Yen-Lieberman B, Brambilla D, Jackson B, Bremer J, Coombs R, Cronin M, Herman S, Katzenstein D, Leung S, Lin H J, Palumbo P, Rasheed S, Todd J, Vahey M, Reichelderfer P
Cleveland Clinic Foundation, University Hospitals of Cleveland, Ohio, USA.
J Clin Microbiol. 1996 Nov;34(11):2695-701. doi: 10.1128/jcm.34.11.2695-2701.1996.
A number of quantitative assays have been developed by using amplification techniques to measure human immunodeficiency virus type 1 RNA in the plasma of infected individuals. The Virology Committee of the AIDS Clinical Trials Group in the Division of AIDS, National Institute of Allergy and Infectious Diseases, has established a quality assurance program (QAP) for quantitative assays of HIV-1 RNA levels in plasma. The primary objective of the QAP was to ascertain that a laboratory could maintain the precision required to have a 90% power to detect a fivefold difference in RNA copy number between two samples in the same batch. To achieve this goal, the QAP required an intra-assay standard deviation of no greater than 0.15 log10 RNA copies per ml. Panels for proficiency testing consisted of coded replicate samples and a common set of standards. To date, 41 laboratories have participated in the program and have used both commercial and in-house assays. We demonstrated that 65% of the laboratories were capable of attaining the necessary level of intra-assay precision. The fitted regressions indicated that the differences among laboratories that used the same kit were generally greater than the differences among population-average regressions for the kits themselves. The use of an external QAP and a common set of standards reduced differences both among laboratories that used the same kit and among laboratories that used different kits. Thus, use of a common set of standards across clinical trial protocols would allow for cross-protocol comparisons.
已经开发了许多定量测定方法,通过使用扩增技术来测量受感染个体血浆中的人类免疫缺陷病毒1型RNA。美国国立过敏与传染病研究所艾滋病司艾滋病临床试验组的病毒学委员会已经建立了一个血浆中HIV-1 RNA水平定量测定的质量保证计划(QAP)。QAP的主要目标是确定一个实验室能够维持所需的精密度,即有90%的把握检测同一批次中两个样本之间RNA拷贝数五倍的差异。为实现这一目标,QAP要求批内标准差不大于每毫升0.15 log10 RNA拷贝数。能力验证小组由编码重复样本和一组通用标准组成。到目前为止,已有41个实验室参与了该计划,并使用了商业检测方法和内部检测方法。我们证明,65%的实验室能够达到必要的批内精密度水平。拟合回归表明,使用相同试剂盒的实验室之间的差异通常大于试剂盒本身总体平均回归之间的差异。使用外部QAP和一组通用标准减少了使用相同试剂盒的实验室之间以及使用不同试剂盒的实验室之间的差异。因此,在临床试验方案中使用一组通用标准将允许进行跨方案比较。