The role of self-peptides in the development of CD4+ CD25+ regulatory T cells

被引:38
作者
Picca, CC [1 ]
Caton, AJ [1 ]
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.coi.2005.01.003
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 thymus produces a unique lineage of cells known as CD4(+) CD25(+) regulatory T cells, and the exact processes leading to their development continue to be defined. Highly specific interactions between developing thymocytes and cognate self-antigens expressed by radioresistant elements in the thymus have been shown to drive CD4(+) CD25(+) regulatory-T-cell development. The self-peptide(s) that mediate thymic selection of CD4(+) CD25(+) regulatory T cells can also promote their expansion in the periphery, and self-peptides might also play a role in the conversion of CD4(+) CD25(-) T cells into CD25(+) regulatory T cells.
引用
收藏
页码:131 / 136
页数:6
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