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在重组免疫印迹法(RIBA)停用后,对实时定量聚合酶链反应作为丙型肝炎病毒补充检测方法的评估。

Evaluation of Quantitative Real-Time PCR as a Hepatitis C Virus Supplementary Test After RIBA Discontinuation.

作者信息

Gong Shunyou, Schmotzer Christine L, Zhou Lan

机构信息

Department of Pathology, University Hospitals Case Medical Center and Case Western Reserve University School of Medicine, Cleveland, Ohio.

出版信息

J Clin Lab Anal. 2016 Sep;30(5):418-23. doi: 10.1002/jcla.21873. Epub 2015 Oct 26.

Abstract

Laboratory testing plays a major role in hepatitis C virus (HCV) diagnosis and patient follow-up. The high false positive rates of HCV screening tests require confirmation through a supplementary test. According to the 2003 CDC guidelines, recombinant immunoblot assay (RIBA) is indispensible to confirm positive screening results and differentiate biologic false positivity from true HCV exposure. However, RIBA has been permanently discontinued since 2011. In the 2013 update of its guidelines, CDC called for further studies on HCV laboratory testing without RIBA. In this study, we analyzed the applicability of quantitative real-time PCR (qPCR) as a supplementary HCV diagnostic test. By comparing our HCV testing performances before and after RIBA discontinuation, we found that omitting RIBA has no significant effect on the accurate and efficient identification of HCV infection, provided that HCV antibody signal-to-cutoff ratio is considered. Furthermore, we proposed a new HCV testing algorithm that incorporates semiquantitative assessment of HCV antibody positivity and HCV viral load measurement by qPCR. By following the algorithm, we were able to address confirmation of positive HCV screening results and to provide useful information generally required by clinicians, including the needs of further laboratory testing or clinical follow-up, as well as HCV viral titers.

摘要

实验室检测在丙型肝炎病毒(HCV)诊断及患者随访中发挥着重要作用。HCV筛查试验的高假阳性率需要通过补充试验进行确认。根据2003年美国疾病控制与预防中心(CDC)的指南,重组免疫印迹试验(RIBA)对于确认筛查阳性结果以及区分生物学假阳性与真正的HCV暴露不可或缺。然而,RIBA自2011年起已永久停产。在其2013年更新的指南中,CDC呼吁对不使用RIBA的HCV实验室检测进行进一步研究。在本研究中,我们分析了定量实时聚合酶链反应(qPCR)作为补充性HCV诊断试验的适用性。通过比较RIBA停产前后我们的HCV检测性能,我们发现,若考虑HCV抗体信号与临界值之比,省略RIBA对准确、高效识别HCV感染并无显著影响。此外,我们提出了一种新的HCV检测算法,该算法纳入了HCV抗体阳性的半定量评估以及通过qPCR进行的HCV病毒载量测定。遵循该算法,我们能够解决HCV筛查阳性结果的确认问题,并提供临床医生通常所需的有用信息,包括进一步实验室检测或临床随访的需求以及HCV病毒滴度。

相似文献

本文引用的文献

10
Diagnosis of hepatitis C.丙型肝炎的诊断。
Hepatology. 1997 Sep;26(3 Suppl 1):48S-56S. doi: 10.1002/hep.510260709.

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