CD25+Foxp3+ regulatory T cells facilitate CD4+ T cell clonal anergy induction during the recovery from lymphopenia

被引:20
|
作者
Vanasek, Tracy L.
Nandiwada, Sarada L.
Jenkins, Marc K.
Mueller, Daniel L.
机构
[1] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
来源
JOURNAL OF IMMUNOLOGY | 2006年 / 176卷 / 10期
关键词
D O I
10.4049/jimmunol.176.10.5880
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell clonal anergy induction in lymphopenic nu/nu mice was found to be ineffective. Exposure to a tolerizing peptide Ag regimen instead induced aggressive CD4(+) cell cycle progression and increased Ag responsiveness (priming). Reconstitution of T cell-deficient mice by an adoptive transfer of mature peripheral lymphocytes was accompanied by the development of a CD25(+)Foxp3(+)CTLA-4(+)CD4(+) regulatory T cell population that acted to dampen Ag-driven cell cycle progression and facilitate the induction of clonal anergy in nearby responder CD25(-)CD4(+) T cells. Thus, an early recovery of CD25(+) regulatory T cells following a lymphopenic event can prevent exuberant Ag-stimulated CD4(+) cell cycle progression and promote the development of clonal anergy.
引用
收藏
页码:5880 / 5889
页数:10
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