Identification of Circulating Human Antigen-Reactive CD4+ FOXP3+ Natural Regulatory T Cells

被引:31
作者
Litjens, Nicolle H. R. [1 ]
Boer, Karin [1 ]
Betjes, Michiel G. H. [1 ]
机构
[1] Erasmus MC, Div Nephrol & Transplantat, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
关键词
IL-2;
D O I
10.4049/jimmunol.1101974
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Circulating human CD4(+)CD25(++)CD127(-)FOXP3(+) T cells with a persistent demethylated regulatory T cell (Treg)-specific demethylated region Foxp3 gene are considered natural Tregs (nTregs). We have shown that it is possible to identify functional Ag-reactive nTregs cells for a range of different common viral and vaccination Ags. The frequency of these Ag-reactive nTregs within the nTreg population is strikingly similar to the frequency of Ag-reactive T effector cells within the CD4(+) T cell population. The Ag-reactive nTregs could be recognized with great specificity by induction of CD154 expression. These CD154(+) Ag-reactive nTregs showed a memory phenotype and shared all phenotypical and functional characteristics of nTregs. The isolated CD154(+) nTregs could be most efficiently expanded by specific antigenic stimulation, while their Ag-reactive suppressive activity was maintained. After an in vivo booster Ag challenge, the ratio of Ag-reactive T cells to Ag-reactive Tregs increased substantially, which could be attributed to the rise in effector T cells but not Tregs. In conclusion, the nTreg population mirrors the effector T cell population in the frequency of Ag-reactive T cells. Isolation and expansion of functional Ag-reactive nTregs is possible and of potential benefit for specific therapeutic goals. The Journal of Immunology, 2012, 188: 1083-1090.
引用
收藏
页码:1083 / 1090
页数:8
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