Ehret Robert, Harb Kudor, Breuer Stefan, Obermeier Martin
Medical Center for Infectious Diseases, Berlin, Germany.
Medical Center for Infectious Diseases, Berlin, Germany.
J Clin Virol. 2022 Apr;149:105127. doi: 10.1016/j.jcv.2022.105127. Epub 2022 Mar 9.
HIV-1 RNA quantification is a key component of treatment monitoring.
To assess the performance of a redesigned HIV-1 RNA quantitative assay that uses a dual-target approach: Xpert® HIV-1 Viral Load (VL) XC.
Fresh and frozen samples (N = 533) from HIV-1 positive patients tested with Abbott HIV-1 assays (Alinity m and RealTime [m2000]) were retested using the new Xpert XC assay. Three samples with known underquantification using the previous single-target Xpert assay were retested.
The Xpert XC assay yielded valid results in 98.5% (N = 528/536) of cases and showed high sensitivity in 80 fresh samples that had undetectable VLs or ≤1.7 log copies/mL with Alinity m. Linear regression and Bland-Altman analyses showed high concordance with the Abbott tests for quantified samples over a wide VL range (1.6-6.9 copies/mL), including non-B subtypes (mean difference=-0.1±0.23 log copies/mL). Mutations associated with integrase resistance did not impact the results. Very good linearity and reproducibility was shown for the tested subtypes B, CRF06_cpx, and CRF02_AG. Xpert XC VLs in samples that were previously underquantified using the original single-target Xpert assay were similar to those detected by the Abbott assays (±0.11 log copies/mL).
The Xpert XC assay showed excellent correlation with the Abbott assays for all tested HIV-1 subtypes. Sensitivity, linearity and accuracy were high in the therapeutically relevant VL range. With a time to result of only 90 min, this on-demand decentralized assay is a safe, reliable and fast option for VL monitoring in HIV-1-infected patients.
HIV-1 RNA定量是治疗监测的关键组成部分。
评估一种重新设计的采用双靶点方法的HIV-1 RNA定量检测方法:Xpert® HIV-1病毒载量(VL)XC的性能。
使用雅培HIV-1检测方法(Alinity m和RealTime [m2000])检测的HIV-1阳性患者的新鲜和冷冻样本(N = 533),采用新的Xpert XC检测方法进行重新检测。对之前使用单靶点Xpert检测方法已知定量不足的3个样本进行重新检测。
Xpert XC检测方法在98.5%(N = 528/536)的病例中产生了有效的结果,并且在80个使用Alinity m检测病毒载量不可检测或≤1.7 log拷贝/mL的新鲜样本中显示出高灵敏度。线性回归和Bland-Altman分析表明,在较宽的病毒载量范围(1.6 - 6.9拷贝/mL)内,包括非B亚型,与雅培检测方法对定量样本具有高度一致性(平均差异 = -0.1±0.23 log拷贝/mL)。与整合酶耐药相关的突变不影响结果。对于测试的B亚型、CRF06_cpx和CRF02_AG亚型,显示出非常好的线性和可重复性。之前使用原始单靶点Xpert检测方法定量不足的样本中的Xpert XC病毒载量与雅培检测方法检测到的病毒载量相似(±0.11 log拷贝/mL)。
Xpert XC检测方法在所有测试的HIV-1亚型中与雅培检测方法显示出极好的相关性。在治疗相关的病毒载量范围内,灵敏度、线性和准确性都很高。由于出结果时间仅为90分钟,这种按需分散式检测方法是HIV-1感染患者病毒载量监测的一种安全、可靠且快速的选择。