Goubier Anne, Dubois Bertrand, Gheit Hanane, Joubert Grégoire, Villard-Truc Florence, Asselin-Paturel Carine, Trinchieri Giorgio, Kaiserlian Dominique
INSERM, U851, 21 Avenue Tony Garnier, Lyon F-69007, France.
Immunity. 2008 Sep 19;29(3):464-75. doi: 10.1016/j.immuni.2008.06.017.
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.
口服耐受可防止对饮食抗原(包括蛋白质和半抗原)的口服致敏以及迟发型超敏反应(DTH)的发生。我们在此表明,浆细胞样树突状细胞(pDCs)可防止口服T细胞致敏,并负责对由抗原喂食诱导的CD4(+)和CD8(+) T细胞介导的DTH反应产生全身耐受性。pDCs的全身耗竭可阻止通过抗原喂食诱导的耐受性。将口服负载抗原的肝脏pDCs转移至未致敏的受体小鼠,分别诱导了对蛋白质和半抗原的CD4(+)和CD8(+) T细胞反应的抗原特异性抑制。肝脏是口服抗原呈递的部位,pDCs似乎通过一种不依赖CD4(+) T细胞的机制,相对迅速地在肝脏中诱导抗原特异性T细胞的无反应性或缺失。这些数据表明,口服耐受依赖于pDC向T细胞呈递抗原,并提示pDC可能是肠道和全身性炎症性疾病的关键治疗靶点。