Hua Li, Yonghe Hu, Tao Zhang, Yang Liu, Yantang Wang, Tai Yang, Minhui Li, Qiaoli Luo, Yu Cheng, Qiang Zou
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引用次数: 4
摘要
WTCCC之前的全基因组关联研究发现了英国常见自身免疫性疾病的许多易感位点,包括类风湿性关节炎(RA)。由于类风湿关节炎的遗传异质性,有必要在其他人群中复制这些易感位点。本研究分析了3个在英国人中具有强RA关联信号的snp,并在汉族人群中首次对2个snp (rs6457617和rs11761231)进行了基因分型。在测试队列中,rs6457617与RA显著相关。携带纯合子基因型CC的个体比携带野生型基因型TT的个体有0.39倍的风险(P = 0.004, OR 0.39, [95% CI 0.21-0.74])。在另一个1514份样本的验证队列中,证实了等位基因C的保护作用(P基因型CC/TT = 5.9 × 10(-10), OR 0.34, [95% CI 0.24-0.48])。rs6457617可作为编码MHC-II α链的HLA-DQA1 * 03的标记snp。由于MHC限制在阳性选择和阴性选择阶段对原代t细胞很重要,MHC蛋白多态性可能与t细胞库的形成有关,包括炎性关节炎中t细胞克隆的出现。
Replication of british rheumatoid arthritis susceptibility Loci in two unrelated chinese population groups.
Previous genome-wide association study by WTCCC identified many susceptibility loci of common autoimmune diseases in British, including rheumatoid arthritis (RA). Because of the genetic heterogeneity of RA, it is necessary to replicate these susceptibility loci in other populations. Here, three SNPs with strong RA association signal in the British were analyzed in Han Chinese, and two SNPs (rs6457617 and rs11761231) were genotyped in the test cohort firstly. The rs6457617 was significantly associated with RA in the test cohort. The individuals bearing the homozygous genotype CC had 0.39-fold risk than these bearing the wild-type genotype TT (P = 0.004, OR 0.39, [95% CI 0.21-0.74]). And the protective effect of allele C was confirmed in another validation cohort with 1514 samples (P genotye CC/TT = 5.9 × 10(-10), OR 0.34, [95% CI 0.24-0.48]). The rs6457617 can be used as a tagSNP of HLA-DQA1∗03 which encoded MHC-II α chain. Since MHC restriction is important for primary T-cells in positive selection and negative selection stages, MHC protein polymorphisms may be implicated in shaping the T-cell repertoire, including the emergence of a T-cell clone involved in the inflammatory arthritis.