The effects of beta-glucan on human immune and cancer cells

• Published in: Journal of hematology and oncology Vol. 2; no. 1; p. 25
• Main Authors: Chan, Godfrey Chi-Fung, Chan, Wing Keung, Sze, Daniel Man-Yuen
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 10.06.2009; BioMed Central; BMC
• Subjects: Animals; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; beta-Glucans - administration & dosage; beta-Glucans - pharmacokinetics; beta-Glucans - pharmacology; Biological Products - administration & dosage; Cancer cells; Cell Proliferation - drug effects; Cell Survival - drug effects; Health aspects; Humans; Immune response; Immune System - drug effects; Immunologic Factors - administration & dosage; Immunologic Factors - pharmacokinetics; Immunologic Factors - pharmacology; Models, Biological; Neoplasms - drug therapy; Neoplasms - pathology; Physiological aspects; Review; Hong Kong
• ISSN: 1756-8722; 1756-8722
• DOI: 10.1186/1756-8722-2-25

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 beta-glucans. beta-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, beta-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 beta-glucans and they can also enhance opsonic and non-opsonic phagocytosis. In animal studies, after oral administration, the specific backbone 1-->3 linear beta-glycosidic chain of beta-glucans cannot be digested. Most beta-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 beta-glucans fragments are eventually released by the macrophages and taken up by other immune cells leading to various immune responses. However, beta-glucans of different sizes and branching patterns may have significantly variable immune potency. Careful selection of appropriate beta-glucans is essential if we wish to investigate the effects of beta-glucans clinically. So far, no good quality clinical trial data is available on assessing the effectiveness of purified beta-glucans among cancer patients. Future effort should direct at performing well-designed clinical trials to verify the actual clinical efficacy of beta-glucans or beta-glucans containing compounds.