T-cell exhaustion: characteristics, causes and conversion

被引:488
作者
Yi, John S. [1 ]
Cox, Maureen A. [1 ]
Zajac, Allan J. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
chronic infections; cytokines; effector functions; inhibitory receptors; T cell exhaustion; C VIRUS-INFECTION; CHRONIC VIRAL-INFECTION; E3 UBIQUITIN LIGASE; PD-1; EXPRESSION; HEPATITIS-B; PROMOTER POLYMORPHISMS; SECONDARY EXPANSION; DISEASE PROGRESSION; IMMUNE-RESPONSES; TETRAMER BINDING;
D O I
10.1111/j.1365-2567.2010.03255.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
P>T-cell exhaustion is characterized by the stepwise and progressive loss of T-cell functions and can culminate in the physical deletion of the responding cells. Exhaustion is well-defined during chronic lymphocytic choriomeningitis virus infection and commonly develops under conditions of antigen-persistence, which occur following many chronic infections that are of significant public health concern including hepatitis B virus, hepatitis C virus and human immunodeficiency virus infections, as well as during tumour outgrowth. Exhaustion is not a uniformly disabled setting as a gradation of phenotypic and functional defects can manifest, and these cells are distinct from prototypic effector, memory and also anergic T cells. We are gaining insights into the extrinsic and intrinsic factors that determine the severity of exhaustion. These include the duration and magnitude of antigenic activation, availability of CD4 T-cell help, the levels of stimulatory and suppressive cytokines, as well as the expression of activatory and inhibitory receptors. More information is now becoming available regarding the molecular mechanisms that attenuate the responsiveness of exhausted T cells. As the parameters that dictate exhaustion are more thoroughly defined, this is fostering the development of methods that prevent and rejuvenate functionally inferior responses. In this article we discuss our current understanding of the properties of exhausted T cells and the mechanisms that promote and maintain this state.
引用
收藏
页码:474 / 481
页数:8
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