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人类白细胞抗原II类区域基因与疱疹样皮炎易感性:DPB1和TAP2的关联继发于DQ亚区域的关联。

HLA class II region genes and susceptibility to dermatitis herpetiformis: DPB1 and TAP2 associations are secondary to those of the DQ subregion.

作者信息

Hall M A, Lanchbury J S, Ciclitira P J

机构信息

Molecular Immunogenetics Unit, Division of Medicine, UMDS, Guy's Hospital, London, UK.

出版信息

Eur J Immunogenet. 1996 Aug;23(4):285-96. doi: 10.1111/j.1744-313x.1996.tb00124.x.

Abstract

Classical dermatitis herpetiformis (DH) is associated with similar HLA class I, II and III polymorphisms to coeliac disease (CD). The two diseases share distinctive pathological changes to the small intestinal mucosa which reverse on withdrawal of dietary gluten. In order to determine the locus primarily associated with DH, and to examine whether there is a common genetic link predisposing to the enteropathy seen in both DH and coeliac disease, HLA-DR, DQ and DP subregion associations were investigated by HLA genotyping in 23 DH patients and 64 healthy controls. We also studied polymorphisms of the TAP2 locus, which is located between the DP and DQ subregions. Genotyping was carried out by PCR of genomic DNA with allelic assignment by sequence-specific oligonucleotide (SSO) hybridization or amplification refractory mutation system (ARMS). The strongest associations in the patient group were with HLA DRB10301 (91% vs 22% of controls), HLA DQB102 (100% vs 32% of controls) and DPB10101 (39% and 14%). These associations are similar to those described for CD. 100% of DH patients were positive for the DQA10501/DQB1*02 dimer in cis or trans and, by analogy with CD, this is probably responsible for presenting gliadin peptide implicated in the disease process. Homozygosity for DQ2 was significantly increased in the CD patient group compared to the DH patient group (65% versus 39%), and so differences in dosage of HLA class II genotypes between DH and CD may be responsible for the milder gastrointestinal symptoms characteristic of DH.

摘要

经典型疱疹样皮炎(DH)与乳糜泻(CD)具有相似的HLA Ⅰ类、Ⅱ类和Ⅲ类基因多态性。这两种疾病在小肠黏膜具有独特的病理变化,在去除饮食中的麸质后这些变化会逆转。为了确定与DH主要相关的基因座,并研究是否存在共同的遗传联系导致DH和乳糜泻中出现的肠病,通过对23例DH患者和64例健康对照进行HLA基因分型,研究了HLA - DR、DQ和DP亚区的关联。我们还研究了位于DP和DQ亚区之间的TAP2基因座的多态性。通过对基因组DNA进行PCR,并通过序列特异性寡核苷酸(SSO)杂交或扩增阻滞突变系统(ARMS)进行等位基因分型。患者组中最强的关联是与HLA DRB10301(91%对对照组的22%)、HLA DQB102(100%对对照组的32%)和DPB10101(39%对14%)。这些关联与CD中描述的相似。100%的DH患者DQA10501/DQB1*02二聚体顺式或反式呈阳性,与CD类似,这可能负责呈递与疾病过程相关的麦醇溶蛋白肽。与DH患者组相比,CD患者组中DQ2纯合子显著增加(65%对39%),因此DH和CD之间HLA Ⅱ类基因型剂量的差异可能是DH较轻的胃肠道症状的原因。

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