Adoptive regulatory T cell therapy: challenges in clinical transplantation

被引:34
作者
Safinia, Niloufar [1 ]
Sagoo, Pervinder [1 ]
Lechler, Robert [1 ]
Lombardi, Giovanna [1 ]
机构
[1] Kings Coll London, Med Res Council, Ctr Transplantat, Immunoregulat Lab,Guys Hosp, London SE1 9RT, England
关键词
cellular therapy; clinical transplantation; immune tolerance; regulatory T cells; VERSUS-HOST-DISEASE; TRANSLATIONAL MINIREVIEW SERIES; IMMUNOLOGICAL SELF-TOLERANCE; IN-VITRO GENERATION; CUTTING EDGE; EX-VIVO; INDIRECT ALLOSPECIFICITY; ALLOGRAFT SURVIVAL; TH17; CELLS; COSTIMULATORY BLOCKADE;
D O I
10.1097/MOT.0b013e32833bfadc
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of review The identification and characterisation of regulatory T cells (Tregs) has recently opened up exciting opportunities for Treg cell therapy in transplantation. In this review, we outline the basic biology of Tregs and discuss recent advances and challenges for the identification, isolation and expansion of these cells for cell therapy. Recent findings Tregs of thymic origin have been shown to be key regulators of immune responses in mice and humans, preventing autoimmunity, graft-versus-host disease and organ graft rejection in the transplantation setting. To date, a variety of different methods to isolate and expand Tregs ex vivo have been advocated. Although promising, relatively few clinical trials of human Treg cell infusion have been initiated. Summary Many key questions about Treg cell therapy still remain and here we provide an in-depth analysis and highlight the challenges and opportunities for immune intervention with Treg-based therapeutics in clinical transplantation.
引用
收藏
页码:427 / 434
页数:8
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