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Improved version 2.0 qualitative and quantitative AMPLICOR reverse transcription-PCR tests for hepatitis C virus RNA: calibration to international units, enhanced genotype reactivity, and performance characteristics.丙型肝炎病毒RNA的改进版2.0定性和定量AMPLICOR逆转录-聚合酶链反应检测:国际单位校准、增强的基因型反应性及性能特征
J Clin Microbiol. 2000 Nov;38(11):4171-9. doi: 10.1128/JCM.38.11.4171-4179.2000.
2
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Qualitative detection of hepatitis C virus RNA: comparison of analytical sensitivity, clinical performance, and workflow of the Cobas Amplicor HCV test version 2.0 and the HCV RNA transcription-mediated amplification qualitative assay.丙型肝炎病毒RNA的定性检测:Cobas Amplicor HCV检测试剂盒2.0版与HCV RNA转录介导的扩增定性检测方法的分析灵敏度、临床性能及工作流程比较
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Prospective multicenter clinical evaluation of AMPLICOR and COBAS AMPLICOR hepatitis C virus tests.AMPLICOR和COBAS AMPLICOR丙型肝炎病毒检测的前瞻性多中心临床评估。
J Clin Microbiol. 2001 Nov;39(11):4005-12. doi: 10.1128/JCM.39.11.4005-4012.2001.

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Clinical application of hepatitis C virus genotyping and quantitation.丙型肝炎病毒基因分型与定量的临床应用
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Serum levels of hepatitis C virus RNA predict non-response to interferon therapy: comparison of two commercial assays.丙型肝炎病毒RNA血清水平可预测对干扰素治疗无反应:两种商业检测方法的比较
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Is an "a la carte" combination interferon alfa-2b plus ribavirin regimen possible for the first line treatment in patients with chronic hepatitis C? The ALGOVIRC Project Group.对于丙型肝炎患者的一线治疗,采用“点菜式”组合的干扰素α-2b加利巴韦林方案是否可行?ALGOVIRC项目组。
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A comparison of reverse transcription-polymerase chain reaction and branched-chain DNA assays for hepatitis C virus RNA in patients receiving interferon treatment. Consensus Interferon Study Group.接受干扰素治疗患者丙型肝炎病毒RNA的逆转录-聚合酶链反应与分支DNA检测法的比较。共识干扰素研究小组。
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Genotype dependence of hepatitis C virus load measurement in commercially available quantitative assays.市售定量检测中丙型肝炎病毒载量测量的基因型依赖性
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Hepatitis C and liver transplantation.丙型肝炎与肝移植
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EASL International Consensus Conference on Hepatitis C. Paris, 26-28, February 1999, Consensus Statement. European Association for the Study of the Liver.欧洲肝脏研究协会丙型肝炎国际共识会议。巴黎,1999年2月26 - 28日,共识声明。
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Establishment of the first international standard for nucleic acid amplification technology (NAT) assays for HCV RNA. WHO Collaborative Study Group.首个丙型肝炎病毒核糖核酸(HCV RNA)核酸扩增技术(NAT)检测国际标准的制定。世界卫生组织协作研究小组。
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Comparative study of a modified competitive RT-PCR and Amplicor HCV monitor assays for quantitation of hepatitis C virus RNA in serum.改良竞争性逆转录聚合酶链反应与Amplicor HCV监测检测法对血清中丙型肝炎病毒RNA定量的比较研究
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丙型肝炎病毒RNA的改进版2.0定性和定量AMPLICOR逆转录-聚合酶链反应检测:国际单位校准、增强的基因型反应性及性能特征

Improved version 2.0 qualitative and quantitative AMPLICOR reverse transcription-PCR tests for hepatitis C virus RNA: calibration to international units, enhanced genotype reactivity, and performance characteristics.

作者信息

Lee S C, Antony A, Lee N, Leibow J, Yang J Q, Soviero S, Gutekunst K, Rosenstraus M

机构信息

Roche Molecular Systems, Inc., Pleasanton, California, USA.

出版信息

J Clin Microbiol. 2000 Nov;38(11):4171-9. doi: 10.1128/JCM.38.11.4171-4179.2000.

DOI:10.1128/JCM.38.11.4171-4179.2000
PMID:11060086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC87559/
Abstract

Version 2.0 qualitative and quantitative AMPLICOR reverse transcription-PCR tests for HCV were designed to improve on the performance of first version of the hepatitis C virus (HCV) tests. The new tests were calibrated in international units, the new commonly accepted standard unit of measurement for HCV RNA. The sensitivity of the qualitative tests was enhanced by modifying the specimen processing procedure to achieve a limit of detection 50 IU/ml. The limit of detection for the quantitative tests was 600 IU/ml. Modifications to the amplification reaction mixture and thermal cycling conditions enabled all genotypes to be amplified with similar efficiency. The quantitative tests exhibited a linear range extending from 500 to 500,000 IU/ml and excellent reproducibility, with coefficients of variation ranging from 18 to 39%, within the linear range. These data indicate that the version 2. 0 AMPLICOR HCV tests will improve diagnosis of HCV infection and will yield more-accurate titers for prognosis and for monitoring therapeutic efficacy, particularly at low viral loads. Furthermore, it will be possible to compare the performance characteristics and viral load measurements of AMPLICOR tests to those of other tests that adopt the international unit as the standard of measurement.

摘要

HCV的2.0版定性和定量AMPLICOR逆转录 - PCR检测旨在改进丙型肝炎病毒(HCV)检测第一版的性能。新检测以国际单位进行校准,这是HCV RNA新的普遍接受的标准测量单位。通过修改样本处理程序,定性检测的灵敏度得到提高,实现了50 IU/ml的检测限。定量检测的检测限为600 IU/ml。对扩增反应混合物和热循环条件的修改使所有基因型都能以相似的效率进行扩增。定量检测的线性范围从500到500,000 IU/ml,并且具有出色的重现性,在线性范围内变异系数为18%至39%。这些数据表明,2.0版AMPLICOR HCV检测将改善HCV感染的诊断,并将为预后和监测治疗效果产生更准确的滴度,特别是在低病毒载量时。此外,将有可能将AMPLICOR检测的性能特征和病毒载量测量结果与采用国际单位作为测量标准的其他检测进行比较。