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Establishment and Evaluation of a One-Step Microplate Chemiluminescence Immunoassay to Detect IgG Antibody Against Treponema Pallidum

机译:一步法微孔板化学发光免疫分析法检测和鉴定梅毒螺旋体IgG抗体的建立与评价

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Background: The serological detection of specific antibodies against Treponema pallidum is of particular importance in the diagnosis of syphilis. The chemiluminescence immunoassay (CLIA) has been widely used for clinical diagnosis because they remit no radical waste products, cause no enzyme precipitation, and exhibit an excellent sensitivity. Methods: A one-step CLIA was established to detect T. pallidum IgG antibody based on microplate coated with a mixture of recombinant T. pallidum antigens TpN15, TpN17, and TpN47. The Chinese national reference substances standard panel for T. pallidum diagnosis was applied to test the accuracy, stability, interference, and cross-reactivity of the established CLIA. The validation of efficacy for clinical application was performed by comparing the established method with the marketed T. pallidum particle agglutination (TPPA) kit and the Abbott ARCHITEC Auto System. Results: The established method met the requirement of the Chinese national reference substances standard for T. pallidum diagnosis. When compared with TPPA (n = 1,052), the specificity, sensitivity, and overall concordance were 99.7%, 99.0%, and 98.8% respectively, showing a great agreement with a kappa value of 0.81. When compared with the Abbott ARCHITEC Auto System (n = 352), the results showed that the specificity, sensitivity, and overall concordance were 98.6.0%, 96.6% and 98.6% respectively, and a high-degree agreement was observed (kappa value = 0.95). Conclusion: The established rapid, specific, sensitive, and stable microplate CLIA method to detect IgG antibody against T pallidum will provide an efficient alternative to the treponemal tests and wide application in clinical laboratory. (C) 2014 Wiley Periodicals, Inc.
机译:背景:针对梅毒螺旋体的特异性抗体的血清学检测在梅毒的诊断中特别重要。化学发光免疫分析法(CLIA)已被广泛用于临床诊断,因为它们不释放自由基废物,不引起酶沉淀,并且显示出极好的敏感性。方法:建立基于一步法CLIA的检测方法,该方法基于涂有重组苍白螺旋体抗原TpN15,TpN17和TpN47混合物的微孔板,检测苍白螺旋体IgG抗体。应用中国国家标准物质梅毒螺旋体诊断标准小组来测试已建立的CLIA的准确性,稳定性,干扰性和交叉反应性。通过将建立的方法与市售的苍白锥颗粒凝集(TPPA)试剂盒和Abbott ARCHITEC Auto System进行比较,对临床应用的功效进行了验证。结果:所建立的方法符合中国国家参考物质标准对梅毒螺旋体的诊断要求。与TPPA(n = 1,052)相比,特异性,敏感性和总体一致性分别为99.7%,99.0%和98.8%,kappa值为0.81,显示出很好的一致性。与Abbott ARCHITEC Auto System(n = 352)进行比较时,结果显示特异性,敏感性和总体一致性分别为98.6.0%,96.6%和98.6%,并且观察到高度一致性(kappa值) = 0.95)。结论:已建立的快速,特异性,灵敏和稳定的微孔板CLIA方法可检测抗梅毒的IgG抗体,这将是对梅毒螺旋体检测的有效替代方法,并在临床实验室中得到广泛应用。 (C)2014威利期刊公司

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