Keicho N, Ohashi J, Tamiya G, Nakata K, Taguchi Y, Azuma A, Ohishi N, Emi M, Park M H, Inoko H, Tokunaga K, Kudoh S
Department of Respiratory Medicine, Graduate School of Medicine, University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Am J Hum Genet. 2000 Feb;66(2):501-7. doi: 10.1086/302786.
Diffuse panbronchiolitis affecting East Asians is strongly associated with the class I human leukocyte antigen (HLA) alleles. Recent observations suggest that a major disease-susceptibility gene may be located between the HLA-B and HLA-A loci in the class I region of the major histocompatibility complex on chromosome 6. To test this possibility, we analyzed 14 polymorphic markers in 92 Japanese patients and 93 healthy controls. Of these, seven marker alleles, including HLA-B54 and HLA-A11, were significantly associated with the disease. Maximum-likelihood haplotype analysis and subsequent direct determination of individual haplotypes identified a group of disease-associated haplotypes, one of which contained all seven disease-associated marker alleles. Another haplotype, containing HLA-B*5504, was also associated with the disease. All these haplotypes seem to have diverged from a common ancestral haplotype in East Asians and share a specific segment containing three consecutive markers between the S and TFIIH loci in the class I region. Furthermore, one of the markers within the candidate region showed the highest delta value, indicating the strongest association. Of 20 Korean patients with diffuse panbronchiolitis, 17 also shared the combination of the disease-associated marker alleles within the candidate region. These results indicate that an HLA-associated major susceptibility gene for diffuse panbronchiolitis is probably located within the 200 kb in the class I region 300 kb telomeric of the HLA-B locus on the chromosome 6p21.3.
影响东亚人的弥漫性泛细支气管炎与人类白细胞抗原(HLA)I类等位基因密切相关。最近的观察结果表明,主要的疾病易感基因可能位于6号染色体上主要组织相容性复合体I类区域的HLA - B和HLA - A基因座之间。为了验证这种可能性,我们分析了92例日本患者和93例健康对照中的14个多态性标记。其中,包括HLA - B54和HLA - A11在内的7个标记等位基因与该疾病显著相关。最大似然单倍型分析及随后对个体单倍型的直接测定确定了一组与疾病相关的单倍型,其中之一包含所有7个与疾病相关的标记等位基因。另一个包含HLA - B*5504的单倍型也与该疾病相关。所有这些单倍型似乎都源自东亚人的一个共同祖先单倍型,并在I类区域的S和TFIIH基因座之间共享一个包含三个连续标记的特定片段。此外,候选区域内的一个标记显示出最高的δ值,表明其关联性最强。在20例韩国弥漫性泛细支气管炎患者中,有17例在候选区域内也共享了与疾病相关的标记等位基因组合。这些结果表明,弥漫性泛细支气管炎的一个与HLA相关的主要易感基因可能位于6号染色体p21.3上HLA - B基因座端粒方向300 kb处I类区域的200 kb范围内。