Bias in the αβ T-cell repertoire: implications for disease pathogenesis and vaccination

被引:169
|
作者
Miles, John J. [1 ,2 ]
Douek, Daniel C. [3 ]
Price, David A. [1 ,3 ]
机构
[1] Cardiff Univ, T Cell Modulat Lab, Dept Infect Immun & Biochem, Sch Med, Cardiff CF14 4XN, Wales
[2] Queensland Inst Med Res, Cellular Immunol Lab, Dept Infect Dis & Immunol, Herston, Qld 4006, Australia
[3] NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
来源
IMMUNOLOGY AND CELL BIOLOGY | 2011年 / 89卷 / 03期
关键词
T cells; T-cell receptor; TCR repertoire; COMPLEX CLASS-I; ANTIGEN RECEPTOR GENES; MYELIN BASIC-PROTEIN; HUMAN CYTOMEGALOVIRUS; TCR-ALPHA; IMMUNE-RESPONSE; VIRUS TYPE-1; INFLUENZA-A; PREFERENTIAL EXPRESSION; LINKAGE DISEQUILIBRIUM;
D O I
10.1038/icb.2010.139
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The naive T-cell repertoire is vast, containing millions of unique T-cell receptor (TCR) structures. Faced with such diversity, the mobilization of TCR structures from this enormous pool was once thought to be a stochastic, even chaotic, process. However, steady and systematic dissection over the last 20 years has revealed that this is not the case. Instead, the TCR repertoire deployed against individual antigens is routinely ordered and biased. Often, identical and near-identical TCR repertoires can be observed across different individuals, suggesting that the system encompasses an element of predictability. This review provides a catalog of alpha beta TCR bias by disease and by species, and discusses the mechanisms that govern this inherent and widespread phenomenon. Immunology and Cell Biology (2011) 89, 375-387; doi:10.1038/icb.2010.139; published online 8 February 2011
引用
收藏
页码:375 / 387
页数:13
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