小胶质细胞
实验性自身免疫性脑脊髓炎
FOXP3型
细胞生物学
过继性细胞移植
免疫学
免疫系统
生物
T细胞
MHC II级
效应器
调节性T细胞
主要组织相容性复合体
炎症
白细胞介素2受体
作者
Friederike Ebner,Christine Brandt,Peggy Thiele,Daniel Richter,Ulrike Schliesser,Volker Siffrin,Jutta Schueler,Tobias Stubbe,Agnes Ellinghaus,Christian Meisel,Birgit Sawitzki,Robert Nitsch
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2013-12-01
卷期号:191 (11): 5594-5602
被引量:67
标识
DOI:10.4049/jimmunol.1203331
摘要
Abstract Although mechanisms leading to brain-specific inflammation and T cell activation have been widely investigated, regulatory mechanisms of local innate immune cells in the brain are only poorly understood. In this study, to our knowledge we show for the first time that MHC class II+CD40dimCD86dimIL-10+ microglia are potent inducers of Ag-specific CD4+Foxp3+ regulatory T cells (Tregs) in vitro. Microglia differentially regulated MHC class II expression, costimulatory molecules, and IL-10 depending on the amount of IFN-γ challenge and Ag dose, promoting either effector T cell or Treg induction. Microglia-induced Tregs were functionally active in vitro by inhibiting Ag-specific proliferation of effector T cells, and in vivo by attenuating experimental autoimmune encephalomyelitis disease course after adoptive transfer. These results indicate that MHC class II+CD40dimCD86dimIL-10+ microglia have regulatory properties potentially influencing local immune responses in the CNS.
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