T cell exhaustion during persistent viral infections

被引:245
作者
Kahan, Shannon M. [1 ]
Wherry, E. John [2 ,3 ]
Zajac, Allan J. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[2] Univ Penn, Perelman Sch Med, Inst Immunol, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Cytokines; Immunity; Inhibitory receptors; Persistent infections; T cell exhaustion; GROWTH-FACTOR-BETA; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; EXPRESS HIGH-LEVELS; PD-1; EXPRESSION; CUTTING EDGE; UP-REGULATION; NK CELLS; IMMUNE ACTIVATION; TIM-3; TETRAMER BINDING;
D O I
10.1016/j.virol.2014.12.033
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Although robust and highly effective anti-viral T cells contribute to the clearance of many acute infections, viral persistence is associated with the development of functionally inferior, exhausted, T cell responses. Exhaustion develops in a step-wise and progressive manner, ranges in severity, and can culminate in the deletion of the anti-viral T cells. This disarming of the response is consequential as it compromises viral control and potentially serves to dampen immune-mediated damage. Exhausted T cells are unable to elaborate typical anti-viral effector functions. They are characterized by the sustained upregulation of inhibitory receptors and display a gene expression profile that distinguishes them from prototypic effector and memory T cell populations. In this review we discuss the properties of exhausted T cells; the virological and immunological conditions that favor their development; the cellular and molecular signals that sustain the exhausted state; and strategies for preventing and reversing exhaustion to favor viral control. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:180 / 193
页数:14
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