Powers A C, Eisenbarth G S
Annu Rev Med. 1985;36:533-44. doi: 10.1146/annurev.me.36.020185.002533.
Current evidence indicates that Type I diabetes mellitus is a slowly progressive autoimmune disease resulting in complete beta-cell destruction in genetically susceptible individuals. Histocompatibility region genes are major determinants of genetic susceptibility, and more than 90% of Type I individuals express HLA alleles DR3 or DR4. Prior to clinical diabetes, islet-cell antibodies and activated T lymphocytes are found in conjunction with a slowly progressive loss of intravenous glucose-stimulated insulin secretion. Present clinical research efforts are aimed at detection of susceptible individuals prior to the development of diabetes and selective immunotherapy to halt beta-cell destruction.
目前的证据表明,1型糖尿病是一种缓慢进展的自身免疫性疾病,会导致基因易感性个体的β细胞完全破坏。组织相容性区域基因是遗传易感性的主要决定因素,超过90%的1型个体表达HLA等位基因DR3或DR4。在临床糖尿病出现之前,可发现胰岛细胞抗体和活化的T淋巴细胞,同时伴有静脉注射葡萄糖刺激的胰岛素分泌缓慢进展性丧失。目前的临床研究工作旨在在糖尿病发生之前检测出易感个体,并进行选择性免疫治疗以阻止β细胞破坏。