Capture-ELISA for serum IgM antibody to respiratory syncytial virus.

R Cevenini, M Donati, S Bertini, A Moroni, V Sambri
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引用次数: 3

Abstract

A four-component solid-phase capture enzyme immunoassay was set up to test for serum IgM antibody to respiratory syncytial (RS) virus and was compared with immunofluorescence assay (IFA). A total of 128 young children with acute respiratory infections were studied. Thirty-six were shown to be RS virus-positive by the detection of RS virus in nasopharyngeal secretions and 92 were RS virus-negative. A serum specimen was collected after admission to the hospital (days 0-4) and a further specimen was obtained during days 10-14. Out of 36 RS virus-positive patients, 28 (77.7%) were found to be positive for IgM by both capture-ELISA and IFA. Out of 92 RS virus-negative patients 5 (5.4%) were IgM-positive. Four false-positive results were obtained by IFA due to the presence of rheumatoid factor. The capture-ELISA was shown to be a reliable technique in detecting specific IgM antibody to RS virus.

血清抗呼吸道合胞病毒IgM抗体的elisa测定。
建立四组分固相捕获酶免疫分析法检测血清呼吸道合胞病毒IgM抗体,并与免疫荧光法(IFA)进行比较。对128例急性呼吸道感染的幼儿进行了研究。鼻咽分泌物RS病毒检测呈阳性36例,RS病毒阴性92例。入院后(0-4天)采集血清标本,10-14天进一步采集标本。在36例RS病毒阳性患者中,28例(77.7%)经捕获- elisa和IFA检测均为IgM阳性。92例RS病毒阴性患者中5例(5.4%)为igm阳性。由于类风湿因子的存在,IFA有4个假阳性结果。捕获- elisa是一种检测RS病毒特异性IgM抗体的可靠方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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