首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Association between radiographic severity of rheumatoid arthritis and shared epitope alleles: differing mechanisms of susceptibility and protection.
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Association between radiographic severity of rheumatoid arthritis and shared epitope alleles: differing mechanisms of susceptibility and protection.

机译:类风湿关节炎的影像学严重程度与共有的表位等位基因之间的关联:敏感性和保护作用的不同机制。

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OBJECTIVE: To investigate the association of a recently described classification of Human leukocyte antigen (HLA)-DRB1 shared epitope alleles with rheumatoid factors (RF) and anti-cyclic citrullinated peptide (CCP) production and radiological severity in rheumatoid arthritis (RA). METHODS: Patients with RA (n = 962) were studied. Genotyping of DRB1 alleles and assays for RF and anti-CCP were performed. Radiological severity was measured using the modified Larsen score. RESULTS: In accordance with previous reports, we found carriage of S2 alleles (K-R-A-A at positions 71-74) to be associated with more severe disease with a gene-dose effect (p = 0.0059), and also associated with the presence of anti-CCP and RF (p<0.001). Carriage of S1 alleles (D-E-R-A-A at positions 70-74) was associated with less severe disease (p = 0.01), however there was no association between S1 and either anti-CCP or RF, suggesting that the basis for this possible protective effect was not related to autoantibody-producing B cells. CONCLUSIONS: These data suggest that multiple biological mechanisms underlie the DRB1 association with rheumatoid arthritis severity.
机译:目的:研究最近描述的人类白细胞抗原(HLA)-DRB1共有表位等位基因分类与类风湿因子(RF)和抗环瓜氨酸肽(CCP)的产生以及类风湿关节炎(RA)的放射学严重性的关系。方法:研究了RA(962例)患者。进行了DRB1等位基因的基因分型以及RF和抗CCP的检测。使用改良的Larsen评分测量放射线严重程度。结果:根据先前的报告,我们发现S2等位基因(71-74位的KRAA)携带与更严重的疾病有关,具有基因剂量效应(p = 0.0059),还与抗CCP和RF(p <0.001)。 S1等位基因(DERAA在70-74位)的携带与病情较轻相关(p = 0.01),但是S1与抗CCP或RF之间没有关联,表明这种可能的保护作用的基础不是与产生自身抗体的B细胞有关。结论:这些数据表明DRB1与类风湿关节炎严重程度相关的多种生物学机制。

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