CD4+CD25+ regulatory T cells in HIV infection

被引:32
|
作者
Nixon, DF [1 ]
Aandahl, EM [1 ]
Michaëlsson, J [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
关键词
CD4(+)CD25(+) regulatory T cells; FoxP3; HIV;
D O I
10.1016/j.micinf.2005.03.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system faces the difficult task of discerning between foreign, potentially pathogen-derived antigens and self-antigens. Several mechanisms, including deletion of self-reactive T cells in the thymus, have been shown to contribute to the acceptance of self-antigens and the reciprocal reactivity to foreign antigens. Over the last decade it has become increasingly clear that CD4(+)CD25(+) T-Reg cells are crucial for maintenance of T cell tolerance to self-antigens in the periphery, and to avoid development of autoimmune disorders. Recently, evidence has also emerged that demonstrates that CD4(+)CD25(+) T-Reg cells can also suppress T cell responses to foreign pathogens, including viruses such as HIV. In this article we review the current knowledge and potential role of CD4(+)CD25(+) T-Reg cells in HIV infection. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:1063 / 1065
页数:3
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