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生物治疗对抗双链DNA和抗核小体检测的影响。

The impact of biological treatments on the anti-dsDNA and anti-nucleosome tests.

作者信息

Infantino M, Grossi V, Benucci M, Li Gobbi F, Damiani A, Manfredi M

机构信息

1 Immunology and Allergology Laboratory Unit, S. Giovanni di Dio Hospital, Florence, Italy.

2 Rheumatology Unit, S. Giovanni di Dio Hospital, Florence, Italy.

出版信息

Lupus. 2018 Jan;27(1):40-48. doi: 10.1177/0961203317709344. Epub 2017 Jun 6.

Abstract

Background Anti-double stranded DNA antibodies are a very heterogeneous group of antibodies, quite specific for systemic lupus erythematosus. Newer technologies, such as addressable laser bead immunoassays (ALBIA), show great potential as a diagnostic application. The production of anti-double stranded DNA antibodies is often encountered in inflammatory arthritis; however, literature reports that the actual onset of drug induced lupus in patients treated with biological drugs is a rare event. False positive results for anti-double stranded DNA and anti-nucleosome antibodies detected in patients with inflammatory arthritis treated with different biologics prompted the investigation of full autoantibody profiles to evaluate each biomarker's diagnostic performance in systemic lupus erythematosus. The aim of the study was to compare the diagnostic performance of anti-double stranded DNA antibody and anti-nucleosome antibody methods and to evaluate the value of simultaneously measuring anti-double stranded DNA and anti-nucleosome antibodies, along with other anti-nuclear antibody analytes, as biomarkers for systemic lupus erythematosus, using a more appropriate control cohort including inflammatory arthritis patients with a non-clinical drug induced lupus. Methods Anti-double stranded DNA and anti-nucleosome antibody levels were evaluated in 247 patient samples: 70 systemic lupus erythematosus, 177 disease controls (including 97 inflammatory arthritis during treatment with different biologics) using the Bio-Rad BioPlex® 2200. Results Anti-nucleosome antibodies demonstrated greater clinical sensitivity and specificity than anti-double stranded DNA antibodies. At the manufacturers' cut-off range, considering the two markers as a single or combined test, the "anti-double stranded DNA test or anti-nucleosome antibodies" was the most sensitive combination (0.400) with the best negative likelihood ratio (0.62) and negative predictive value (0.803). Conclusion Anti-nucleosome antibodies are a more sensitive and specific biomarker of systemic lupus erythematosus than anti-double stranded DNA antibodies. Anti-nucleosome antibodies and anti-double stranded DNA antibodies are independent and complementary markers of systemic lupus erythematosus diagnosis and, therefore, are strongly suggested as combined tests (positive predictive value = 0.938). Moreover, the combined use of the two tests may help to overcome the decreased specificity percentage of the anti-double stranded DNA test, when considering an inflammatory arthritis cohort under biological therapies. The ALBIA method for anti-nuclear specificity detection allows a full autoantibody assessment, resulting in a much higher clinical specificity for systemic lupus erythematosus in the presence of ≥3 positive markers and significantly more positive likelihood ratio when ≥2 positive markers are present.

摘要

背景 抗双链DNA抗体是一类非常异质性的抗体,对系统性红斑狼疮具有较高的特异性。诸如可寻址激光珠免疫分析(ALBIA)等新技术在诊断应用方面显示出巨大潜力。抗双链DNA抗体的产生在炎性关节炎中经常出现;然而,文献报道接受生物药物治疗的患者中药物性狼疮的实际发病是罕见事件。在接受不同生物制剂治疗的炎性关节炎患者中检测到抗双链DNA和抗核小体抗体的假阳性结果,促使对全自身抗体谱进行研究,以评估每种生物标志物在系统性红斑狼疮中的诊断性能。本研究的目的是比较抗双链DNA抗体和抗核小体抗体方法的诊断性能,并评估同时检测抗双链DNA和抗核小体抗体以及其他抗核抗体分析物作为系统性红斑狼疮生物标志物的价值,使用一个更合适的对照队列,包括患有非临床药物性狼疮的炎性关节炎患者。方法 使用Bio-Rad BioPlex® 2200对247份患者样本中的抗双链DNA和抗核小体抗体水平进行评估:70例系统性红斑狼疮患者,177例疾病对照(包括97例在接受不同生物制剂治疗期间的炎性关节炎患者)。结果 抗核小体抗体显示出比抗双链DNA抗体更高的临床敏感性和特异性。在制造商设定的临界值范围内,将这两种标志物视为单一或联合检测时,“抗双链DNA检测或抗核小体抗体”是最敏感的组合(0.400),具有最佳的阴性似然比(0.62)和阴性预测值(0.803)。结论 抗核小体抗体是系统性红斑狼疮比抗双链DNA抗体更敏感和特异的生物标志物。抗核小体抗体和抗双链DNA抗体是系统性红斑狼疮诊断的独立且互补的标志物,因此强烈建议作为联合检测(阳性预测值 = 0.938)。此外,在考虑生物治疗下的炎性关节炎队列时,两种检测方法的联合使用可能有助于克服抗双链DNA检测特异性百分比的降低。用于抗核特异性检测的ALBIA方法允许进行全自身抗体评估,在存在≥3个阳性标志物时,对系统性红斑狼疮具有更高的临床特异性,并且在存在≥2个阳性标志物时具有显著更高的阳性似然比。

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