In vitro expanded alloantigen-specific CD4+CD25+ regulatory T cell treatment for the induction of donor-specific transplantation tolerance

被引:16
|
作者
Jiang, Shuiping [1 ]
Golshayan, Dela [1 ]
Tsang, Julia [1 ]
Lombardi, Giovanna [1 ]
Lechler, Robert I. [1 ]
机构
[1] Kings Coll London, Guys Hosp, Dept Nephrol & Transplantat, London SE1 9RT, England
关键词
CD4(+)CD25(+) T cells; FoxP3; regulatory T cells; adoptive cell therapy; indirect allospecificity; transplantation tolerance;
D O I
10.1016/j.intimp.2006.07.025
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 key goal in clinical transplantation is the induction of donor-specific transplantation tolerance to minimise the morbidity and mortality associated with long-term immunosuppression. Naturally occurring CD4(+)CD25(+) regulatory T cells (Tregs) expressing forkhead transcript factor FoxP3 play a Crucial role in the prevention of autoimmunity, and appear to mediate transplantation tolerance, and these cells can have indirect allospecificity for donor antigens. Here we show that self-reactive human CD4(+)CD25(+) Tregs can be Subverted into allopeptide-specific cells in vitro and be expanded to large cell numbers, and that similar in vitro expanded murine CD4(+)CD25(+) Tregs with indirect allospecificity were capable of inducing donor-specific experimental transplantation tolerance. These data provide a platform for clinical studies using CD4(+)CD25(+) Tregs with indirect allospecificity as potential reagents for the induction of donor-specific transplantation tolerance. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1879 / 1882
页数:4
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