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淋巴因子激活的小鼠巨噬细胞对曼氏血吸虫童虫的体外杀伤作用。

In vitro killing of S. mansoni schistosomula by lymphokine-activated mouse macrophages.

作者信息

Bout D T, Joseph M, David J R, Capron A R

出版信息

J Immunol. 1981 Jul;127(1):1-5.

PMID:7240738
Abstract

Inflammatory macrophages from mice i.p. injected with FCS 24-hr before harvesting, activated by partly purified MAF from Con A-stimulated spleen cells, were shown to kill an average of 60.9% (SE +/- 5.3) of the parasites in cultures of Schistosoma mansoni schistosomula. On the contrary, resident macrophages were not cytotoxic under the same conditions. The degree of macrophage activation for the killing was dependent upon both lymphokine concentration and time of incubation in lymphokine. The capacity of macrophages to be activated to kill schistosomula as well as the schistosomulicidal activity of the lymphokine-activated macrophages were short-lived properties. The killing was strongly influenced by the effector-to-target ratio. The results are consistent with other data on the immune response in experimental infection and particularly the development of the delayed hypersensitivity. Therefore, among the immune mechanisms that participate in immunity to reinfection, cell-mediated immunity that involves inflammatory macrophages should no longer be restricted to microorganisms and protozoans and could be extended to multicellular parasites like schistosomes.

摘要

在收获前24小时经腹腔注射胎牛血清的小鼠体内获取的炎性巨噬细胞,用来自经刀豆蛋白A刺激的脾细胞的部分纯化巨噬细胞活化因子激活后,在曼氏血吸虫童虫培养物中可杀死平均60.9%(标准误±5.3)的寄生虫。相反,在相同条件下,驻留巨噬细胞没有细胞毒性。巨噬细胞杀伤激活的程度取决于淋巴因子浓度和在淋巴因子中孵育的时间。巨噬细胞被激活以杀伤童虫的能力以及淋巴因子激活的巨噬细胞的杀童虫活性都是短暂的特性。杀伤作用受效应细胞与靶细胞比例的强烈影响。这些结果与实验性感染中免疫反应的其他数据一致,特别是迟发型超敏反应的发展。因此,在参与再感染免疫的免疫机制中,涉及炎性巨噬细胞的细胞介导免疫不应再局限于微生物和原生动物,而可扩展到像血吸虫这样的多细胞寄生虫。

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