Gut flora antigens are not important in the maintenance of regulatory T cell heterogeneity and homeostasis

被引:53
作者
Min, Booki
Thornton, Angela
Caucheteux, Stephan M.
Younes, Souheil-Antoine
Oh, Keunhee
Hu-Li, Jane
Paul, William E.
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Immunol NB30, Cleveland, OH 44195 USA
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
BrdU; dynamics; germ-free; homeostasis; regulatory T cells;
D O I
10.1002/eji.200737236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD25(+) regulatory T cells (Treg) are a heterogeneous population that exists as CD44(low) and CD44(high) cells. Here we report that while both CD44(low) and CD44(high) Treg are anergic and express similar levels of Foxp3, CD44(high) Treg are highly proliferative in vivo and are more potent suppressors in vitro than CD44(low) Treg. From analysis of the properties of Treg derived from germ-free mice, it was concluded that peptide antigens derived from intestinal microorganisms are not essential for the generation, in vivo proliferation or suppressive activity of Treg. Our results suggest that gut flora antigens play little or no role in the heterogeneity and homeostatic regulation of Treg.
引用
收藏
页码:1916 / 1923
页数:8
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