Kimura A, Kobayashi Y, Takahashi M, Ohbuchi N, Kitamura H, Nakamura T, Satoh M, Sasaoka T, Hiroi S, Arimura T, Akai J, Aerbajinai W, Yasukochi Y, Numano F
Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University, Japan.
Int J Cardiol. 1998 Oct 1;66 Suppl 1:S107-13; discussion S115. doi: 10.1016/s0167-5273(98)00157-0.
To further clarify the HLA-linked genes susceptible to arterio-vasculitis of unknown etiology, Takayasu's arteritis and Buerger's disease, polymorphism in the MICA gene, a newly identified gene near the HLA-B gene and expressed in epithelial cell lineage, was investigated. Polymerase chain reaction (PCR)-DNA conformation polymorphism (DCP) analysis and subsequent sequencing of the MICA gene have revealed that there are 5 MICA alleles which are different in the number of a GCT repeat in exon 5: MICA alleles MICA-1.1, -1.2, -1.3 and -1.4 have 9, 6, 5 and 4 GCT repeats, respectively, and MICA-1.5 has 5 GCT repeats with a 1 bp frameshift insertion in the repeat. MICA genotyping data in 81 Japanese patients with Takayasu's arteritis, 38 Japanese patients with Buerger's disease, and 160 healthy Japanese controls showed that MICA-1.2 and -1.4 were significantly associated with Takayasu's arteritis and Buerger's disease, respectively. Because MICA-1.2 and -1.4 were in strong linkage disequilibria with HLA-B52 and -B54 in the Japanese populations, respectively, we have compared the odds ratio (OR) of the risk to the diseases for individuals having both or each of the disease-associated MICA and HLA-B alleles. It was found that MICA-1.2 gave a significantly high OR of risk to Takayasu's arteritis in the absence of HLA-B52, suggesting that the HLA-linked gene susceptible to Takayasu's arteritis is mapped near the MICA gene. In contrast, MICA-1.4 gave a significantly high OR of risk to Buerger's disease only in the presence of HLA-B54, suggesting that the HLA-linked gene susceptible to Buerger's disease is linked to the HLA-B54-MICA-1.4 haplotype, and may be differently mapped from that to Takayasu's arteritis.
为了进一步阐明与病因不明的动血管炎、高安动脉炎和血栓闭塞性脉管炎相关的HLA连锁基因,我们研究了MICA基因的多态性,该基因是在HLA - B基因附近新发现的基因,在上皮细胞谱系中表达。聚合酶链反应(PCR)-DNA构象多态性(DCP)分析以及随后对MICA基因的测序表明,有5个MICA等位基因,其外显子5中GCT重复序列的数量不同:MICA等位基因MICA - 1.1、-1.2、-1.3和-1.4分别有9、6、5和4个GCT重复序列,而MICA - 1.5有5个GCT重复序列,且在重复序列中有1个碱基对的移码插入。81例日本高安动脉炎患者、38例日本血栓闭塞性脉管炎患者和160例健康日本对照的MICA基因分型数据显示,MICA - 1.2和-1.4分别与高安动脉炎和血栓闭塞性脉管炎显著相关。由于在日本人群中,MICA - 1.2和-1.4分别与HLA - B52和- B54处于强连锁不平衡状态,我们比较了同时具有或分别具有疾病相关MICA和HLA - B等位基因的个体患疾病风险的比值比(OR)。结果发现,在没有HLA - B52的情况下,MICA - 1.2使高安动脉炎的患病风险OR显著升高,这表明与高安动脉炎相关的HLA连锁基因定位于MICA基因附近。相反,MICA - 1.4仅在存在HLA - B54的情况下使血栓闭塞性脉管炎的患病风险OR显著升高,这表明与血栓闭塞性脉管炎相关的HLA连锁基因与HLA - B54 - MICA - 1.4单倍型连锁,并且其定位可能与高安动脉炎不同。