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HLA基因在弥漫性泛细支气管炎遗传易感性中的作用。

Contribution of HLA genes to genetic predisposition in diffuse panbronchiolitis.

作者信息

Keicho N, Tokunaga K, Nakata K, Taguchi Y, Azuma A, Bannai M, Emi M, Ohishi N, Yazaki Y, Kudoh S

机构信息

Third Department of Internal Medicine, University of Tokyo; Department of Human Genetics, Graduate School of Medical Sciences, University of Tokyo, Japan.

出版信息

Am J Respir Crit Care Med. 1998 Sep;158(3):846-50. doi: 10.1164/ajrccm.158.3.9712125.

Abstract

Diffuse panbronchiolitis (DPB) in East Asia is a distinctive chronic obstructive pulmonary disease of unknown etiology. We hypothesize that the disease susceptibility is due to genetic predisposition unique to Asians. Association between human leukocyte antigen (HLA)-Bw54 and the disease was previously reported. In the present study, using newly developed polymerase chain reaction (PCR)- based methods, we directly analyzed HLA class I and II alleles in 76 Japanese patients. HLA-A, -B, and -C antigens were screened by the conventional typing method, and then B22-group alleles including HLA-B54 were genotyped by single-strand conformation polymorphism analysis. Alleles of HLA-DRB1 gene were fully determined by the microtiter plate hybridization method. Thirty-seven percent of the patients possessed HLA-B5401 allele conserved predominantly in East Asians, as compared with 15% of 110 healthy volunteers (chi2 = 12.4, p = 0.0004). In addition, 4% of the patients possessed B5504 also unique to Asians but a rare allele which was not found in normal control subjects in this study. Typing of HLA-DRB1 class II gene did not demonstrate strong positive association with the disease. A33, B44, and DRB1*1302 showed negative association with the disease. We conclude that distinctive molecular structure of HLA-B alleles or a closely linked gene in the HLA region contributes to genetic predisposition in diffuse panbronchiolitis. This may partly explain why this disorder is found primarily in Asians.

摘要

东亚地区的弥漫性泛细支气管炎(DPB)是一种病因不明的独特慢性阻塞性肺疾病。我们推测该疾病易感性归因于亚洲人特有的遗传易感性。此前已有关于人类白细胞抗原(HLA)-Bw54与该疾病关联的报道。在本研究中,我们使用新开发的基于聚合酶链反应(PCR)的方法,直接分析了76例日本患者的HLAⅠ类和Ⅱ类等位基因。通过传统分型方法筛选HLA-A、-B和-C抗原,然后通过单链构象多态性分析对包括HLA-B54在内的B22组等位基因进行基因分型。通过微量滴定板杂交法完全确定HLA-DRB1基因的等位基因。37%的患者拥有主要在东亚人中保守的HLA-B5401等位基因,相比之下,110名健康志愿者中有15%拥有该等位基因(χ2 = 12.4,p = 0.0004)。此外,4%的患者拥有同样为亚洲人所特有的B5504,但该等位基因罕见,在本研究的正常对照受试者中未发现。HLA-DRB1Ⅱ类基因分型未显示与该疾病有强阳性关联。A33、B44和DRB1*1302与该疾病呈负相关。我们得出结论,HLA-B等位基因独特的分子结构或HLA区域中紧密连锁的基因导致了弥漫性泛细支气管炎的遗传易感性。这可能部分解释了为何这种疾病主要在亚洲人当中出现。

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