Generation of HSP60-specific regulatory T cell and effect on atherosclerosis

被引:34
作者
Yang, Keping [1 ]
Li, Dazhu [1 ]
Luo, Minghua [1 ]
Hu, Yingfeng [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Cardiol,Inst Cardiovasc Dis, Wuhan 430022, Peoples R China
关键词
regulatory T cell; atherosclerosis; dendritic cell;
D O I
10.1016/j.cellimm.2007.01.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although CD4(+)CD25(+) regulatory T cells are pivotal in the suppression of autoinummity, little is known about the effect of antigen-specific regulatory T cells on the formation of atheromatous plaques. Here, we describe the induction of heat-shock protein 60 (HSP60)-specific CD4(+)CD25(high) T cells by rapamycin (RPM)-treated immature dendritic cells in vitro and explore their effect on plaques in apolipoprotein E-deficient mice. Rapamycin-treated bone marrow-derived dendritic cells (DC) were immature, expressing a low level of co-stimulation factors CD86 and CD80. Naive CD4(+) T cells expressed high levels of CD25 and forkhead box P3 (Foxp3) after incubation with rapamycin-treated and HSP60-loaded DC and displayed moderate antigen-specific, IL-10-independent inhibitory function in vitro. After adoptive transfer, HSP60-specific CD4(+)CD25(high) T cells inhibited the formation of plaques, while ovalbumin-specific cells did not. These findings suggest that RPM-treated DC can induce antigen-specific CD4(+)CD25(high) Treg cells that have inhibitory activity in vitro and prevent the development of plaques in vivo. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:90 / 95
页数:6
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