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猿猴γδ T细胞对肿瘤细胞和免疫缺陷病毒感染细胞的细胞毒性机制。

Mechanisms of simian gamma delta T cell cytotoxicity against tumor and immunodeficiency virus-infected cells.

作者信息

Gan Y H, Malkovsky M

机构信息

Department of Medical Microbiology and Immunology, University of Wisconsin-Madison 53706, USA.

出版信息

Immunol Lett. 1996 Mar;49(3):191-6. doi: 10.1016/0165-2478(96)02508-4.

Abstract

The mechanisms of cytotoxic killing of various tumor cell lines and immunodeficiency virus-infected T cell lines by simian gamma delta T cells were examined. The lysis of the majority of the target cell lines by gamma delta effectors was calcium-dependent, indicating that cytotoxicity is mediated by the perforin/granzyme pathway rather than the Fas-FasL pathway, with the exception of Jurkat cells. The gamma delta T cells were able to suppress SIV replication as measured by the p27 ELISA and the suppression was contact-dependent. We further determined that the target cells were induced to undergo apoptosis by the gamma delta T cell effectors. These results contribute to our understanding of the function of simian gamma delta T cells and their similarities to human gamma delta T cells, and extend our knowledge on the cytotoxic mechanisms employed by gamma delta T cells in general.

摘要

研究了猿猴γδT细胞对各种肿瘤细胞系和免疫缺陷病毒感染的T细胞系进行细胞毒性杀伤的机制。γδ效应细胞对大多数靶细胞系的裂解是钙依赖性的,这表明细胞毒性是由穿孔素/颗粒酶途径介导的,而不是Fas-FasL途径,但Jurkat细胞除外。通过p27 ELISA检测发现,γδT细胞能够抑制SIV复制,且这种抑制是接触依赖性的。我们进一步确定,γδT细胞效应器可诱导靶细胞发生凋亡。这些结果有助于我们了解猿猴γδT细胞的功能及其与人类γδT细胞的相似性,并扩展了我们对γδT细胞一般采用的细胞毒性机制的认识。

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