Lee S C, Antony A, Lee N, Leibow J, Yang J Q, Soviero S, Gutekunst K, Rosenstraus M
Roche Molecular Systems, Inc., Pleasanton, California, USA.
J Clin Microbiol. 2000 Nov;38(11):4171-9. doi: 10.1128/JCM.38.11.4171-4179.2000.
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.
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。