Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Translational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA, USA.
Curr Diab Rep. 2019 Mar 19;19(5):20. doi: 10.1007/s11892-019-1141-6.
To highlight pathways important for the development of autoimmune diabetes by investigating shared mechanisms of disease in polygenic and monogenic diabetes.
Genome-wide association studies have identified 57 genetic risk loci for type 1 diabetes. Progress has been made in unravelling the mechanistic effects of some of these variants, providing key insights into the pathogenesis of type 1 diabetes. Seven monogenic disorders have also been described where diabetes features as part of an autoimmune syndrome. Studying these genes in relation to polygenic risk loci provides a unique opportunity to dissect pathways important for the development of immune-mediated diabetes. Monogenic autoimmune diabetes can result from the dysregulation of multiple pathways suggesting that small effects on many immune processes are required to drive the autoimmune attack on pancreatic beta cells in polygenic type 1 diabetes. A breakdown in central and peripheral immune tolerance is a common theme in the genetic mechanisms of both monogenic and polygenic disease which highlights the importance of these checkpoints in the development and treatment of islet autoimmunity.
通过研究多基因和单基因糖尿病的共同疾病机制,强调自身免疫性糖尿病发展的重要途径。
全基因组关联研究已经确定了 57 个 1 型糖尿病的遗传风险位点。在揭示其中一些变异的机制影响方面已经取得了进展,为 1 型糖尿病的发病机制提供了重要的见解。也已经描述了七种单基因疾病,其中糖尿病是自身免疫综合征的一部分特征。研究这些基因与多基因风险位点的关系提供了一个独特的机会来剖析对免疫介导的糖尿病发展重要的途径。单基因自身免疫性糖尿病可能是由于多个途径的失调导致的,这表明在多基因 1 型糖尿病中,驱动针对胰腺β细胞的自身免疫攻击需要许多免疫过程的微小影响。中枢和外周免疫耐受的崩溃是单基因和多基因疾病遗传机制的共同主题,这凸显了这些检查点在胰岛自身免疫的发展和治疗中的重要性。