Kleindienst Petra, Wiethe Carsten, Lutz Manfred B, Brocker Thomas
Institute for Immunology, Ludwig-Maximilians-Universität München, Munich, Germany.
J Immunol. 2005 Apr 1;174(7):3941-7. doi: 10.4049/jimmunol.174.7.3941.
Previous studies suggested that depending on their maturation state, dendritic cells (DC) could either induce T cell tolerance (immature and semimature DC) or T cell activation (mature DC). Pretreatment of C57BL/6 mice with encephalitogenic myelin oligodendrocyte glycoprotein (MOG)(35-55) peptide-loaded semimature DC protected from MOG-induced autoimmune encephalomyelitis. This protection was mediated by IL-10-producing CD4 T cells specific for the self Ag. Here we show that semimature DC loaded with the MHC class II-restricted nonself peptide Ag (OVA) induce an identical regulatory T cell cytokine pattern. However, semimature DC loaded simultaneously with MHC class II- and MHC class I-restricted peptides, could efficiently initiate CD8 T cell responses leading to autoimmune diabetes in a TCR-transgenic adoptive transfer model. Double-peptide-loaded semimature DC also induced simultaneously in the same animal partially activated CD8 T cells with cytolytic function as well as protection from MOG-induced autoimmune encephalomyelitis. Our study suggests that the decision between tolerance and immunity not only depends on the DC, but also on the type and activation requirements of the responding T cell.
先前的研究表明,根据其成熟状态,树突状细胞(DC)既可以诱导T细胞耐受(未成熟和半成熟DC),也可以诱导T细胞活化(成熟DC)。用致脑炎的髓鞘少突胶质细胞糖蛋白(MOG)(35-55)肽负载的半成熟DC预处理C57BL/6小鼠,可预防MOG诱导的自身免疫性脑脊髓炎。这种保护作用是由针对自身抗原产生IL-10的CD4 T细胞介导的。在此我们表明,负载有MHC II类限制性非自身肽抗原(OVA)的半成熟DC诱导相同的调节性T细胞细胞因子模式。然而,在TCR转基因过继转移模型中,同时负载MHC II类和MHC I类限制性肽的半成熟DC可有效启动CD8 T细胞反应,导致自身免疫性糖尿病。负载双肽的半成熟DC还在同一动物中同时诱导具有细胞溶解功能的部分活化CD8 T细胞以及预防MOG诱导的自身免疫性脑脊髓炎。我们的研究表明,耐受与免疫之间的抉择不仅取决于DC,还取决于应答T细胞的类型和活化要求。