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慢性HIV感染期间抗病毒细胞毒性淋巴细胞通过CD95(FAS/APO-1)介导途径产生的潜在有害作用。

Potential deleterious effect of anti-viral cytotoxic lymphocyte through the CD95 (FAS/APO-1)-mediated pathway during chronic HIV infection.

作者信息

Garcia S, Fevrier M, Dadaglio G, Lecoeur H, Riviere Y, Gougeon M L

机构信息

Unitè d'Oncologie Virale, Institut Pasteur, Paris, France.

出版信息

Immunol Lett. 1997 Jun 1;57(1-3):53-8. doi: 10.1016/s0165-2478(97)00070-9.

Abstract

The potential deleterious effect through a CD95-based pathway of anti-viral cytotoxic lymphocyte (CTL) during HIV-infection was studied. The present paper reports that a Nef specific CTL line derived from an HIV-infected person is able to kill not only Nef-expressing target cells but also CD95+ compliant Jurkat cells. The two mechanisms of cytotoxicity, i.e. perforin-vs-CD95-dependent were differentiated according to their respective Ca(2+)-dependence. The existence of the dual killing machinery in the anti-HIV CTL line was correlated with the coexpression in these cells of perforin and CD95-L molecules. A model of AIDS pathogenesis involving the deleterious effect through the CD95 pathway of the viral specific CTL response is discussed.

摘要

研究了在HIV感染期间通过基于CD95的抗病毒细胞毒性淋巴细胞(CTL)途径产生的潜在有害作用。本文报道,从一名HIV感染者衍生出的Nef特异性CTL系不仅能够杀死表达Nef的靶细胞,还能杀死CD95+的依从性Jurkat细胞。根据它们各自对Ca(2+)的依赖性,区分了两种细胞毒性机制,即穿孔素依赖性和CD95依赖性。抗HIV CTL系中双重杀伤机制的存在与这些细胞中穿孔素和CD95-L分子的共表达相关。本文讨论了一种艾滋病发病机制模型,该模型涉及病毒特异性CTL反应通过CD95途径产生的有害作用。

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