Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells

被引:996
作者
Battaglia, M
Stabilini, A
Roncarolo, MG
机构
[1] San Raffaele Telethon Inst Gene Therapy, HSR, TIGET, Milan, Italy
[2] Vita Salute San Raffaele Univ, Milan, Italy
关键词
D O I
10.1182/blood-2004-10-3932
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Rapamycin is an immunosuppressive compound that is currently used to prevent acute graft rejection in humans. In addition, rapamycin has been shown to allow operational tolerance in murine models. However, a direct effect of rapamycin on T regulatory (Tr) cells, which play a key role in induction and maintenance of peripheral tolerance, has not been demonstrated so far. Here, we provide new evidence that rapamycin selectively expands the murine naturally occurring CD4(+)CD25(+)FoxP3(+) Tr cells in vitro. These expanded Tr cells suppress proliferation of syngeneic T cells in vitro and prevent allograft rejection in vivo. Interestingly, rapamycin does not block activation-induced cell death and proliferation of CD4(+) T cells in vitro. Based on this new mode of action, rapamycin can be used to expand CD4(+)CD25(+)FoxP3(+) Tr cells for ex vivo cellular therapy in T-cell-mediated diseases. (c) 2005 by The American Society of Hematology.
引用
收藏
页码:4743 / 4748
页数:6
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