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Reliability of four methods for the diagnosis of acute infection by Epstein‐Barr virus

机译:四种诊断爱泼斯坦-巴尔病毒急性感染方法的可靠性

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We studied the reliability of new indirect tests in the diagnosis of acute infection by Epstein‐Barr virus (EBV). Studied for all samples were: method 1, the heterophil antibodies (Abs) (Monolatex, Biokit, Germany); method 2, the IgM Abs to EBV with ELISA tests (antigen pools, Enzygnost, Behringwerke, Germany); method 3, EA (Biotest Diagnostics, Germany); and method 4, the IgG avidity test. The reliability of the four tests for the detection of primary infection by EBV was: sensitivity (method 1:89.1%; method 2: 100%; method 3: 79.7%; method 4: 99%); specificity (method 1: 98%; method 2: 100%; method 3:84%; method 4: 100%); positive predictive value (method 1: 97.6%; method 2: 100%; method 3: 73.6%; method 4: 100% method 4: 100%), and negative predictive value (method 1: 90.7%; method 2: 100%; method 3:84%; method 4: 99%). The IgG avidity test (method 4) is simple and automated in the laboratory and is very useful for ascertaining, from a single sample, the time since infection. It is criteria of recent primoinfection higher levels than 55% of IgG with low avidity for the antigen. The investigation of the Abs to antigen pools (method 2) by ELISA of virus had a high reliability, but the investigation of heterophil Abs by latex (method 1) and the Abs IgM to EA (method 2) were lacking in sensibility regarding their use in the diagnosis of the primoinfection. J. Clin. Lab. Anal. 11:78–81. © 1997 Wiley‐Liss, Inc.
机译:我们研究了新的间接测试在诊断爱泼斯坦-巴尔病毒(EBV)急性感染中的可靠性。研究的所有样品为:方法1,异源抗体(Abs)(Monolatex,Biokit,德国);方法2,采用ELISA试验(免疫原,Enzygnost,德国贝林沃克,德国)对EBV的IgM抗体进行检测;方法3,EA(德国Biotest Diagnostics);和方法4,IgG亲和力测试。四种检测EBV原发感染的方法的可靠性是:敏感性(方法1:89.1%;方法2:100%;方法3:79.7%;方法4:99%);灵敏度(方法1)。特异性(方法1:98%;方法2:100%;方法3:84%;方法4:100%);阳性预测值(方法1:97.6%;方法2:100%;方法3:73.6%;方法4:100%方法4:100%)和阴性预测值(方法1:1:90.7%;方法2:100% ;方法3:84%;方法4:99%)。 IgG亲和力测试(方法4)在实验室中简单且自动化,对于从单个样本确定感染后的时间非常有用。最近的一次原发感染的标准是高于55%的IgG,且抗原亲和力低。通过病毒ELISA对Abs至抗原库的研究(方法2)具有很高的可靠性,但是对乳胶(方法1)和Abs IgM对EA的异源Abs研究(方法2)缺乏使用敏感性。在原发感染的诊断中。 J.临床实验室肛门11:78–81。 ©1997 Wiley‐Liss,Inc.

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