Regulation of antigen-expressing dendritic cells by double negative regulatory T cells

被引:44
作者
Gao, Julia Fang [1 ,2 ]
McIntyre, Megan S. Ford [1 ]
Juvet, Stephen C. [1 ]
Diao, Jun [1 ]
Li, Xujian [1 ]
Vanama, Ramesh B. [1 ]
Mak, Tak W. [2 ,3 ]
Cattral, Mark S. [1 ]
Zhang, Li [1 ,2 ]
机构
[1] Univ Toronto, Transplant Inst, Toronto Gen Res Inst, Univ Hlth Network, Toronto, ON, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[3] Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
关键词
CTLA4; DCs; Double negative regulatory T cells; Fas-FasL pathway; CARDIAC XENOGRAFT SURVIVAL; GRAFT-VERSUS-HOST; IN-VIVO; DEPENDENT ELIMINATION; MICE; SUPPRESSION; TOLERANCE; INFUSION; VITRO; TRANSPLANTATION;
D O I
10.1002/eji.201141428
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TCR alpha beta(+)CD3(+)CD4 CD8 NK1.1 double negative (DN) Tregs comprise 1-3% of peripheral T lymphocytes in mice and humans. It has been demonstrated that DN Tregs can suppress allo-, xeno- and auto-immune responses in an Ag-specific fashion. However, the mechanisms by which DN Tregs regulate immune responses remain elusive. Whether DN Tregs can regulate DCs has not been investigated previously. In this study, we demonstrate that DN Tregs express a high level of CTLA4 and are able to down-regulate costimulatory molecules CD80 and CD86 expressed on Ag-expressing mature DCs (mDCs). DN Tregs from CTLA4 KO mice were not able to downregulate CD80 and CD86 expression, indicating that CTLA4 is critical for DN Treg-mediated downregulation of costimulatory molecule expression on Ag-expressing mature DCs. Furthermore, DN Tregs could kill both immature and mature allogeneic DCs, as well as Ag-loaded syngeneic DCs, in an Ag-specific manner in vitro and in vivo, mainly through the Fas-FasL pathway. These data demonstrate, for the first time, that DN Tregs are potent regulators of DCs and may have the potential to be developed as a novel immune suppression treatment.
引用
收藏
页码:2699 / 2708
页数:10
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