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酶联免疫吸附测定(ELISA)方法作为间接免疫荧光法检测抗核抗体的替代筛查试验的诊断准确性。对五种商用试剂盒的评估。

Diagnostic accuracy of ELISA methods as an alternative screening test to indirect immunofluorescence for the detection of antinuclear antibodies. Evaluation of five commercial kits.

作者信息

Tonuttia Elio, Bassetti Danila, Piazza Anna, Visentini Daniela, Poletto Monica, Bassetto Franca, Caciagli Patrizio, Villalta Danilo, Tozzoli Renato, Bizzaro Nicola

机构信息

Laboratorio Analisi Cliniche, Ospedale S. Maria della Misericordia, Udine, Italy.

出版信息

Autoimmunity. 2004 Mar;37(2):171-6. doi: 10.1080/08916930310001657010.

Abstract

Detection of antinuclear antibodies (ANA) is a fundamental laboratory test for diagnosing systemic autoimmune diseases. Currently, the method of choice is indirect immunofluorescence (IIF) on a HEp-2 cell substrate. The goal of this study was to evaluate the diagnostic accuracy of five commercially available enzyme immunoassay (EIA) kits for ANA detection and to verify the possibility of using them as an alternative to the IIF method. The study involved 1513 patients, 315 of whom were diagnosed with a systemic autoimmune disease and 1198 in whom an autoimmune disorder was excluded. For all sera, ANA detection was performed via IIF and with five different EIA kits. The results were evaluated in relation to clinical diagnosis and the presence of possible specific autoantibodies (anti-ENA or anti-dsDNA); lastly, they were compared with the results obtained using ANA-IIF as the method of reference. The positive rate of the ANA-IIF test in subjects with systemic autoimmune diseases was 92%, whereas in the five ANA-EIA kits there was broad diversity in terms of response, with positive rates ranging from 74 to 94%. All the EIA kits correctly detected the presence of antibodies (anti-dsDNA, anti-RNP, anti-Ro/SSA) responsible for homogeneous and speckled fluorescence pattern, but at the same time they showed substantial inaccuracy with the nucleolar pattern, with a mean sensitivity of approximately 50% in this case. Instead, there was a large kit-to-kit difference in terms of identification of anti-Scl70 and centromere patterns, for which sensitivities ranged between 45 and 91%, and between 49 and 100%, respectively. The results of the study demonstrate that the commercially available ANA-EIA kits show different levels of sensitivity and specificity. Some of them have a diagnostic accuracy that is comparable and, in some cases, even higher than the IIF method. Consequently, these could be used as an alternative screening test to IIE. However, others do not ensure acceptable results. Therefore, careful evaluation of the various kits on the market is advisable before including any of these methods in the clinical and diagnostic testing.

摘要

抗核抗体(ANA)检测是诊断系统性自身免疫性疾病的一项基本实验室检查。目前,首选方法是在人喉表皮癌细胞(HEp-2)基质上进行间接免疫荧光法(IIF)检测。本研究的目的是评估五种市售酶免疫分析(EIA)试剂盒检测ANA的诊断准确性,并验证其作为IIF法替代方法的可能性。该研究纳入了1513例患者,其中315例被诊断为系统性自身免疫性疾病,1198例排除自身免疫性疾病。对所有血清样本均通过IIF法以及使用五种不同的EIA试剂盒进行ANA检测。根据临床诊断以及是否存在可能的特异性自身抗体(抗可提取性核抗原抗体或抗双链DNA抗体)对结果进行评估;最后,将结果与以ANA-IIF法作为参考方法所获得的结果进行比较。系统性自身免疫性疾病患者中ANA-IIF检测的阳性率为92%,而在五种ANA-EIA试剂盒中,反应情况存在很大差异,阳性率在74%至94%之间。所有EIA试剂盒均能正确检测出导致均质型和斑点型荧光模式的抗体(抗双链DNA抗体、抗核糖核蛋白抗体、抗Ro/SSA抗体),但同时它们在核仁型荧光模式检测方面存在显著误差,在这种情况下平均灵敏度约为50%。相反,在抗Scl70抗体和着丝粒型荧光模式的识别方面,不同试剂盒之间存在很大差异,其灵敏度分别在45%至91%以及49%至100%之间。研究结果表明,市售ANA-EIA试剂盒的灵敏度和特异性水平各不相同。其中一些试剂盒的诊断准确性相当,在某些情况下甚至高于IIF法。因此,这些试剂盒可作为IIF法的替代筛查试验。然而,其他试剂盒无法保证获得可接受的结果。所以,在将这些方法中的任何一种纳入临床诊断检测之前,建议仔细评估市场上的各种试剂盒。

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