Morel Penelope A
Department of Immunology, University of Pittsburgh , Pittsburgh, PA , USA.
Front Immunol. 2013 Dec 6;4:415. doi: 10.3389/fimmu.2013.00415.
Type 1 diabetes (T1D) is a T cell mediated autoimmune disease characterized by immune mediated destruction of the insulin-producing β cells in the islets of Langerhans. Dendritic cells (DC) have been implicated in the pathogenesis of T1D and are also used as immunotherapeutic agents. Plasmacytoid (p)DC have been shown to have both protective and pathogenic effects and a newly described merocytic DC population has been shown to break tolerance in the mouse model of T1D, the non-obese diabetic (NOD) mouse. We have used DC populations to prevent the onset of T1D in NOD mice and clinical trials of DC therapy in T1D diabetes have been initiated. In this review we will critically examine the recent published literature on the role of DC subsets in the induction and regulation of the autoimmune response in T1D.
1型糖尿病(T1D)是一种由T细胞介导的自身免疫性疾病,其特征是免疫介导的胰岛中产生胰岛素的β细胞被破坏。树突状细胞(DC)与T1D的发病机制有关,也被用作免疫治疗剂。浆细胞样(p)DC已被证明具有保护和致病作用,并且新描述的微细胞DC群体已被证明在T1D的小鼠模型即非肥胖糖尿病(NOD)小鼠中会破坏耐受性。我们已使用DC群体来预防NOD小鼠中T1D的发作,并且已经启动了T1D糖尿病的DC治疗临床试验。在这篇综述中,我们将批判性地审视最近发表的关于DC亚群在T1D自身免疫反应的诱导和调节中的作用的文献。