CD28 costimulation of developing thymocytes induces Foxp3 expression and regulatory T cell differentiation independently of interleukin 2

被引:485
作者
Tai, XG
Cowan, M
Feigenbaum, L
Singer, A [1 ]
机构
[1] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[2] NCI, SAIC Frederick, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA
关键词
D O I
10.1038/ni1160
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Efficient generation of regulatory T cells (T-reg cells) in the thymus requires CD28 costimulation, but it is not known why. Here, molecular mapping of CD28 costimulation showed that T-reg cell generation requires a motif that binds the tyrosine kinase Lck, precisely the same motif that is required for CD28 costimulation of interleukin 2 production. Nevertheless, CD28 costimulation provides more than interleukin 2 to developing T-reg cells, as CD28 costimulation of T cell receptor-signaled double-positive thymocytes induced expression of Foxp3, considered to be the T-reg 'master gene', as well as GITR and CTLA-4, two proteins expressed on T-reg cells. Thus, CD28 costimulation directly signals developing thymocytes to express Foxp3 and to initiate the T-reg cell differentiation program.
引用
收藏
页码:152 / 162
页数:11
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