Lieberman S M, DiLorenzo T P
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Tissue Antigens. 2003 Nov;62(5):359-77. doi: 10.1034/j.1399-0039.2003.00152.x.
Type 1 diabetes (T1D) is an organ-specific autoimmune disease in which the insulin-producing beta cells in the pancreatic islets are selectively eliminated. T cells specific for beta-cell antigens are the mediators of this precise cellular destruction. However, antibodies to beta-cell proteins are also generated and may be used for predicting disease in at-risk populations. Over the past two decades, numerous beta-cell proteins and lipids have been implicated as autoantigens in patients or in non-obese diabetic (NOD) mice, a well-studied animal model of T1D. Here, we present a review of these antigens, accompanied by their T-cell epitopes, where known, and a discussion of our current understanding of why particular self-proteins become disease-inciting antigens. Although two dozen beta-cell antigens have been identified to date, few of these have been confirmed to be recognized by pathogenic T cells early in the disease process. Further identification and characterization of initiating beta-cell antigens targeted by pathogenic T cells should be a priority for future studies.
1型糖尿病(T1D)是一种器官特异性自身免疫性疾病,其中胰岛中产生胰岛素的β细胞被选择性清除。针对β细胞抗原的T细胞是这种精确细胞破坏的介质。然而,也会产生针对β细胞蛋白的抗体,这些抗体可用于预测高危人群的疾病。在过去二十年中,许多β细胞蛋白和脂质在患者或非肥胖糖尿病(NOD)小鼠(一种经过充分研究的T1D动物模型)中被认为是自身抗原。在这里,我们对这些抗原及其已知的T细胞表位进行综述,并讨论我们目前对特定自身蛋白为何成为致病抗原的理解。尽管迄今为止已鉴定出二十多种β细胞抗原,但其中很少有被证实能在疾病早期被致病性T细胞识别。进一步鉴定和表征致病性T细胞靶向的起始β细胞抗原应是未来研究的重点。