Cutting edge:: IL-4-induced protection of CD4+CD25- Th cells from CD4+CD25+ regulatory T cell-mediated suppression

被引:53
作者
Pace, Luigia
Rizzo, Stefania
Palombi, Cecilia
Brombacher, Frank
Doria, Gino
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[2] Univ Cape Town, Fac Hlth Sci, Div Immunol, ZA-7700 Rondebosch, South Africa
[3] Univ Cape Town, Fac Hlth Sci, Inst Infect Dis & Mol Med, ZA-7700 Rondebosch, South Africa
关键词
D O I
10.4049/jimmunol.176.7.3900
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) CD25(+) T regulatory (Treg) cells are a CD4+ T cell subset involved in the control of the immune response. In vitro, murine CD4(+) CD25(+) Treg cells inhibit CD4(+) CD25(-) Th cell proliferation induced by anti-CD3 mAb in the presence of APCs. The addition of IL-4 to cocultured cells inhibits CD4(+) CD25(+) Treg cell-mediated suppression. Since all cell types used in the coculture express the IL-4R alpha chain, we used different combinations of CD4(+) CD25(-) Th cells, CD4(+) CD25(+) Treg cells, and APCs from wild-type IL-4R alpha(+/+) or knockout IL-4R alpha(-/-) mice. Results show that the engagement of the IL-4R alpha chain on CD4(+) CD25(-) Th cells renders these cells resistant to suppression. Moreover, the addition of IL-4 promotes proliferation of IL-4R alpha(+/+) CD4(+) CD25(+) Treg cells, which preserve full suppressive competence. These findings support an essential role of IL-4 signaling for CD4(+) CD25(-) Th cell activation and indicate that IL-4-induced proliferation of CD4(+) CD25(+) Treg cells is compatible with their suppressive activity.
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收藏
页码:3900 / 3904
页数:5
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