Regulatory CD4+ T Cells Promote B Cell Anergy in Murine Lupus
Author(s) -
Yaoyang Liu,
Aijing Liu,
Noriko Iikuni,
Huji Xu,
FuDong Shi,
Antonio La Cava
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1302897
Subject(s) - immunology , foxp3 , autoantibody , systemic lupus erythematosus , autoimmunity , b cell , il 2 receptor , biology , t cell , medicine , immune system , antibody , disease
To prevent autoimmunity, anergy of autoreactive B cells needs to be maintained, together with the suppression of hyperactive B cells. We previously reported that CD4(+)CD25(+)Foxp3(+) regulatory T cells (Tregs) can directly suppress autoantibody-producing autoreactive B cells in systemic lupus erythematosus. In this article, we show that Tregs can also reduce the production of autoantibodies in (NZB × NZW)F1 mouse lupus B cells by promoting B cell anergy, both in vitro and in vivo. This phenomenon associated with a reduction in Ca(2+) flux in B cells, and CTLA-4 blockade inhibited the effects of Tregs on anergic lupus B cells. These findings identify a new mechanism by which Tregs can control production of autoantibodies in lupus B cells and, more generally, B cell activity in physiopathological conditions.
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