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表达恶性疟原虫MSP1-C的重组卡介苗(rBCG)刺激小鼠巨噬细胞系J774A.1后的吞噬活性及促炎细胞因子产生情况

Phagocytic activity and pro-inflammatory cytokines production by the murine macrophage cell line J774A.1 stimulated by a recombinant BCG (rBCG) expressing the MSP1-C of Plasmodium falciparum.

作者信息

Rapeah S, Dhaniah M, Nurul A A, Norazmi M N

机构信息

School of Health, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia.

出版信息

Trop Biomed. 2010 Dec;27(3):461-9.

Abstract

Macrophages are involved in innate immunity against malaria due to their ability to phagocytose infected erythrocytes and produce inflammatory cytokines, which are important for controlling parasite growth during malaria infection. In this study, the ability of a recombinant BCG (rBCG) vaccine expressing the 19-kDa C-terminus of merozoite surface protein-1 (MSP1-C) of Plasmodium falciparum, to stimulate the phagocytic activity and secretion of pro-inflammatory cytokines by the macrophage cell line J774A.1 was measured at varying times. The results demonstrate the ability of the rBCG construct to activate the inflammatory action of macrophages, which is important as a first-line of defence in clearing malaria infections.

摘要

巨噬细胞由于能够吞噬被感染的红细胞并产生炎性细胞因子,而参与针对疟疾的固有免疫,这些炎性细胞因子对于在疟疾感染期间控制寄生虫生长非常重要。在本研究中,测定了表达恶性疟原虫裂殖子表面蛋白-1(MSP1-C)19-kDa C末端的重组卡介苗(rBCG)疫苗在不同时间刺激巨噬细胞系J774A.1的吞噬活性和促炎细胞因子分泌的能力。结果证明了rBCG构建体激活巨噬细胞炎性作用的能力,这作为清除疟疾感染的第一道防线很重要。

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