Singal D P, Li J, Zhu Y
Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Clin Exp Rheumatol. 2000 Jul-Aug;18(4):485-91.
We examined the contribution of the HLA class III region in susceptibility to rheumatoid arthritis (RA).
Patients with RA, healthy subjects and homozygous typing cell (HTC) lines were typed for HLA class I (A, B, C), class II (DR, DQ) and class III (D6S273, Bat 2, and TNFa microsatellites, and HSP70 promoter region) alleles by molecular techniques.
Based on the distribution of microsatellites D6S273, Bat2 and TNFa, and HSP70 promoter region alleles in HTCs and homozygous unrelated individuals, a class III region haplotype, D6S273 138-HSP70c-Bat2 138-TNFa2 was identified. This haplotype showed a significant primary association with susceptibility to RA in DRB 1 QKRAA/QRRAA epitope-negative patients.
Since the QKRAA/QRRAA epitope does not provide any risk for disease susceptibility in RA-susceptibility DRB1 epitope-negative patients, the present data suggest that the class III region haplotype D6S273 138-HSP70c-Bat2 138-TNFa2 provides an additional risk for the development of RA. These results show that two regions in MHC, class II (DRB1) and class III (D6S273 138-HSP70c-Bat 2 138-TNFa2), contribute to susceptibility to RA and more completely define the risk for development of the disease.
我们研究了人类白细胞抗原(HLA)Ⅲ类区域在类风湿关节炎(RA)易感性中的作用。
采用分子技术对RA患者、健康受试者和纯合分型细胞(HTC)系进行HLAⅠ类(A、B、C)、Ⅱ类(DR、DQ)和Ⅲ类(D6S273、Bat2、肿瘤坏死因子α微卫星以及热休克蛋白70启动子区域)等位基因分型。
根据HTC系和纯合无关个体中微卫星D6S273、Bat2、肿瘤坏死因子α以及热休克蛋白70启动子区域等位基因的分布,确定了一种Ⅲ类区域单倍型,即D6S273 138 - HSP70c - Bat2 138 - TNFa2。在DRB1 QKRAA/QRRAA表位阴性的患者中,该单倍型与RA易感性存在显著的原发性关联。
由于在RA易感性DRB1表位阴性的患者中,QKRAA/QRRAA表位并未提供任何疾病易感性风险,目前的数据表明Ⅲ类区域单倍型D6S273 138 - HSP70c - Bat2 138 - TNFa2为RA的发生提供了额外风险。这些结果表明,主要组织相容性复合体(MHC)中的两个区域,即Ⅱ类(DRB1)和Ⅲ类(D6S273 138 - HSP70c - Bat2 138 - TNFa2),与RA易感性相关,并更全面地确定了该疾病发生的风险。