Autoreactive CD4+ T cells protect from autoimmune diabetes via bystander suppression using the IL-4/stat6 pathway

被引:148
作者
Homann, D
Holz, A
Bot, A
Coon, B
Wolfe, T
Petersen, J
Dyrberg, TP
Grusby, MJ
von Herrath, MG
机构
[1] Scripps Res Inst, Div Virol, Dept Neuropharmacol, La Jolla, CA 92037 USA
[2] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[3] Harvard Univ, Sch Med, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Harvard Sch Publ Hlth, Dept Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S1074-7613(00)80121-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Targeted immune regulation can be achieved by use of tissue-specific T cells and offers the potential for organ-specific suppression of destructive autoimmune processes. Here, we report the generation and characterization of insulin B chain-specific "autoreactive" CD4(+) regulatory T cells that locally suppress diabetogenic T cell responses against an unrelated self-antigen (viral transgene) in a virus-induced model for type 1 diabetes. Interleukin 4 (IL-4) is essential for prevention of diabetes since regulatory T cells cannot be induced in the absence of IL-4 or stat6 (IL-4 signaling pathway). Our observations demonstrate that autoreactive regulatory T cells can suppress autoreactive destructive T cell activity of differential antigenic specificity locally in the pancreatic draining lymph node, probably via cytokine-mediated modulation of antigen-presenting cells.
引用
收藏
页码:463 / 472
页数:10
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