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灵芝含岩藻糖多糖的免疫诱导抗体与肿瘤相关的 Globo H 系列表位。

Immunization of fucose-containing polysaccharides from Reishi mushroom induces antibodies to tumor-associated Globo H-series epitopes.

机构信息

Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan.

出版信息

Proc Natl Acad Sci U S A. 2013 Aug 20;110(34):13809-14. doi: 10.1073/pnas.1312457110. Epub 2013 Aug 1.

Abstract

Carbohydrate-based vaccines have shown therapeutic efficacy for infectious disease and cancer. The mushroom Ganoderma lucidum (Reishi) containing complex polysaccharides has been used as antitumor supplement, but the mechanism of immune response has rarely been studied. Here, we show that the mice immunized with a l-fucose (Fuc)-enriched Reishi polysaccharide fraction (designated as FMS) induce antibodies against murine Lewis lung carcinoma cells, with increased antibody-mediated cytotoxicity and reduced production of tumor-associated inflammatory mediators (in particular, monocyte chemoattractant protein-1). The mice showed a significant increase in the peritoneal B1 B-cell population, suggesting FMS-mediated anti-glycan IgM production. Furthermore, the glycan microarray analysis of FMS-induced antisera displayed a high specificity toward tumor-associated glycans, with the antigenic structure located in the nonreducing termini (i.e., Fucα1-2Galβ1-3GalNAc-R, where Gal, GalNAc, and R represent, respectively, D-galactose, D-N-acetyl galactosamine, and reducing end), typically found in Globo H and related tumor antigens. The composition of FMS contains mainly the backbone of 1,4-mannan and 1,6-α-galactan and through the Fucα1-2Gal, Fucα1-3/4Man, Fucα1-4Xyl, and Fucα1-2Fuc linkages (where Man and Xyl represent d-mannose and d-xylose, respectively), underlying the molecular basis of the FMS-induced IgM antibodies against tumor-specific glycans.

摘要

基于碳水化合物的疫苗已显示出治疗传染病和癌症的疗效。含有复杂多糖的药用真菌灵芝(Reishi)已被用作抗肿瘤补充剂,但免疫反应的机制很少被研究。在这里,我们表明,用富含 l-岩藻糖(Fuc)的灵芝多糖部分(命名为 FMS)免疫的小鼠诱导针对小鼠 Lewis 肺癌细胞的抗体,抗体介导的细胞毒性增加,肿瘤相关炎症介质的产生减少(特别是单核细胞趋化蛋白-1)。小鼠腹膜 B1 B 细胞群显著增加,表明 FMS 介导的抗糖 IgM 产生。此外,FMS 诱导的抗血清的糖芯片分析显示对肿瘤相关糖具有高特异性,抗原结构位于非还原末端(即,Fucα1-2Galβ1-3GalNAc-R,其中 Gal、GalNAc 和 R 分别代表 D-半乳糖、D-N-乙酰半乳糖胺和还原端),通常存在于 Globo H 和相关肿瘤抗原中。FMS 的组成主要包含 1,4-甘露聚糖和 1,6-α-半乳糖的主链,通过 Fucα1-2Gal、Fucα1-3/4Man、Fucα1-4Xyl 和 Fucα1-2Fuc 键(其中 Man 和 Xyl 分别代表 d-甘露糖和 d-木糖),为 FMS 诱导针对肿瘤特异性糖的 IgM 抗体提供了分子基础。

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