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CD8 + 细胞毒性T细胞与利什曼原虫感染的巨噬细胞之间的相互作用。

The interaction between CD8+ cytotoxic T cells and Leishmania-infected macrophages.

作者信息

Smith L E, Rodrigues M, Russell D G

机构信息

Department of Pathology, New York University Medical Center, New York 10016.

出版信息

J Exp Med. 1991 Sep 1;174(3):499-505. doi: 10.1084/jem.174.3.499.

Abstract

Leishmania is resident within the macrophages of its vertebrate host. In any intramacrophage infection, where the pathogen is present in a form capable of mediating cell to cell transmission, the contribution of a cytotoxic T cell response to protective immunity is questionable. This study presents data from an in vitro model designed to elucidate the outcome of an interaction between CD8+, cytotoxic T cells and infected macrophages. Experiments were conducted with an H-2d-restricted, cytotoxic CD8+ T cell clone and Leishmania parasites present in mixed macrophage cultures, with the parasites confined to either histocompatible BALB/c macrophages, or incompatible CBA macrophages. Initial experiments indicated that the viability of Leishmania was unaffected by the lysis of its host macrophage by cytotoxic T cells. However, extended experiments showed that the parasites were killed between 24 and 72 h. The same results were obtained regardless of whether the parasites were resident in the target, BALB/c, macrophages or the bystander, CBA, macrophages. Addition of neutralizing, anti-IFN-g antibody to the cultures ablated most of the leishmanicidal behavior, indicating that parasite death was attributable to macrophage activation, resulting from cytokine secretion from the T cells following the initial recognition event.

摘要

利什曼原虫寄生于其脊椎动物宿主的巨噬细胞内。在任何巨噬细胞内感染中,若病原体以能够介导细胞间传播的形式存在,细胞毒性T细胞反应对保护性免疫的贡献就值得怀疑。本研究展示了来自体外模型的数据,该模型旨在阐明CD8 +细胞毒性T细胞与受感染巨噬细胞之间相互作用的结果。实验使用了一个H - 2d限制的细胞毒性CD8 + T细胞克隆以及混合巨噬细胞培养物中存在的利什曼原虫寄生虫,寄生虫被限制在组织相容性的BALB / c巨噬细胞或不相容的CBA巨噬细胞中。初步实验表明,细胞毒性T细胞对其宿主巨噬细胞的裂解并未影响利什曼原虫的活力。然而,进一步的实验表明,寄生虫在24至72小时内被杀死。无论寄生虫是存在于靶细胞BALB / c巨噬细胞还是旁观者CBA巨噬细胞中,都得到了相同的结果。向培养物中添加中和性抗IFN - g抗体消除了大部分杀利什曼原虫行为,表明寄生虫死亡归因于巨噬细胞活化,这是初始识别事件后T细胞分泌细胞因子所致。

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