Visualizing regulatory T cell control of autoimmune responses in nonobese diabetic mice

被引:0
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作者
Qizhi Tang
Jason Y Adams
Aaron J Tooley
Mingying Bi
Brian T Fife
Pau Serra
Pere Santamaria
Richard M Locksley
Matthew F Krummel
Jeffrey A Bluestone
机构
[1] University of California,Department of Medicine
[2] San Francisco,Department of Pathology
[3] Diabetes Center,Howard Hughes Medical Institute and Department of Medicine
[4] University of California,Julia McFarlane Diabetes Research Centre and Department of Microbiology & Infectious Diseases
[5] University of California,undefined
[6] University of California,undefined
[7] University of Calgary,undefined
来源
Nature Immunology | 2006年 / 7卷
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摘要
The in vivo mechanism of regulatory T cell (Treg cell) function in controlling autoimmunity remains controversial. Here we have used two-photon laser-scanning microscopy to analyze lymph node priming of diabetogenic T cells and to delineate the mechanisms of Treg cell control of autoimmunity in vivo. Islet antigen–specific CD4+CD25− T helper cells (TH cells) and Treg cells swarmed and arrested in the presence of autoantigens. These TH cell activities were progressively inhibited in the presence of increasing numbers of Treg cells. There were no detectable stable associations between Treg and TH cells during active suppression. In contrast, Treg cells directly interacted with dendritic cells bearing islet antigen. Such persistent Treg cell–dendritic cell contacts preceded the inhibition of TH cell activation by dendritic cells, supporting the idea that dendritic cells are central to Treg cell function in vivo.
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页码:83 / 92
页数:9
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