Biochemical signaling pathways for memory T cell recall

被引:55
作者
Farber, Donna L. [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Surg, Baltimore, MD 21201 USA
关键词
T lymphocytes; T cell receptors; Signal transduction; Transcription factors; Innate immunity; NF-KAPPA-B; IFN-GAMMA PROMOTER; PROTEIN-TYROSINE KINASE; CUTTING EDGE; HISTONE ACETYLATION; FLOW-CYTOMETRY; LISTERIA-MONOCYTOGENES; INTERFERON-GAMMA; CLONAL EXPANSION; LYMPHOCYTES-T;
D O I
10.1016/j.smim.2009.02.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Memory T cells exhibit low activation thresholds and rapid effector responses following antigen stimulation, contrasting naive T cells with high activation thresholds and no effector responses. Signaling mechanisms for the distinct properties of naive and memory T cells remain poorly understood. Here, 1 will discuss new results on signal transduction in naive and memory T cells that suggest proximal control of activation threshold and a distinct biochemical pathway to rapid recall. The signaling and transcriptional pathways controlling immediate effector function in memory T cells closely resemble pathways for rapid effector cytokine production in innate immune cells, suggesting memory T cells use innate pathways for efficacious responses. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:84 / 91
页数:8
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