The role of regulatory T cells in the biology of greaft versus host disease

被引:100
作者
Beres, Amy J. [1 ]
Drobyski, William R. [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Microbiol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
关键词
graft versus host disease; regulatory T cells; allogeneic stem cell transplantation; induced regulatory T cells; mouse models; BONE-MARROW-TRANSPLANTATION; TGF-BETA; EX-VIVO; REDUCED FREQUENCY; FOXP3; EXPRESSION; DOWN-REGULATION; SELF-TOLERANCE; NTREG CELLS; LOW-RISK; IN-VIVO;
D O I
10.3389/fimmu.2013.00163
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Graft versus host disease (GVHD) is the major complication of allogeneic hematopoietic stem cell transplantation. GVHD is characterized by an imbalance between the effector and regulatory arms of the immune system which results in the over production of inflammatory cytokines. Moreover, there is a persistent reduction in the number of regulatory T (Treg) cells which limits the ability of the immune system to re-calibrate this proinflammatory environment. Treg cells are comprised of both natural and induced populations which have unique ontological and developmental characteristics that impact how they function within the context of immune regulation. In this review, we summarize pre-clinical data derived from experimental murine models that have examined the role of both natural and induced Treg cells in the biology of GVHD. We also review the clinical studies which have begun to employ Treg cells as a form of adoptive cellular therapy for the prevention of GVHD in human transplant recipients.
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页数:9
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