Revival of CD8+ Treg-mediated suppression

被引:157
|
作者
Smith, Trevor R. F. [1 ]
Kumar, Vipin [1 ]
机构
[1] Torrey Pines Inst Mol Studies, Lab Autoimmun, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.it.2008.04.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite their first recognition almost 40 years ago, CD8(+) 'suppressor' T cells remain poorly characterized. Recent studies of these lymphocytes, now popularly referred to as regulatory CD8(+) T cells (CD8(+) Tregs), have helped clarify their important role in the regulation of autoimmune disease. Here, we review progress related to the identification, phenotype and function of CD8(+) Tregs. We also focus on a newly described subset, CD8 alpha alpha(+) T-CR alpha beta(+) Tregs, which in mice recognize a T-cell receptor-derived peptide in the context of the class Ib major histocompatibility complex molecule Qa-1. These Tregs target only activated T cells and complement the suppression provided by CD4(+)Foxp3(+) Tregs. Investigations leading to the detailed identification, expansion, maintenance and function of CD alpha alpha(+) Tregs should result in new therapeutic strategies for human inflammatory diseases.
引用
收藏
页码:337 / 342
页数:6
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