...
首页> 外文期刊>Journal of Clinical Microbiology >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
【24h】

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

机译:改进的2.0版定性和定量AMPLICOR逆转录PCR检测丙型肝炎病毒RNA:国际单位校准,增强的基因型反应性和性能特征

获取原文
   

获取外文期刊封面封底 >>

       

摘要

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.
机译:设计用于HCV的2.0版定性和定量AMPLICOR逆转录PCR实验,以提高第一版丙型肝炎病毒(HCV)测试的性能。新的测试以国际单位进行校准,HCV RNA是国际上公认的新的标准测量单位。通过修改样品处理程序以达到50 IU / ml的检出限,可以提高定性测试的灵敏度。定量测试的检出限为600 IU / ml。对扩增反应混合物和热循环条件的修改使得所有基因型都能以相似的效率被扩增。定量测试的线性范围从500到500,000 IU / ml,再现性极佳,线性范围内的变异系数在18%到39%之间。这些数据表明2.0版AMPLICOR HCV测试将改善HCV感染的诊断,并产生更准确的滴度用于预后和监测治疗效果,尤其是在低病毒载量下。此外,有可能将AMPLICOR测试的性能特征和病毒载量测量与采用国际单位作为测量标准的其他测试进行比较。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号