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Macrophage activation by polysaccharide biological response modifier isolated from Aloe vera L. var. chinensis (Haw.) Berg.

机译:分离自芦荟的多糖生物响应调节剂的巨噬细胞活化。中华Berg

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摘要

A mannose-rich polysaccharide biological response modifier (BRM), derived from Aloe vera L. var. chinensis (Haw.) Berg., was demonstrated to be a potent murine B- and T-cell stimulator in our previous study. We here report the stimulatory activity of PAC-I on murine peritoneal macrophage. The polysaccharide when injected into mice enhanced the migration of macrophages to the peritoneal cavity. Peritoneal macrophage when treated by PAC-I in vitro had increased expression of MHC-II and FcgammaR, and enhanced endocytosis, phagocytosis, nitric oxide production, TNF-alpha secretion and tumor cell cytotoxicity. The administration of PAC-I into allogeneic ICR mice stimulated systemic TNF-alpha production in a dose-dependent manner and prolonged the survival of tumor-bearing mice. PAC-I is thus a potent stimulator of murine macrophage and the in vitro observed tumoricidal properties of activated macrophage might account for the in vivo antitumor properties of PAC-I. Our research findings may have therapeutic implications in tumor immunotherapy.
机译:富含甘露糖的多糖生物反应调节剂(BRM),源自芦荟。在我们之前的研究中,中华小动物(Haw。)Berg。被证明是一种有效的小鼠B细胞和T细胞刺激剂。我们在这里报告PAC-I对小鼠腹膜巨噬细胞的刺激活性。当将多糖注射入小鼠体内时,可增强巨噬细胞向腹膜腔的迁移。腹腔巨噬细胞在体外用PAC-I处理时,MHC-II和FcgR的表达增加,并增强了内吞作用,吞噬作用,一氧化氮的产生,TNF-α的分泌和肿瘤细胞的细胞毒性。将PAC-I施用到同种异体ICR小鼠中,可以剂量依赖性方式刺激全身性TNF-α的产生,并延长了荷瘤小鼠的生存期。因此,PAC-1是鼠巨噬细胞的有效刺激剂,并且在体外观察到活化的巨噬细胞的杀肿瘤特性可能解释了PAC-1的体内抗肿瘤特性。我们的研究结果可能对肿瘤免疫治疗有治疗意义。

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