Enhanced engagement of CTLA-4 induces antigen-specific CD4+CD25+Foxp3+ and CD4+CD25- TGF-β1+ adaptive regulatory T cells

被引:46
作者
Li, Ruobing
Perez, Nicolas
Karumuthil-Melethil, Subha
Prabhakar, Bellur S.
Holterman, Mark J.
Vasu, Chenthamarakshan
机构
[1] Univ Illinois, Dept Surg, Coll Med, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Med, Dept Microbiol & Immunol, Chicago, IL 60612 USA
关键词
D O I
10.4049/jimmunol.179.8.5191
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CTLA-4 is a critical negative regulator of T cell response and is instrumental in maintaining immunological tolerance. In this article, we report that enhanced selective engagement of CTLA-4 on T cells by Ag-presenting dendritic cells resulted in the induction of Ag-specific CD4(+)CD25(+)Foxp3(+) and CD4(+)CD25(-)TGF-beta 1(+) adaptive Tregs. These cells were CD62L(low) and hypo-responsive to stimulation with cognate Ag but demonstrated a superior ability to suppress Ag-specific effector T cell response compared with their CD62L(high) counterparts. Importantly, treatment of mice with autoimmune thyroiditis using mouse thyroglobulin (mTg)-pulsed anti-CTLA-4 agonistic Ab-coated DCs, which results in a dominant engagement of CTLA-4 upon self-Ag presentation, not only suppressed thyroiditis but also prevented reemergence of the disease upon rechallenge with mTg. Further, the disease suppression was associated with significantly reduced mTg-specific T cell and Ab responses. Collectively, our results showed an important role for selective CTLA-4 signaling in the induction of adaptive Tregs and suggested that approaches that allow dominant CTLA-4 engagement concomitant with Ag-specific TCR ligation can be used for targeted therapy.
引用
收藏
页码:5191 / 5203
页数:13
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