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.