Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3841156 | Translational Research | 2009 | 11 Pages |
Abstract
CD4+CD25+ T cells were identified originally as potent suppressors of autoimmunity and were later termed “natural regulatory T cells” or nTreg cells. Subsequently, a transcription factor called forkhead box protein 3 (Foxp3) was identified to be a critical regulator for Treg differentiation and function. Foxp3+CD4+CD25+ Treg cells have been increasingly documented to suppress allograft rejection and to mediate allograft tolerance in transplantation. In this article, the authors review current approaches for amplification of allo-specific Foxp3+CD4+CD25+ Treg cells for prevention of allograft rejection and induction of allo-specific transplant tolerance.
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Authors
Guliang Xia, Malathi Shah, Xunrong Luo,