Cytotoxic T lymphocyte antigen-4-dependent down-modulation of costimulatory molecules on dendritic cells in CD4+ CD25+ regulatory T-cell-mediated suppression

被引:253
作者
Oderup, Cecilia
Cederbom, Lukas
Makowska, Anna
Cilio, Corrado M.
Ivars, Fredrik
机构
[1] Lund Univ, Immunol Unit, Dept Expt Med Res, SE-22184 Lund, Sweden
[2] Lund Univ, Malmo Univ Hosp, Cellular Autoimmun Unit, Dept Clin Sci, Malmo, Sweden
关键词
co-stimulation/costimulatory molecule; dendritic cells; regulatory T cells;
D O I
10.1111/j.1365-2567.2006.02362.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously demonstrated that CD4(+) CD25(+) natural regulatory T cells (Treg cells) induce down-modulation of CD80 and CD86 (B7) molecules on dendritic cells (DCs) in vitro. In this report we show that the extent of down-modulation is functionally significant because Treg-cell conditioned DCs induced poor T-cell proliferation responses. Further, we report that down-modulation was induced rapidly and was inhibited by blocking cytotoxic T lymphocyte antigen-4 (CTLA-4), which is constitutively expressed by the Treg cells. Even though Treg cells have previously been reported to kill antigen-presenting cells, the down-modulation was not due to selective killing of DCs expressing high level of the costimulatory molecules. We propose that Treg cells down-modulate B7-molecules on DCs in a CTLA-4-dependent way, thereby enhancing suppression of T-cell activity.
引用
收藏
页码:240 / 249
页数:10
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