Immune biology of Ag-specific γδ T cells in infections

被引:30
作者
Chen, Zheng W. [1 ]
机构
[1] Univ Illinois, Coll Med Chicago, Dept Microbiol & Immunol, Ctr Primate Biomed Res, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
gamma delta T cells; T cell receptor; T cell responses; Human infections; Tuberculosis; Phosphoantigen; (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate (HMBPP); HIV; Pneumonic plague; IN-VIVO; (E)-4-HYDROXY-3-METHYL-BUT-2-ENYL PYROPHOSPHATE; MYCOBACTERIAL COINFECTION; V-GAMMA-2V-DELTA-2; TCR; TUBERCULOSIS INFECTION; ANTIGEN RECOGNITION; RESPONSES; PHOSPHOANTIGEN; EXPANSION; CYTOKINE;
D O I
10.1007/s00018-011-0703-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence suggests that human gamma delta T cells act as non-classical T cells and contribute to both innate and adaptive immune responses in infections. V gamma 2 V delta 2 T (also termed V gamma 9 V delta 2 T) cells exist only in primates, and in humans represent a dominant circulating gamma delta T-cell subset. Primate V gamma 2 V delta 2 T cells are the only gamma delta T cell subset capable of recognizing microbial phosphoantigen. Since nonhuman primate V gamma 2 V delta 2 T cells resemble their human counterparts, in-depth studies have been undertaken in macaques to understand the biology and function of human V gamma 2 V delta 2 T cells. This article reviews the recent progress for immune biology of V gamma 2 V delta 2 T cells in infections.
引用
收藏
页码:2409 / 2417
页数:9
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