共 40 条
A model of suppression of the antigen-specific CD4 T cell response by regulatory CD25+CD4 T cells in vivo
被引:5
作者:

Thorstenson, KM
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机构: Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA

Herzovi, L
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h-index: 0
机构: Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA

Khoruts, A
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h-index: 0
机构: Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
机构:
[1] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
关键词:
cellular differentiation;
T lymphocytes;
tolerance/suppression/anergy;
transgenic/knockout;
D O I:
10.1093/intimm/dxh213
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Despite intense recent interest, the suppressive mechanisms of regulatory CD25+CD4 T cells remain poorly understood. One deficiency in the field is the lack of in vivo models where the effects of regulatory CD25+CD4 T cells on antigen-specific responder T cells can be measured quantitatively. We describe one such model here. We compared responses of adoptively transferred naive wild-type antigen-specific CD4 T cells in syngeneic CD28-/- and wild-type recipient mice toward a nominal antigen. The cells exhibited a greater degree of proliferation and differentiation in CD28-/- mice and could not be rendered functionally hyporesponsive by systemic exposure to adjuvant-free antigen. The only reason we were able to find to explain this difference was the deficiency of regulatory CD25+CD4 T cells in the CD28-/- mice. Use of CD28-/- mice as adoptive transfer recipients provides a simple model that reveals the contribution of regulatory CD25+CD4 T cells in controlling antigen-driven responses in vivo.
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页码:335 / 342
页数:8
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