Comparative evaluation of Abbott and Murex antibody assays and Roche Amplicor PCR for diagnosis of human hepatitis C

D. Liu, J. Steele, S. Lloyd Jones, D. Leslie, J. Pedersen, R. Baird
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Abstract

Of 135 serum samples from 135 patients suspected of hepatitis C virus (HCV) infection, 67 were detected by Abbott IMX antibody assay, 89 by Murex anti-HCV (version III), and 47 by Roche Amplicor polymerase chain reaction (PCR). Furthermore, 44 of the 62 positive serum samples by both Abbott and Murex antibody assays, 2 of the 27 positive samples by Murex antibody assay only, none of the 5 positive samples by Abbott antibody assay only, and one of the 43 negative samples by both Abbott and Murex antibody assays had measurable HCV RNA by Roche Amplicor PCR, suggesting active hepatitis C viremia. Whereas Abbott and Murex antibody assays were in agreement with each other in 103 of the 135 serum samples tested, they showed discrepancy with regard to the other 32. Despite generating a small percentage of false positives, Abbott and Murez antibody assays are useful in monitoring serum antibody levels of the past or continuing hepatitis C virus infection. Abbott IMX appears to be more specific than Murex anti-HCV (version III). The use of Roche Amplicor PCR provides a means of revealing active hepatitis C viremia, and helping clarify antibody indeterminate serum samples.

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雅培和Murex抗体检测与罗氏扩增PCR诊断丙型肝炎的比较评价
在135例疑似丙型肝炎病毒(HCV)感染患者的135份血清中,雅培(Abbott) IMX抗体检测67份,Murex抗HCV (III型)检测89份,罗氏(Roche)扩增聚合酶链反应(PCR)检测47份。此外,62份Abbott和Murex抗体检测均为阳性的血清样本中有44份,27份Murex抗体检测均为阳性的样本中有2份,5份Abbott抗体检测均为阳性的样本中没有一份,43份Abbott和Murex抗体检测均为阴性的样本中有1份通过Roche Amplicor PCR可检测到HCV RNA,提示活动性丙型肝炎病毒血症。虽然雅培和Murex抗体测定在135个血清样本中有103个相互一致,但在另外32个血清样本中却显示出差异。尽管产生小比例的假阳性,Abbott和Murez抗体测定法在监测过去或持续丙型肝炎病毒感染的血清抗体水平方面是有用的。雅培IMX似乎比Murex anti-HCV(版本III)更具特异性。使用罗氏扩增酶链反应提供了一种揭示活动性丙型肝炎病毒血症的方法,并有助于澄清抗体不确定的血清样本。
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Subject index Volume contents Author index The value of ELISA vs. negative Coombs findings in the serodiagnosis of human brucellosis Detection of toxoplasma-specific antibody in human saliva using conventional assays
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