Doniach D, Bottazzo G F, Cudworth A G
Annu Rev Med. 1983;34:13-20. doi: 10.1146/annurev.me.34.020183.000305.
Type I diabetes is a heterogeneous disorder and the causes of pancreatic beta-cell destruction are unknown. In 1-2% of all cases, viruses (e.g. coxsackie, rubella, mumps, or beta-cell poisons) have been implicated. Twin studies suggest at most 50% of genetic predisposition. In this review we describe the autoimmune components which, in association with inheritance of HLA-haplotypes in susceptible families, allow the future selection of predisposed sibs for possible preventive therapy to retard loss of insulin secretion. The known association of the endocrine autoimmune organ-specific disorders in 10% of Type I diabetics is the extreme expression of the other main genetic ingredient in the development of insulitis in this disease, irrespective of the triggering environmental components. In this "polyendocrine" subgroup and in the "juvenile-onset" cases there is a prolonged latency period during which pancreatic autoimmunity markers are present before clinical expression of the disease.
1型糖尿病是一种异质性疾病,胰腺β细胞破坏的原因尚不清楚。在所有病例中,1% - 2%的病因与病毒(如柯萨奇病毒、风疹病毒、腮腺炎病毒或β细胞毒素)有关。双胞胎研究表明,遗传易感性最多占50%。在本综述中,我们描述了自身免疫成分,这些成分与易感家族中HLA单倍型的遗传相关,使得未来有可能对易感同胞进行选择,以便采取预防性治疗来延缓胰岛素分泌的丧失。在10%的1型糖尿病患者中,已知的内分泌自身免疫性器官特异性疾病关联是该疾病胰岛炎发展中另一个主要遗传成分的极端表现,而与触发疾病的环境因素无关。在这个“多内分泌”亚组和“青少年发病”病例中,有一个较长的潜伏期,在此期间,在疾病临床表现之前就存在胰腺自身免疫标志物。