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避开死亡之吻:HIV及其他慢性病毒是如何存活的。

Avoiding the kiss of death: how HIV and other chronic viruses survive.

作者信息

Lieberman Judy, Manjunath N, Shankar Premlata

机构信息

Center for Blood Research and Department of Pediatrics, Harvard Medical School, 800 Huntington Avenue, Boston, MA 02115, USA.

出版信息

Curr Opin Immunol. 2002 Aug;14(4):478-86. doi: 10.1016/s0952-7915(02)00366-7.

Abstract

Virus-specific CD8 T cells during chronic infection often exceed in numbers virus-replicating infected cells. Why then do antiviral CD8 T cells not do a better job of controlling infection? Although viral strategies for immune evasion are well known, this review will focus on changes in the CD8 T cell that interfere with cytolytic function. Most antiviral CD8 T cells in chronic infection do not express perforin, a molecule that is required for cytolysis. IL-2 and other costimulatory signals can restore cytotoxicity that has been impaired, suggesting a role for CD4 T cell anergy. The chance to eradicate an infection by T cell mediated lysis is undermined after an infection becomes established, in part because the effector immune response is impaired in the setting of chronic antigen.

摘要

在慢性感染期间,病毒特异性CD8 T细胞的数量常常超过进行病毒复制的受感染细胞。那么,抗病毒CD8 T细胞为何不能更好地控制感染呢?尽管病毒的免疫逃逸策略已广为人知,但本综述将聚焦于CD8 T细胞中干扰细胞溶解功能的变化。慢性感染中的大多数抗病毒CD8 T细胞不表达穿孔素,而穿孔素是细胞溶解所必需的分子。白细胞介素-2和其他共刺激信号可恢复受损的细胞毒性,这表明CD4 T细胞无反应性发挥了作用。感染确立后,通过T细胞介导的裂解来根除感染的机会就会受到破坏,部分原因是在慢性抗原环境下效应免疫反应受损。

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