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抗 Ro52 抗体与混合性结缔组织病肺纤维化的相关性。

Associations between anti-Ro52 antibodies and lung fibrosis in mixed connective tissue disease.

机构信息

Rheumatology Unit, Oslo University Hospital Rikshospitalet,

Department of Immunology and Transfusion Medicine, Oslo University Hospital.

出版信息

Rheumatology (Oxford). 2016 Jan;55(1):103-8. doi: 10.1093/rheumatology/kev300. Epub 2015 Aug 28.

DOI:10.1093/rheumatology/kev300
PMID:26320136
Abstract

OBJECTIVE

MCTD is a chronic, immune-mediated disorder defined by the combined presence of serum anti-RNP antibodies and distinct clinical features, including progressive lung fibrosis. The aim of the study was to evaluate the potential impact of anti-SSA (i.e. Ro52 and Ro60) and anti-SSB autoantibodies as markers for disease outcomes in MCTD.

METHODS

Stored serum samples from 113 patients included in the cross-sectional, nationwide Norwegian MCTD cohort were screened for the presence of anti-Ro52, anti-Ro60 and anti-SSB by a commercial line immunoassay. Correlation analyses were carried out with clinical parameters, including quantitative lung fibrosis scores by high-resolution CT. Lung fibrosis was defined by reticular pattern changes according to the Fleischner Society CT criteria for interstitial lung disease.

RESULTS

Anti-Ro52 antibodies were present in 29%, anti-Ro60 in 19% and anti-SSB in 6% of the MCTD sera. High-resolution CT scoring identified lung fibrosis in 38 of 113 (34%) MCTD patients. Anti-Ro52 antibodies were detected in 50% (19 of 38) of the MCTD patients with lung fibrosis and in 19% (14 of 75) without lung fibrosis (P < 0.001). The odds ratio for the presence of anti-Ro52 antibodies in lung fibrosis was 4.4 (95% CI 1.8, 10.3). Anti-Ro52 antibodies were equally frequent in patients with mild to moderate (eight of 17; 44%) and severe fibrosis (11 of 21; 52%). Anti-Ro52 was not associated with any of the other clinical parameters assessed, nor was anti-Ro60 or anti-SSB.

CONCLUSION

Our cross-sectional data suggest that anti-Ro52 antibodies may serve as a potential marker for lung fibrosis in MCTD.

摘要

目的

MCTD 是一种慢性、免疫介导的疾病,其特征是血清中存在抗 RNP 抗体和独特的临床特征,包括进行性肺纤维化。本研究旨在评估抗 SSA(即 Ro52 和 Ro60)和抗 SSB 自身抗体作为 MCTD 疾病结局的潜在标志物。

方法

通过商业线免疫分析法检测 113 例纳入横断面全国挪威 MCTD 队列的患者血清中抗 Ro52、抗 Ro60 和抗 SSB 的存在情况。对临床参数(包括高分辨率 CT 定量肺纤维化评分)进行相关性分析。肺纤维化根据 Fleischner 协会 CT 标准定义为间质性肺疾病的网状模式改变。

结果

在 113 例 MCTD 血清中,抗 Ro52 抗体的存在率为 29%,抗 Ro60 为 19%,抗 SSB 为 6%。高分辨率 CT 评分显示,113 例 MCTD 患者中有 38 例(34%)存在肺纤维化。肺纤维化患者中检测到抗 Ro52 抗体的有 50%(19/38),无肺纤维化患者中检测到抗 Ro52 抗体的有 19%(14/75)(P<0.001)。抗 Ro52 抗体在肺纤维化患者中的存在的比值比为 4.4(95%CI 1.8, 10.3)。在轻度至中度纤维化患者中(17 例中有 8 例,44%)和严重纤维化患者中(21 例中有 11 例,52%),抗 Ro52 抗体的频率相等。抗 Ro52 抗体与评估的任何其他临床参数均无相关性,抗 Ro60 抗体或抗 SSB 抗体也无相关性。

结论

我们的横断面数据表明,抗 Ro52 抗体可能是 MCTD 肺纤维化的潜在标志物。

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