Pinkse Gabrielle G M, Boitard Christian, Tree Timothy I M, Peakman Mark, Roep Bart O
Department of Immunohematology and Blood Transfusion, E3Q, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Ann N Y Acad Sci. 2006 Oct;1079:19-23. doi: 10.1196/annals.1375.003.
Islet autoreactive CD8 T cells are plausible candidates for direct beta cell toxicity in type 1 diabetes (T1DM). In 2005, cellular studies in the pathogenesis of this disease have reached a new milestone. Autoreactive CD8 T cells have been defined and several target islet epitopes of these have been discovered and validated simultaneously in three independent studies. The insulin B10-B18 peptide that displays exceptional binding affinity for HLA-A2 has been reported in all three studies, and its recognition shows an association with autoimmune beta cell destruction and T1DM. These studies imply that CD8 T cell-based HLA tetramers and ELISPOT analyses can be useful to monitor T1DM as well as islet transplantation, and may provide useful tools to assess immunological efficacy of immune intervention trials.
胰岛自身反应性CD8 T细胞可能是1型糖尿病(T1DM)中直接导致β细胞毒性的候选因素。2005年,关于该疾病发病机制的细胞研究达到了一个新的里程碑。自身反应性CD8 T细胞已被定义,并且在三项独立研究中同时发现并验证了其中几个胰岛靶抗原表位。在所有三项研究中均报告了对HLA - A2具有特殊结合亲和力的胰岛素B10 - B18肽,对其的识别显示与自身免疫性β细胞破坏和T1DM有关。这些研究表明,基于CD8 T细胞的HLA四聚体和ELISPOT分析可用于监测T1DM以及胰岛移植,并且可能为评估免疫干预试验的免疫疗效提供有用的工具。