Agarwal K, Jones D E, Bassendine M F
Centre for Liver Research, University of Newcastle, Newcastle Upon Tyne, UK.
Eur J Gastroenterol Hepatol. 1999 Jun;11(6):603-6. doi: 10.1097/00042737-199906000-00004.
Family studies suggest that genetic factors play a role in determining susceptibility to primary biliary cirrhosis (PBC). A number of polymorphic genes with small and additive effects may thus encode factors predisposing to this 'polygenic' disease. All the published data on genetic predisposition to PBC have been obtained from association studies, based on comparison of the frequency of an allele in unrelated affected and unaffected individuals from a population; however, many studies have examined only small datasets. There is evidence from several different populations to support a role for the major histocompatibility complex (MHC) class II antigen, HLA DR8, in increased risk of PBC. Other 'candidate' genes, selected on the basis of postulated mechanisms of breakdown of self-tolerance, are now beginning to be tested in association studies, including cytokines and immunomodulatory molecules. These studies and other approaches to identifying genes that confer susceptibility to an autoimmune disorder, exemplified by PBC, are discussed.
家族研究表明,遗传因素在决定原发性胆汁性肝硬化(PBC)的易感性方面发挥作用。因此,一些具有微小累加效应的多态性基因可能编码导致这种“多基因”疾病的因素。所有已发表的关于PBC遗传易感性的数据均来自关联研究,该研究基于比较人群中无关患病个体和未患病个体的等位基因频率;然而,许多研究仅检测了小数据集。来自几个不同人群的证据支持主要组织相容性复合体(MHC)II类抗原HLA DR8在增加PBC风险中发挥作用。其他基于自身耐受破坏的假定机制选择的“候选”基因,目前正开始在关联研究中进行检测,包括细胞因子和免疫调节分子。本文讨论了这些研究以及其他识别导致自身免疫性疾病(如PBC)易感性基因的方法。