Yoshida M, Kimura A, Katsuragi K, Numano F, Sasazuki T
Department of Genetics, Kyushu University, Fukuoka, Japan.
Tissue Antigens. 1993 Aug;42(2):87-90. doi: 10.1111/j.1399-0039.1993.tb02242.x.
Sixty-four patients with Takayasu's arteritis and 156 healthy individuals in the Japanese population were examined for HLA-B specificity at the DNA level by DNA typing using polymerase chain reaction (PCR)/sequence-specific oligonucleotide probe (SSOP) analysis and by subsequent sequencing analysis. The frequency of epitope combination group-B52 (EC-B52) corresponding precisely to HLA-B52 specificity and that of EC-B39.2 which is a newly-identified subtype of HLA-B39 specificity were increased in the patient group. These two disease-associated HLA-B alleles share an epitope composed of 63Glu and 67Ser. Because two HLA-B alleles, HLA-B51 and B39.1, which are similar but different at the epitope from HLA-B52 and B39.2, respectively, are not associated with Takayasu arteritis, 63Glu and 67Ser are supposed to be involved in the pathogenesis.
对64例大动脉炎患者和156名日本健康人群,采用聚合酶链反应(PCR)/序列特异性寡核苷酸探针(SSOP)分析进行DNA分型,并通过后续测序分析在DNA水平检测HLA - B特异性。在患者组中,与HLA - B52特异性精确对应的表位组合组 - B52(EC - B52)以及作为HLA - B39特异性新鉴定亚型的EC - B39.2的频率增加。这两个与疾病相关的HLA - B等位基因共享一个由63Glu和67Ser组成的表位。由于两个HLA - B等位基因HLA - B51和B39.1,分别在表位上与HLA - B52和B39.2相似但不同,且与大动脉炎无关,因此推测63Glu和67Ser参与了发病机制。