CD40 ligation releases immature dendritic cells from the control of regulatory CD4+CD25+ T cells

被引:230
作者
Serra, P
Amrani, A
Yamanouchi, J
Han, BY
Thiessen, S
Utsugi, T
Verdaguer, J
Santamaria, P
机构
[1] Univ Calgary, Julia McFarlane Diabet Res Ctr, Fac Med, Calgary, AB T2N 4N1, Canada
[2] Gunma Univ, Sch Med, Dept Internal Med 2, Gunma 371, Japan
基金
加拿大健康研究院;
关键词
D O I
10.1016/S1074-7613(03)00327-3
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 report that disruption of CD154 in nonobese diabetic (NOD) mice abrogates the helper function of CD4(+)CD25(-) T cells without impairing the regulatory activity of CD4(+)CD25(+) T cells. Whereas CD4(+) T cells from NOD mice enhanced a diabetogenic CD8(+) T cell response in monoclonal TCR-transgenic NOD mice, CD4(+) T cells from NOD.CD154(-/-) mice actively suppressed it. Suppression was mediated by regulatory CD4(+)CD25(+) T cells capable of inhibiting CD8(+) T cell responses induced by peptide-pulsed dendritic cells (DCs), but not peptide/MHC monomers. It involved inhibition of DC maturation, did not occur in the presence of CD154(+) T-helper cells, and could be inhibited by activation of DCs with LPS, CpG DNA, or an agonistic anti-CD40 mAb. Thus, in at least some genetic backgrounds, CD154-CD40 interactions and innate stimuli release immature DCs from suppression by CD4(+)CD25(+) T cells.
引用
收藏
页码:877 / 889
页数:13
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