Lillo Flavia B, Grasso Maria Angela, Lodini Sara, Bellotti Maria Grazia, Colucci Giuseppe
Laboratory of Virology, IRCCS Hospital San Raffaele, AIDS Center San Luigi, Via Stamira, D'Ancona 20, 20127 Milan, Italy.
J Virol Methods. 2004 Sep 15;120(2):201-5. doi: 10.1016/j.jviromet.2004.05.008.
Recent studies have suggested that monitoring the amount of HIV provirus in peripheral blood mononuclear cells (PBMCs) may be a useful end point for HAART where, in combination with plasma viral load, it provides additional information as to the possibility of virus eradication. In the present study, a modified version of the Cobas Amplicor HIV-1 Monitor test (CAHIM), currently used to quantify plasma viremia, have been evaluated to also measure the amount of proviral DNA in PBMCs. The analytical and clinical performance of the modified CAHIM test was assessed by quantifying different amounts of a standard HIV-DNA preparation obtained from the 8E5 cell line and by analysing 165 patients and controls samples. In these experiments, the modified test, that showed a linear dynamic range from 1.7 to 4.7 log10 copies/10(6) cells (r = 0.99) with a maximum CV of 20%, proved able to detect and quantify HIV-DNA in all but one clinical samples, with concentrations varying from 1.3 to 3.8 log10 copies/10(6) cells. During anti-retroviral treatment, the assay revealed different proviral DNA time courses associated with viral load changes and inversely correlated with CD4+ cells count. As expected, HIV-DNA was always detectable even when plasma viremia fell below the CAHIM cut-off. The modified CAHIM test specificity was confirmed by testing 20 HIV-negative samples in triplicates. Taken together, the data showed that the modified CAHIM test can be used to monitor HIV proviral DNA changes during HAART and can help in investigating further the clinical use of this marker.
近期研究表明,监测外周血单核细胞(PBMC)中HIV前病毒的数量可能是高效抗逆转录病毒治疗(HAART)的一个有用终点,它与血浆病毒载量相结合,可提供有关病毒根除可能性的额外信息。在本研究中,对目前用于定量血浆病毒血症的Cobas Amplicor HIV-1 Monitor检测(CAHIM)的改良版本进行了评估,以测量PBMC中前病毒DNA的数量。通过对从8E5细胞系获得的不同量标准HIV-DNA制剂进行定量,并分析165例患者和对照样本,评估了改良CAHIM检测的分析性能和临床性能。在这些实验中,改良检测显示线性动态范围为1.7至4.7 log10拷贝/10(6)细胞(r = 0.99),最大变异系数(CV)为20%,除一份临床样本外,能够检测和定量所有临床样本中的HIV-DNA,浓度范围为1.3至3.8 log10拷贝/10(6)细胞。在抗逆转录病毒治疗期间,该检测揭示了与病毒载量变化相关且与CD4+细胞计数呈负相关的不同前病毒DNA时间进程。正如预期的那样,即使血浆病毒血症降至CAHIM临界值以下,HIV-DNA也始终可检测到。通过对20份HIV阴性样本进行一式三份检测,证实了改良CAHIM检测的特异性。综上所述,数据表明改良CAHIM检测可用于监测HAART期间HIV前病毒DNA的变化,并有助于进一步研究该标志物的临床应用。