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使用分子和血清学分型方法分析丙型肝炎病毒分离株。

Analysis of hepatitis C virus isolates using molecular and serological typing methods.

作者信息

Cretel E, Gallian P, Obadia Y, Rousseau S, de Micco P, de Lamballerie X

机构信息

Laboratoire de Virologie, Faculté de Médecine de Marseille, France.

出版信息

Acta Virol. 1997 Oct;41(5):269-75.

PMID:9607080
Abstract

This study comprised 100 persons with antibodies to hepatitis C virus (HCV), including 77 intravenous drug users (IVDUs). They were tested with serological HCV typing assays (Murex HCV serotyping 1-6 assay; Chiron RIBA HCV Serotyping SIA). Patients with a positive polymerase chain reaction (PCR) for HCV (n = 66) were tested with genotyping molecular assays (Inno-Lipa HCV II test; Sorin GEN-ETI-K HCV typing assay). Comparison of the results of these tests showed that (a) 92% of samples could be typed by one test at least; 44% could be typed by all four tests; 88% could be typed by one serological test at least and 66% by one molecular test at least; (b) 81% of the samples successfully tested with both serological tests gave comparable results; 95% of the samples successfully tested with both molecular tests gave comparable results; (c) when serological and molecular tests yielded different results, sequences in the 5'-non-coding (5' NC) or E1 regions always confirmed the results of the molecular tests; (d) in case of discrepancy between the results of the molecular tests the E1 region sequences confirmed the Sorin test results. It is concluded that the molecular tests compared gave similar results. The fact that the Murex serological test gave comparable results in more than 80% of cases indicates that it is an alternative to the molecular tests for routine diagnosis. However, comparison of the results of this test with those obtained in patients consulting a hepatology department showed that it gave the best results in a population of patients not exposed repeatedly to HCV.

摘要

本研究纳入了100名丙型肝炎病毒(HCV)抗体阳性者,其中包括77名静脉注射吸毒者(IVDU)。他们接受了血清学HCV分型检测(Murex HCV血清学分型1 - 6检测;Chiron RIBA HCV血清学分型SIA)。HCV聚合酶链反应(PCR)阳性的患者(n = 66)接受了基因分型分子检测(Inno - Lipa HCV II检测;Sorin GEN - ETI - K HCV分型检测)。这些检测结果的比较显示:(a)至少92%的样本可通过一项检测进行分型;44%的样本可通过全部四项检测进行分型;至少88%的样本可通过一项血清学检测进行分型,至少66%的样本可通过一项分子检测进行分型;(b)两项血清学检测均成功检测的样本中,81%得出了可比结果;两项分子检测均成功检测的样本中,95%得出了可比结果;(c)当血清学和分子检测结果不同时,5' - 非编码(5' NC)或E1区域的序列总是证实分子检测的结果;(d)在分子检测结果存在差异的情况下,E1区域序列证实了Sorin检测的结果。结论是所比较的分子检测得出了相似的结果。Murex血清学检测在超过80%的病例中得出了可比结果,这一事实表明它可作为常规诊断中分子检测的替代方法。然而,将该检测结果与肝病科就诊患者的检测结果进行比较显示,它在未反复接触HCV的患者群体中得出的结果最佳。

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