Cutting edge:: Direct suppression of B cells by CD4+CD25+ regulatory T cells

被引:480
作者
Lim, HW
Hillsamer, P
Banham, HH
Kim, CH
机构
[1] Purdue Univ, Lab Immunol & Hematopoiesis, Dept Pathobiol, W Lafayette, IN 47907 USA
[2] Purdue Univ, Purdue Canc Ctr, W Lafayette, IN 47907 USA
[3] Purdue Univ, Bindley Biosci Ctr, W Lafayette, IN 47907 USA
[4] Purdue Univ, Biochem & Mol Biol Program, W Lafayette, IN 47907 USA
[5] Sagamore Surg Ctr, Lafayette, IN 47909 USA
[6] Univ Oxford, Nuffield Dept Clin Lab Sci, Oxford OX1 2JD, England
关键词
D O I
10.4049/jimmunol.175.7.4180
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Tregs) can potentially migrate to the B cell areas of secondary lymphoid tissues and suppress T cell-dependent B cell Ig response. T cell-dependent Ig response requires B cell stimulation by Th cells. It has been unknown whether Tregs can directly suppress B cells or whether they must suppress Th cells to suppress B cell response. We report here that Foxp3(+) Tregs are found in T-B area borders and within germinal centers of human lymphoid tissues and can directly suppress B cell Ig response. Although Tregs can effectively suppress T cells, they can also directly suppress B cell response without the need to first suppress Th cells. The direct suppression of B cell Ig production by Tregs is accompanied by inhibition of Ig class switch recombination.
引用
收藏
页码:4180 / 4183
页数:4
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