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一种独特的HLA - DRw8单倍型是青少年类风湿性关节炎患者的特征。

A distinct HLA-DRw8 haplotype characterizes patients with juvenile rheumatoid arthritis.

作者信息

Van Kerckhove C, Melin-Aldana H, Elma M S, Luyrink L, Donnelly P, Taylor J, Maksymowych W P, Lovell D J, Choi E, Glass D N

机构信息

Children's Hospital Medical Center, Cincinnati, OH.

出版信息

Immunogenetics. 1990;32(5):304-8. doi: 10.1007/BF00211643.

Abstract

We studied the first domain of the HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci of 67 HLA-DRw8-positive Caucasians including 43 with early-onset pauciarticular juvenile rheumatoid arthritis (EOPA-JRA, alternatively known as early-onset pauciarticular juvenile chronic arthritis). Serology, restriction fragment length polymorphism (RFLP), and polymerase chain reaction (PCR) oligotyping revealed that 62, including all the EOPA-JRA patients, carried the HLA-DRB10801, DQA10401, DQB10402 genotype. Approximately one-fifth of the controls carried atypical HLA-DRB1, HLA-DQA1, and/or HLA-DQB1 loci on their HLA-DRw8 haplotype confirmed by family studies. DNA sequences of HLA-DRB1, DQA1, and DQB1 alleles in patients and controls were identical to those previously reported. Disease association studies in 113 EOPA-JRA patients and 207 controls unselected for HLA-DRw8 revealed that the HLA-DRB10801, DQA10401, DQB10402 genotype was associated with a higher relative risk (RR) for disease (RR = 12.8, chi 2 = 48.8, P less than 10(-4)) than was the serologically defined presence of HLA-DRw8 (RR = 8, chi 2 = 39, P less than 10(-4)). Further analysis suggested that the DQ genes on HLA-DRw8 haplotypes are as likely as the DR genes to contribute to the pathogenesis of EOPA-JRA. This study increases to five the number of HLA-DR/DQ haplotypes identified in HLA-DRw8 Caucasians.

摘要

我们研究了67名HLA - DRw8阳性高加索人的HLA - DRB1、HLA - DQA1和HLA - DQB1基因座的第一个结构域,其中包括43名早发性少关节型幼年类风湿性关节炎(EOPA - JRA,也称为早发性少关节型幼年慢性关节炎)患者。血清学、限制性片段长度多态性(RFLP)和聚合酶链反应(PCR)寡核苷酸分型显示,62人(包括所有EOPA - JRA患者)携带HLA - DRB10801、DQA10401、DQB10402基因型。通过家系研究证实,约五分之一的对照在其HLA - DRw8单倍型上携带非典型的HLA - DRB1、HLA - DQA1和/或HLA - DQB1基因座。患者和对照中HLA - DRB1、DQA1和DQB1等位基因的DNA序列与先前报道的相同。在113名EOPA - JRA患者和207名未按HLA - DRw8选择的对照中进行的疾病关联研究表明,与血清学定义的HLA - DRw8存在相比,HLA - DRB10801、DQA10401、DQB10402基因型与疾病的相对风险(RR)更高(RR = 12.8,卡方 = 48.8,P小于10^(-4))(RR = 8,卡方 = 39,P小于10^(-4))。进一步分析表明,HLA - DRw8单倍型上的DQ基因与DR基因一样,可能参与EOPA - JRA的发病机制。这项研究将在HLA - DRw8高加索人中鉴定出的HLA - DR/DQ单倍型数量增加到了5种。

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