Transcriptional regulation of effector and memory CD8+ T cell fates

被引:23
|
作者
Thaventhiran, James E. D. [1 ]
Fearon, Douglas T. [2 ,3 ]
Gattinoni, Luca [4 ]
机构
[1] Papworth Hosp NHS Fdn Trust, Ctr Lung Infect, Cambridge CB23 3RE, England
[2] Univ Cambridge, Dept Med, Sch Clin Med, Cambridge CB2 2QH, England
[3] Li Ka Shing Ctr, Canc Res UK Cambridge Res Inst, Cambridge CB2 0RE, England
[4] NCI, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 英国惠康基金;
关键词
CUTTING EDGE; BETA-CATENIN; DIFFERENTIATION; GENERATION; WNT; EXPRESSION; PATHWAY; ACTIVATION; BLIMP-1; ID2;
D O I
10.1016/j.coi.2013.05.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunity to intracellular pathogens and cancer relies on the generation of robust CD8(+) T cell effector responses as well as the establishment of immunological memory. During a primary immune response CD8(+) T cells experience diverse extracellular environmental cues and cell-cell interactions that trigger downstream transcriptional programs ultimately guiding a CD8(+) T cell to undertake either an effector or a memory cell fate. Here, we discuss our current understanding of the signaling pathways and transcriptional networks that regulate effector and memory commitment in CD8(+) T lymphocytes.
引用
收藏
页码:321 / 328
页数:8
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