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Owing to the adverse effects of immunosuppression and an inability to prevent chronic rejection, there is a pressing need for alternative strategies to control alloimmunity. In three decades, regulatory T cells (Tregs) have evolved from a hypothetical mediator of adoptively transferred tolerance to a well-defined population that can be expanded ex vivo and returned safely to patients in clinical trials. Herein, we review the historical developments that have permitted these advances and the current status of clinical trials examining Tregs as a cellular therapy in transplantation. We conclude by discussing the critical unanswered questions that face this field in the coming years. © Copyright 2014 The American Society of Transplantation and the American Society of Transplant Surgeons.

Original publication

DOI

10.1111/ajt.12647

Type

Journal article

Journal

American Journal of Transplantation

Publication Date

01/01/2014

Volume

14

Pages

750 - 763