Department of Dermatology, University Clinics, Ludwig-Maximilian-University of Munich, Munich, Germany.
Autoimmun Rev. 2017 Sep;16(9):970-979. doi: 10.1016/j.autrev.2017.07.011. Epub 2017 Jul 10.
Chronic immune-mediated disorders (IMDs) constitute a major health burden. Understanding IMD pathogenesis is facing two major constraints: Missing heritability explaining familial clustering, and missing autoantigens. Pinpointing IMD risk genes and autoimmune targets, however, is of fundamental importance for developing novel causal therapies. The strongest association of all IMDs is seen with human leukocyte antigen (HLA) alleles. Using psoriasis as an IMD model this article reviews the pathogenic role HLA molecules may have within the polygenic predisposition of IMDs. It concludes that disease-associated HLA alleles account for both missing heritability and autoimmune mechanisms by facilitating tissue-specific autoimmune responses through autoantigen presentation.
慢性免疫介导性疾病(IMD)是一个主要的健康负担。了解 IMD 的发病机制面临两个主要的限制:解释家族聚集的遗传缺失和自身抗原的缺失。然而,确定 IMD 的风险基因和自身免疫靶标对于开发新的因果治疗方法至关重要。在所有 IMD 中,与人类白细胞抗原(HLA)等位基因的关联最强。本文以银屑病为 IMD 模型,综述了 HLA 分子在 IMD 多基因易感性中的致病作用。它得出结论,疾病相关的 HLA 等位基因通过自身抗原呈递促进组织特异性自身免疫反应,从而解释了遗传缺失和自身免疫机制。