Transcriptional control of effector and memory CD8+ T cell differentiation

被引:1171
作者
Kaech, Susan M. [1 ,2 ]
Cui, Weiguo [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家卫生研究院;
关键词
CHEMOKINE RECEPTOR CXCR3; CHRONIC VIRAL-INFECTION; CUTTING EDGE; IN-VIVO; TERMINAL DIFFERENTIATION; MITOCHONDRIAL STAT3; PROTECTIVE IMMUNITY; LINEAGE COMMITMENT; CLONAL EXPANSION; VIRUS-INFECTION;
D O I
10.1038/nri3307
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During an infection, T cells can differentiate into multiple types of effector and memory T cells, which help to mediate pathogen clearance and provide long-term protective immunity. These cells can vary in their phenotype, function and location, and in their long-term fate in terms of their ability to populate the memory T cell pool. Over the past decade, the signalling pathways and transcriptional programmes that regulate the formation of heterogeneous populations of effector and memory CD8(+) T cells have started to be characterized, and this Review discusses the major advances in these areas.
引用
收藏
页码:749 / 761
页数:13
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