共 125 条
TCR Signaling in T Cell Memory
被引:77
作者:

Daniels, Mark A.
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机构:
Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA

Teixeiro, Emma
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h-index: 0
机构:
Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA
机构:
[1] Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA
关键词:
T cell receptor;
T cell;
protective immunity;
immune memory;
signaling;
NF-KAPPA-B;
CUTTING EDGE;
CD8(+) MEMORY;
TRANSCRIPTION FACTOR;
DIFFERENTIAL REQUIREMENT;
RECEPTOR REPERTOIRE;
MAMMALIAN TARGET;
PKC-THETA;
EFFECTOR;
CD4(+);
D O I:
10.3389/fimmu.2015.00617
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
T cell memory plays a critical role in our protection against pathogens and tumors. The antigen and its interaction with the T cell receptor (TCR) is one of the initiating elements that shape T cell memory together with inflammation and costimulation. Over the last decade, several transcription factors and signaling pathways that support memory programing have been identified. However, how TCR signals regulate them is still poorly understood. Recent studies have shown that the biochemical rules that govern T cell memory, strikingly, change depending on the TCR signal strength. Furthermore, TCR signal strength regulates the input of cytokine signaling, including pro-inflammatory cytokines. These highlight how tailoring antigenic signals can improve immune therapeutics. In this review, we focus on how TCR signaling regulates T cell memory and how the quantity and quality of TCR peptide MHC interactions impact the multiple fates a T cell can adopt in the memory pool.
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