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

机译:ELISA方法的诊断准确性,可以作为间接免疫荧光检测抗核抗体的替代筛选测试。评估五个商业套件。

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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.
机译:抗核抗体(ANA)的检测是诊断系统性自身免疫疾病的基本实验室测试。目前,选择的方法是在HEp-2细胞基质上进行间接免疫荧光(IIF)。这项研究的目的是评估用于ANA检测的五种市售酶免疫测定(EIA)试剂盒的诊断准确性,并验证将其用作IIF方法的替代方法的可能性。这项研究涉及1513例患者,其中315例被诊断为系统性自身免疫性疾病,另外1198例患者排除了自身免疫性疾病。对于所有血清,通过IIF和五种不同的EIA试剂盒进行ANA检测。评估结果与临床诊断以及可能存在的特异性自身抗体(抗-ENA或抗-dsDNA)有关;最后,将它们与使用ANA-IIF作为参考方法获得的结果进行比较。全身性自身免疫性疾病受试者的ANA-IIF测试阳性率为92%,而在五种ANA-EIA试剂盒中,应答方面的差异很大,阳性率为74%至94%。所有EIA试剂盒都能正确检测出导致均质和斑点荧光模式的抗体(抗dsDNA,抗RNP,抗Ro / SSA)的存在,但同时它们显示出核仁模式的实质性错误,其平均值为在这种情况下,灵敏度约为50%。取而代之的是,在鉴定抗Scl70和着丝粒模式方面,试剂盒之间存在很大差异,其敏感性分别为45%至91%和49%至100%。研究结果表明,市售的ANA-EIA试剂盒显示出不同水平的敏感性和特异性。它们中的一些具有与IIF方法相当的诊断准确性,在某些情况下甚至更高。因此,这些可用作IIE的替代筛选测试。但是,其他人不能确保可接受的结果。因此,在将这些方法中的任何一种纳入临床和诊断测试之前,建议对市场上的各种试剂盒进行仔细评估。

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