共 45 条
Plasmacytoid dendritic cells mediate oral tolerance
被引:304
作者:

Goubier, Anne
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机构:
INSERM, U851, F-69007 Lyon, France
Univ Lyon 1, IFR128, F-69622 Villeurbanne, France INSERM, U851, F-69007 Lyon, France

Dubois, Bertrand
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h-index: 0
机构:
INSERM, U851, F-69007 Lyon, France
Univ Lyon 1, IFR128, F-69622 Villeurbanne, France INSERM, U851, F-69007 Lyon, France

Gheit, Hanane
论文数: 0 引用数: 0
h-index: 0
机构:
INSERM, U851, F-69007 Lyon, France
Univ Lyon 1, IFR128, F-69622 Villeurbanne, France INSERM, U851, F-69007 Lyon, France

Joubert, Grgoire
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h-index: 0
机构:
INSERM, U851, F-69007 Lyon, France
Univ Lyon 1, IFR128, F-69622 Villeurbanne, France INSERM, U851, F-69007 Lyon, France

Villard-Truc, Florence
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Edouard Herriot, Hosp Civils Lyon, Serv Gastroenterol Pediat, F-69003 Lyon, France INSERM, U851, F-69007 Lyon, France

Asselin-Paturel, Carine
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h-index: 0
机构:
Schering Plough Lab Immunol Res, F-69570 Dardilly, France INSERM, U851, F-69007 Lyon, France

Trinchieri, Giorgio
论文数: 0 引用数: 0
h-index: 0
机构:
Schering Plough Lab Immunol Res, F-69570 Dardilly, France
NCI, Ctr Canc Res, Canc & Inflammat Program, Frederick, MD 21702 USA INSERM, U851, F-69007 Lyon, France

Kaiserlian, Dominique
论文数: 0 引用数: 0
h-index: 0
机构:
INSERM, U851, F-69007 Lyon, France
Univ Lyon 1, IFR128, F-69622 Villeurbanne, France INSERM, U851, F-69007 Lyon, France
机构:
[1] INSERM, U851, F-69007 Lyon, France
[2] Univ Lyon 1, IFR128, F-69622 Villeurbanne, France
[3] Hop Edouard Herriot, Hosp Civils Lyon, Serv Gastroenterol Pediat, F-69003 Lyon, France
[4] Schering Plough Lab Immunol Res, F-69570 Dardilly, France
[5] NCI, Ctr Canc Res, Canc & Inflammat Program, Frederick, MD 21702 USA
来源:
关键词:
D O I:
10.1016/j.immuni.2008.06.017
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Oral tolerance prevents oral sensitization to dietary antigens (Ags), including proteins and haptens, and development of delayed-type hypersensitivity (DTH) responses. We showed here that plasmacytoid dendritic cells (pDCs) prevented oral T cell priming and were responsible for systemic tolerance to CD4(+) and CD8(+) T cell-mediated DTH responses induced by Ag feeding. Systemic depletion of pDCs prevented induction of tolerance by antigen feeding. Transfer of oral Ag-loaded liver pDCs to naive recipient mice induced Ag-specific suppression of CD4(+) and CD8(+) T cell responses to protein and hapten, respectively. Liver is a site of oral Ag presentation, and pDCs appeared to induce anergy or deletion of Ag-specific T cells in the liver relatively rapidly via a CD4(+) T cell-independent mechanism. These data demonstrate that oral tolerance relies on Ag presentation by pDC to T cells and suggest that pDC could represent a key therapeutic target for intestinal and systemic inflammatory diseases.
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页码:464 / 475
页数:12
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