/blood-2004-03-1140.
Goodridge HS, Simmons RM, Underhill DM: Dectin-1 stimulation by Candida albicans yeast or zymosan triggers NFAT activation in macrophages and dendritic cells. J Immunol. 2007, 178 (5): 3107-3115.
Gross O, Gewies A, Finger K, Schafer M, Sparwasser T, Peschel C, Forster I, Ruland J: Card9 controls a non-TLR signalling pathway for innate anti-fungal immunity. Nature. 2006, 442 (7103): 651-656. 10.1038/nature04926.
Rogers NC, Slack EC, Edwards AD, Nolte MA, Schulz O, Schweighoffer E, Williams DL, Gordon S, Tybulewicz VL, Brown GD: Syk-dependent cytokine induction by Dectin-1 reveals a novel pattern recognition pathway for C type lectins. Immunity. 2005, 22 (4): 507-517. 10.1016/j.immuni.2005.03.004.
Taylor PR, Brown GD, Herre J, Williams DL, Willment JA, Gordon S: The role of SIGNR1 and the beta-glucan receptor (dectin-1) in the nonopsonic recognition of yeast by specific macrophages. J Immunol. 2004, 172 (2): 1157-1162.
Lin YL, Liang YC, Lee SS, Chiang BL: Polysaccharide purified from Ganoderma lucidum induced activation and maturation of human monocyte-derived dendritic cells by the NF-kappaB and p38 mitogen-activated protein kinase pathways. J Leukoc Biol. 2005, 78 (2): 533-543. 10.1189/jlb.0804481.
Rice PJ, Kelley JL, Kogan G, Ensley HE, Kalbfleisch JH, Browder IW, Williams DL: Human monocyte scavenger receptors are pattern recognition receptors for (1-->3)-beta-D-glucans. J Leukoc Biol. 2002, 72 (1): 140-146.
Sato T, Iwabuchi K, Nagaoka I, Adachi Y, Ohno N, Tamura H, Seyama K, Fukuchi Y, Nakayama H, Yoshizaki F: Induction of human neutrophil chemotaxis by Candida albicans-derived beta-1,6-long glycoside side-chain-branched beta-glucan. J Leukoc Biol. 2006, 80 (1): 204-211. 10.1189/jlb.0106069.
Chan WK, Law HK, Lin ZB, Lau YL, Chan GC: Response of human dendritic cells to different immunomodulatory polysaccharides derived from mushroom and barley. Int Immunol. 2007, 19 (7): 891-899. 10.1093/intimm/dxm061.
Lin YL, Lee SS, Hou SM, Chiang BL: Polysaccharide purified from Ganoderma lucidum induces gene expression changes in human dendritic cells and promotes T helper 1 immune response in BALB/c mice. Mol Pharmacol. 2006, 70 (2): 637-644. 10.1124/mol.106.022327.
Bohn J, BeMiller J: (1->3)-β-Glucans as biological response modifiers: a review of structure-functional activity relationships. Carbohydrate Polymers. 1995, 28 (1): 3-14. 10.1016/0144-8617(95)00076-3.
Cobb BA, Wang Q, Tzianabos AO, Kasper DL: Polysaccharide processing and presentation by the MHCII pathway. Cell. 2004, 117 (5): 677-687. 10.1016/j.cell.2004.05.001.
Karumuthil-Melethil S, Perez N, Li R, Vasu C: Induction of innate immune response through TLR2 and dectin 1 prevents type 1 diabetes. J Immunol. 2008, 181 (12): 8323-8334.
Klein E, Di Renzo L, Yefenof E: Contribution of CR3, CD11b/CD18 to cytolysis by human NK cells. Molecular immunology. 1990, 27 (12): 1343-1347. 10.1016/0161-5890(90)90041-W.
Di Renzo L, Yefenof E, Klein E: The function of human NK cells is enhanced by beta-glucan, a ligand of CR3 (CD11b/CD18). European journal of immunology. 1991, 21 (7): 1755-1758. 10.1002/eji.1830210726.
Cheung NK, Modak S, Vickers A, Knuckles B: Orally administered beta-glucans enhance anti-tumor effects of monoclonal antibodies. Cancer Immunol Immunother. 2002, 51 (10): 557-564.
Modak S, Koehne G, Vickers A, O'Reilly RJ, Cheung NK: Rituximab therapy of lymphoma is enhanced by orally administered (1-->3),(1-->4)-D-beta-glucan. Leuk Res. 2005, 29 (6): 679-683. 10.1016/j.leukres.2004.10.008.
Dushkin MI, Safina AF, Vereschagin EI, Schwartz Y: Carboxymethylated beta-1,3-glucan inhibits the binding and degradation of acetylated low density lipoproteins in macrophages in vitro and modulates their plasma clearance in vivo. Cell Biochem Funct. 1996, 14 (3): 209-217.
Zimmerman JW, Lindermuth J, Fish PA, Palace GP, Stevenson TT, DeMong DE: A novel carbohydrate-glycosphingolipid interaction between a beta-(1–3)-glucan immunomodulator, PGG-glucan, and lactosylceramide of human leukocytes. The Journal of biological chemistry. 1998, 273 (34): 22014-22020. 10.1074/jbc.273.34.22014.
Iwabuchi K, Nagaoka I: Lactosylceramide-enriched glycosphingolipid signaling domain mediates superoxide generation from human neutrophils. Blood. 2002, 100 (4): 1454-1464.
Vereschagin EI, van Lambalgen AA, Dushkin MI, Schwartz YS, Polyakov L, Heemskerk A, Huisman E, Thijs LG, van den Bos GC: Soluble glucan protects against endotoxin shock in the rat: the role of the scavenger receptor. Shock (Augusta, Ga). 1998, 9 (3): 193-198.
Wakshull E, Brunke-Reese D, Lindermuth J, Fisette L, Nathans RS, Crowley JJ, Tufts JC, Zimmerman J, Mackin W, Adams DS: PGG-glucan, a soluble beta-(1,3)-glucan, enhances the oxidative burst response, microbicidal activity, and activates an NF-kappa B-like factor in human PMN: evidence for a glycosphingolipid beta-(1,3)-glucan receptor. Immunopharmacology. 1999, 41 (2): 89-107. 10.1016/S0162-3109(98)00059-9.
Tang W, Liu JW, Zhao WM, Wei DZ, Zhong JJ: Ganoderic acid T from Ganoderma lucidum mycelia induces mitochondria mediated apoptosis in lung cancer cells. Life Sci. 2006, 80 (3): 205-211. 10.1016/j.lfs.2006.09.001.
Lin SB, Li CH, Lee SS, Kan LS: Triterpene-enriched extracts from Ganoderma lucidum inhibit growth of hepatoma cells via suppressing protein kinase C, activating mitogen-activated protein kinases and G2-phase cell cycle arrest. Life Sci. 2003, 72 (21): 2381-2390. 10.1016/S0024-3205(03)00124-3.
Min BS, Gao JJ, Nakamura N, Hattori M: Triterpenes from the spores of Ganoderma lucidum and their cytotoxicity against meth-A and LLC tumor cells. Chem Pharm Bull (Tokyo). 2000, 48 (7): 1026-1033.
Muller CI, Kumagai T, O'Kelly J, Seeram NP, Heber D, Koeffler HP: Ganoderma lucidum causes apoptosis in leukemia, lymphoma and multiple myeloma cells. Leukemia research. 2006, 30 (7): 841-848. 10.1016/j.leukres.2005.12.004.
Chan WKD, Cheung CC, Law HKD, Lau YLD, Chan GCD: Ganoderma lucidum polysaccharides can induce human monocytic leukemia cells into dendritic cells with immuno-stimulatory function. J Hematol Oncol. 2008, 1 (1): 9-10.1186/1756-8722-1-9.
Demir G, Klein HO, Mandel-Molinas N, Tuzuner N: Beta glucan induces proliferation and activation of monocytes in peripheral blood of patients with advanced breast cancer. Int Immunopharmacol. 2007, 7 (1): 113-116. 10.1016/j.intimp.2006.08.011.
Kidd PM: The use of mushroom glucans and proteoglycans in cancer treatment. Altern Med Rev. 2000, 5 (1): 4-27.
Miyakoshi H, Aoki T, Mizukoshi M: Acting mechanisms of Lentinan in human – II. Enhancement of non-specific cell-mediated cytotoxicity as an interferon inducer. International journal of immunopharmacology. 1984, 6 (4): 373-379. 10.1016/0192-0561(84)90057-2.
Kawaoka T, Yoshino S, Hazama S, Tangoku A, Oka M: [Clinical evaluation of intrapleural or peritoneal administration of lentinan and OK-432 for malignant effusion]. Gan to kagaku ryoho. 2003, 30 (11): 1562-1565.
Nakano H, Namatame K, Nemoto H, Motohashi H, Nishiyama K, Kumada K: A multi-institutional prospective study of lentinan in advanced gastric cancer patients with unresectable and recurrent diseases: effect on prolongation of survival and improvement of quality of life. Kanagawa Lentinan Research Group. Hepato-gastroenterology. 1999, 46 (28): 2662-2668.
Nakano T, Oka K, Hanba K, Morita S: Intratumoral administration of sizofiran activates Langerhans cell and T-cell infiltration in cervical cancer. Clinical immunology and immunopathology. 1996, 79 (1): 79-86. 10.1006/clin.1996.0053.
Kano Y, Kakuta H, Hashimoto J: Effect of sizofiran on regional lymph nodes in patients with head and neck cancer. Biotherapy (Dordrecht, Netherlands). 1996, 9 (4): 257-262.
Inoue M, Tanaka Y, Sugita N, Yamasaki M, Yamanaka T, Minagawa J, Nakamuro K, Tani T, Okudaira Y, Karita T: Improvement of long-term prognosis in patients with ovarian cancers by adjuvant sizofiran immunotherapy: a prospective randomized controlled study. Biotherapy (Dordrecht, Netherlands). 1993, 6 (1): 13-18.
Kodama N, Komuta K, Nanba H: Can maitake MD-fraction aid cancer patients?. Altern Med Rev. 2002, 7 (3): 236-239.
Kodama N, Komuta K, Nanba H: Effect of Maitake (Grifola frondosa) D-Fraction on the activation of NK cells in cancer patients. J Med Food. 2003, 6 (4): 371-377. 10.1089/109662003772519949.
Black W: Several apparent errors surfaced on reading the article in the June 2002 issue of Alternative Medicine Review by Kodama et al. entitled "Can maitake MD-fraction aid cancer patients"?. Altern Med Rev. 2002, 7 (6): 451-
Fisher M, Yang LX: Anticancer effects and mechanisms of polysaccharide-K (PSK): implications of cancer immunotherapy. Anticancer Res. 2002, 22 (3): 1737-1754.
Hayakawa K, Mitsuhashi N, Saito Y, Nakayama Y, Furuta M, Nakamoto S, Kawashima M, Niibe H: Effect of Krestin as adjuvant treatment following radical radiotherapy in non-small cell lung cancer patients. Cancer Detect Prev. 1997, 21 (1): 71-77.
Sakamoto J, Nakazato H: [Evaluation of adjuvant immunochemotherapy in advanced gastric cancer]. Gan to kagaku ryoho. 1993, 20 (16): 2525-2530.
Ohno R, Yamada K, Masaoka T, Ohshima T, Amaki I, Hirota Y, Horikoshi N, Horiuchi A, Imai K, Kimura I: A randomized trial of chemoimmunotherapy of acute nonlymphocytic leukemia in adults using a protein-bound polysaccharide preparation. Cancer Immunol Immunother. 1984, 18 (3): 149-154. 10.1007/BF00205503.
Nishiwaki Y, Furuse K, Fukuoka M, Ota M, Niitani H, Asakawa M, Nakai H, Sakai S, Ogawa N: [A randomized controlled study of PSK combined immuno-chemotherapy for adenocarcinoma of the lung. The Advanced Lung Cancer Immuno-chemotherapy Study Group]. Gan to kagaku ryoho. 1990, 17 (1): 131-136.
Go P, Chung CH: Adjuvant PSK immunotherapy in patients with carcinoma of the nasopharynx. The Journal of international medical research. 1989, 17 (2): 141-149.
Gao Y, Tang W, Dai X, Gao H, Chen G, Ye J, Chan E, Koh HL, Li X, Zhou S: Effects of water-soluble Ganoderma lucidum polysaccharides on the immune functions of patients with advanced lung cancer. J Med Food. 2005, 8 (2): 159-168. 10.1089/jmf.2005.8.159.
Chen X, Hu ZP, Yang XX, Huang M, Gao Y, Tang W, Chan SY, Dai X, Ye J, Ho PC: Monitoring of immune responses to a herbal immuno-modulator in patients with advanced colorectal cancer. Int Immunopharmacol. 2006, 6 (3): 499-508. 10.1016/j.intimp.2005.08.026.
Chen J, Seviour R: Medicinal importance of fungal beta-(1-->3), (1-->6)-glucans. Mycol Res. 2007, 111 (Pt 6): 635-652. 10.1016/j.mycres.2007.02.011.
We would like to thank Dr. Anita Chan (U. Alberta) for the English editing, Mr. Spencer Ng for the production of the graphic figures, the Edward Sai-Kim Hotung Paediatric Education & Research Fund, URC/CRCG Grants and Pau Kwong Wun Charitable Foundation for supporting the beta-glucan related works.
The authors declare that there is no conflict of interests, including conflicts of financial nature involving any pharmaceutical or commercial company.
GCFC initiated the concept, wrote and revised the manuscript and creating the illustrations. WKC involved in writing, coordination and revising the manuscript. DMS involved in the preparation and revision of manuscript.
About this article
Cite this article
Chan, G.CF., Chan, W.K. & Sze, D.MY. The effects of β-glucan on human immune and cancer cells. J Hematol Oncol 2, 25 (2009). https://doi.org/10.1186/1756-8722-2-25