van Heel David A, Hunt Karen, Greco Luigi, Wijmenga Cisca
Department of Gastroenterology, Imperial College London, Du Cane Road, London W12 0NN, UK.
Best Pract Res Clin Gastroenterol. 2005 Jun;19(3):323-39. doi: 10.1016/j.bpg.2005.01.001.
Coeliac disease has a strong genetic component, higher than for many other common complex diseases. Possession of the HLA-DQ2 variant is required for presentation of disease causing dietary antigens to T cells, although this is also common in the healthy population. Non-HLA genetic factors account for the majority of heritable risk. Linkage studies have identified promising regions on chromosomes 5 and 19, with multiple other loci awaiting definitive confirmation in independent studies. Inherited variants in the tightly clustered chromosome 2q CD28-CTLA4-ICOS region are associated with disease, although of weak effect size. Larger sample sizes are necessary in coeliac disease genetic studies to detect small effects, alternatively meta-analysis offers promise. Newer methods including gene expression analysis and genome wide association studies will advance understanding of genetic susceptibility. Identification of coeliac disease genes may improve diagnostic/prognostic markers, basic understanding of disease aetiology, permit development of novel therapeutics and provide insight into other autoimmune disorders.
乳糜泻具有很强的遗传因素,比许多其他常见的复杂疾病都要高。呈现致病饮食抗原给T细胞需要拥有HLA-DQ2变体,尽管这在健康人群中也很常见。非HLA遗传因素占可遗传风险的大部分。连锁研究已经在5号和19号染色体上确定了有希望的区域,还有多个其他位点有待独立研究的确证。紧密聚集的2q染色体上CD28-CTLA4-ICOS区域的遗传变异与疾病相关,尽管效应大小较弱。在乳糜泻遗传研究中需要更大样本量来检测微小效应,或者荟萃分析有前景。包括基因表达分析和全基因组关联研究在内的更新方法将推进对遗传易感性的理解。乳糜泻基因的鉴定可能会改善诊断/预后标志物,增进对疾病病因的基本理解,允许开发新的治疗方法,并为其他自身免疫性疾病提供见解。