Regulatory CD4+ T Cells Promote B Cell Anergy in Murine Lupus

被引:22
|
作者
Liu, Yaoyang [1 ]
Liu, Aijing [1 ,2 ]
Iikuni, Noriko [1 ]
Xu, Huji [3 ]
Shi, Fu-Dong [4 ]
La Cava, Antonio [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Rheumatol, Los Angeles, CA 90095 USA
[2] Hebei Med Univ, Hosp 2, Shijiazhuang 050000, Peoples R China
[3] Second Mil Med Univ, Changzheng Hosp, Shanghai 200433, Peoples R China
[4] St Josephs Hosp, Barrow Neurol Inst, Dept Neurol, Phoenix, AZ 85013 USA
来源
JOURNAL OF IMMUNOLOGY | 2014年 / 192卷 / 09期
关键词
RHEUMATOID-ARTHRITIS; CUTTING EDGE; ERYTHEMATOSUS; PROLIFERATION; LYMPHOCYTES; ACTIVATION; TOLERANCE; DNA; DIFFERENTIATION;
D O I
10.4049/jimmunol.1302897
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 Chi NZW) F-1 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.
引用
收藏
页码:4069 / 4073
页数:5
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