作者
Paul A Blair, Karina A Chavez-Rueda, Jamie G Evans, Mark J Shlomchik, Ayad Eddaoudi, David A Isenberg, Michael R Ehrenstein, Claudia Mauri
发表日期
2009/3/15
期刊
The Journal of Immunology
卷号
182
期号
6
页码范围
3492-3502
出版商
American Association of Immunologists
简介
We have previously reported that IL-10+ regulatory B cells, known to play an important role in controlling autoimmunity and inflammatory disorders, are contained within the transitional 2 immature (T2) B cell pool (T2 Bregs). Therapeutic strategies facilitating their enrichment or enhancing their suppressive activity are highly attractive. In this study, we report that agonistic anti-CD40 specifically targets T2 B cells and enriches Bregs upon short-term in vitro culture. Although transfer of unmanipulated T2 B cells, isolated from mice with established lupus, failed to confer protection to diseased mice, transfer of in vitro anti-CD40-generated T2 B cells (T2-like-Bregs) significantly improved renal disease and survival by an IL-10-dependent mechanism. T2-like-Bregs readily accumulated in the spleen after transfer, suppressed Th1 responses, induced the differentiation of IL-10+ CD4+ T cells, and conveyed a regulatory effect …
引用总数
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