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首页> 外文期刊>Journal of Clinical Microbiology >Japanese Reference Panel of Blood Specimens for Evaluation of Hepatitis C Virus RNA and Core Antigen Quantitative Assays
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Japanese Reference Panel of Blood Specimens for Evaluation of Hepatitis C Virus RNA and Core Antigen Quantitative Assays

机译:日本参考血液标本小组评估丙型肝炎病毒RNA和核心抗原定量分析

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摘要

An accurate and reliable quantitative assay for hepatitis C virus (HCV) is essential for measuring viral propagation and the efficacy of antiviral therapy. There is a growing need for domestic reference panels for evaluation of clinical assay kits because the performance of these kits may vary with region-specific genotypes or polymorphisms. In this study, we established a reference panel by selecting 80 donated blood specimens in Japan that tested positive for HCV. Using this panel, we quantified HCV viral loads using two HCV RNA kits and five core antigen (Ag) kits currently available in Japan. The data from the two HCV RNA assay kits showed excellent correlation. All RNA titers were distributed evenly across a range from 3 to 7 log IU/ml. Although the data from the five core Ag kits also correlated with RNA titers, the sensitivities of individual kits were not sufficient to quantify viral load in all samples. As calculated by the correlation with RNA titers, the theoretical lower limits of detection by these core Ag assays were higher than those for the detection of RNA. Moreover, in several samples in our panel, core Ag levels were underestimated compared to RNA titers. Sequence analysis in the HCV core region suggested that polymorphisms at amino acids 47 to 49 of the core Ag were responsible for this underestimation. The panel established in this study will be useful for estimating the quality of currently available and upcoming HCV assay kits; such quality control is essential for clinical usage of these kits.
机译:准确可靠的丙型肝炎病毒(HCV)定量测定对于测量病毒繁殖和抗病毒治疗的疗效至关重要。越来越需要用于临床分析试剂盒的国内参考专家组,因为这些试剂盒的性能可能随区域特定的基因型或多态性而变化。在这项研究中,我们通过选择80个在日本检测出HCV呈阳性的献血标本建立了一个参考小组。使用该面板,我们使用目前在日本可获得的两种HCV RNA试剂盒和五种核心抗原(Ag)试剂盒对HCV病毒载量进行了定量。来自两种HCV RNA分析试剂盒的数据显示出极好的相关性。所有RNA滴度均匀分布在3至7 log IU / ml的范围内。尽管来自五个核心Ag试剂盒的数据也与RNA滴度相关,但单个试剂盒的敏感性不足以量化所有样品中的病毒载量。通过与RNA滴度的相关性计算得出,这些核心Ag测定的理论下限高于检测RNA的下限。此外,在我们小组的几个样品中,与RNA滴度相比,核心Ag水平被低估了。 HCV核心区域的序列分析表明,核心Ag的氨基酸47至49处的多态性导致了这种低估。这项研究中建立的小组将有助于评估目前可用和即将到来的HCV检测试剂盒的质量;这种质量控制对于这些试剂盒的临床使用至关重要。

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