共 90 条
Early events governing memory CD8+ T-cell differentiation
被引:61
作者:

Obar, Joshua J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Connecticut, Ctr Hlth, Dept Immunol, Ctr Integrated Immunol & Vaccine Res, Farmington, CT 06030 USA Univ Connecticut, Ctr Hlth, Dept Immunol, Ctr Integrated Immunol & Vaccine Res, Farmington, CT 06030 USA

Lefrancois, Leo
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h-index: 0
机构:
Univ Connecticut, Ctr Hlth, Dept Immunol, Ctr Integrated Immunol & Vaccine Res, Farmington, CT 06030 USA Univ Connecticut, Ctr Hlth, Dept Immunol, Ctr Integrated Immunol & Vaccine Res, Farmington, CT 06030 USA
机构:
[1] Univ Connecticut, Ctr Hlth, Dept Immunol, Ctr Integrated Immunol & Vaccine Res, Farmington, CT 06030 USA
基金:
美国国家卫生研究院;
关键词:
CD8 T cell;
CTL;
differentiation;
memory;
DENDRITIC CELLS;
IN-VIVO;
INFLAMMATORY CYTOKINES;
INTERLEUKIN-7;
RECEPTOR;
ANTIGEN PRESENTATION;
SECONDARY EXPANSION;
EFFECTOR PHENOTYPE;
CD8-T-CELL MEMORY;
CLONAL EXPANSION;
CD4-T-CELL HELP;
D O I:
10.1093/intimm/dxq053
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Understanding the regulation of the CD8(+) T-cell response and how protective memory cells are generated has been intensely studied. It is now appreciated that a naive CD8(+) T cell requires at least three signals to mount an effective immune response: (i) TCR triggering, (ii) co-stimulation and (iii) inflammatory cytokines. Only recently have we begun to understand the molecular integration of those signals and how early events regulate the fate decisions of the responding CD8(+) T cells. This review will discuss the recent findings about both the extracellular and intracellular factors that regulate the destiny of responding CD8(+) T cells.
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页码:619 / 625
页数:7
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