Kimura A, Kitamura H, Date Y, Numano F
Department of Tissue Physiology, Tokyo Medical and Dental University, Japan.
Int J Cardiol. 1996 Aug;54 Suppl:S61-9. doi: 10.1016/s0167-5273(96)88774-2.
To identify an HLA-linked susceptibility gene to Takayasu's arteritis, comprehensive analysis of HLA genes was performed. By serologic HLA typing, positive associations of Takayasu's arteritis with HLA-B52 and B39 were observed. The DNA typing of HLA-B gene and class II genes (DRB1, DQA1, DPB1) showed positive associations of the disease with HLA-B52, B39.2, DRB1 * 1502 and DPB1 * 0901, confirming in part the serologic observations. Comparison of odds ratio for the risk of disease revealed that HLA-B52 and B39.2 were primarily involved in the susceptibility, while the associations with DRB1 * 1502 and DPB1 * 0901 were suggested to reflect a strong linkage disequilibrium of these class II alleles with HLA-B52 in the Japanese population. Sequencing analyses of HLA-B52 and B39.2 from patients confirmed that they were B 5201 and B 3902, respectively. Comparison of amino acid sequences of these disease-associated HLA-B alleles identified critical amino acid residues of the HLA-B molecule, Glu and Ser at 63rd and 67th positions, respectively, which may determine the susceptibility to Takayasu's arteritis via binding and presenting a yet unknown disease-related antigen.
为了鉴定与大动脉炎相关的HLA连锁易感基因,我们对HLA基因进行了全面分析。通过血清学HLA分型,观察到大动脉炎与HLA - B52和B39呈正相关。HLA - B基因和II类基因(DRB1、DQA1、DPB1)的DNA分型显示,该疾病与HLA - B52、B39.2、DRB1 * 1502和DPB1 * 0901呈正相关,部分证实了血清学观察结果。疾病风险比值比的比较显示,HLA - B52和B39.2主要参与易感性,而与DRB1 * 1502和DPB1 * 0901的关联表明,在日本人群中,这些II类等位基因与HLA - B52存在强烈的连锁不平衡。对患者的HLA - B52和B39.2进行测序分析证实,它们分别为B5201和B3902。对这些与疾病相关的HLA - B等位基因的氨基酸序列进行比较,确定了HLA - B分子的关键氨基酸残基,分别为第63位的Glu和第67位的Ser,它们可能通过结合并呈递一种未知的疾病相关抗原来决定对大动脉炎的易感性。