Maurice Morillon Y, Martin Aaron, Gojanovich Gregory, Wang Bo, Tisch Roland
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC, 27599, USA.
Arch Immunol Ther Exp (Warsz). 2015 Aug;63(4):239-50. doi: 10.1007/s00005-015-0336-z. Epub 2015 Mar 20.
Type 1 diabetes (T1D) is an autoimmune disease in which the insulin-producing β cells are selectively destroyed. β cell-specific T cells are considered to be the major mediators of pathology. Accordingly, most immunotherapies tested in the clinic to date have focused on reestablishing self-tolerance within the T cell compartment. Monoclonal antibodies (Ab) targeting a variety of lymphocyte surface proteins have demonstrated benefits in preclinical and clinical settings. Indeed, the use of Ab to target T cells directly or indirectly has proven to be an effective strategy to rapidly suppress β cell autoimmunity and establish tissue-specific, long-term tolerance in rodent T1D models. In this review, we describe a number of these Ab-based immunotherapies, discuss associated immune regulatory mechanisms, and highlight results obtained in T1D clinical trials.
1型糖尿病(T1D)是一种自身免疫性疾病,其中产生胰岛素的β细胞被选择性破坏。β细胞特异性T细胞被认为是病理过程的主要介质。因此,迄今为止在临床上测试的大多数免疫疗法都集中在重建T细胞区室的自身耐受性上。靶向多种淋巴细胞表面蛋白的单克隆抗体(Ab)在临床前和临床环境中已显示出益处。事实上,使用Ab直接或间接靶向T细胞已被证明是一种有效的策略,可在啮齿动物T1D模型中快速抑制β细胞自身免疫并建立组织特异性的长期耐受性。在这篇综述中,我们描述了一些基于Ab的免疫疗法,讨论了相关的免疫调节机制,并强调了在T1D临床试验中获得的结果。