Signaling control of memory T cell generation and function

被引:54
作者
Chandok, MR [1 ]
Farber, DL [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Surg, Div Transplantat, Baltimore, MD 21201 USA
关键词
T lymphocytes; T cell-receptors; cellular differentiation; signal transduction; tyrosine kinase;
D O I
10.1016/j.smim.2004.08.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory T cells exhibit low activation thresholds and mediate rapid effector responses when recalled by antigen; contrasting the higher activation threshold, slower responses and predominant IL-2 production by naive T cells. While the sequence of intracellular events coupling the T cell-receptor (TCR) to naive T cell activation is well characterized, biochemical control of memory T cell differentiation and function remains undefined. In this review, we will discuss recent developments in T cell-receptor signal transduction as they pertain to memory T cells, and will discuss how signal dampening may drive memory generation, and more efficient spatial organization of signaling molecules may promote rapid recall responses. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:285 / 293
页数:9
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