Palmer Sarah, Wiegand Ann P, Maldarelli Frank, Bazmi Holly, Mican JoAnn M, Polis Michael, Dewar Robin L, Planta Angeline, Liu Shuying, Metcalf Julia A, Mellors John W, Coffin John M
HIV Drug Resistance Program, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702-1201, USA.
J Clin Microbiol. 2003 Oct;41(10):4531-6. doi: 10.1128/JCM.41.10.4531-4536.2003.
More sensitive assays for human immunodeficiency virus type 1 (HIV-1) RNA are needed to detect, quantify, and characterize persistent viremia in patients who are receiving antiretroviral therapy and whose plasma HIV-1 RNA levels are suppressed to less than 50 to 75 copies/ml. We therefore developed an internally controlled real-time reverse transcriptase-initiated PCR assay that quantifies HIV-1 RNA concentrations down to 1 copy per ml of plasma. This assay with single-copy sensitivity (the single-copy assay) generates a reproducible linear regression plot of input copy number versus threshold cycle by using HIV-1 RNA transcripts at copy numbers ranging from 1 to 10(6) per reaction mixture. The single-copy assay was compared to the ultrasensitive AMPLICOR HIV-1 MONITOR assay and a more sensitive modification of the ultrasensitive assay by repeatedly testing a low-copy-number panel containing 200 to 0.781 copies of HIV-1 RNA per ml of plasma. This comparison showed that the single-copy assay had a greater sensitivity than the other assays and was the only assay that detected HIV-1 RNA at levels as low as 0.781 copies/ml. Testing of plasma samples from 15 patients who were receiving antiretroviral therapy and who had <75 HIV-1 RNA copies/ml revealed persistent viremia in all 15 patients, with HIV-1 RNA levels ranging from 1 to 32 copies/ml (median, 13 copies/ml). The greater sensitivity of the single-copy assay should allow better characterization of persistent viremia in patients who are receiving antiretroviral therapy and whose HIV-1 RNA levels are suppressed to below the detection limits of present assays.
需要更灵敏的检测方法来检测、定量和表征接受抗逆转录病毒治疗且血浆人类免疫缺陷病毒1型(HIV-1)RNA水平被抑制至低于50至75拷贝/毫升的患者中的持续性病毒血症。因此,我们开发了一种内部对照实时逆转录引发的聚合酶链反应检测方法,该方法可将HIV-1 RNA浓度定量至每毫升血浆1拷贝。这种具有单拷贝灵敏度的检测方法(单拷贝检测法)通过使用每个反应混合物中拷贝数范围为1至10⁶的HIV-1 RNA转录本,生成输入拷贝数与阈值循环的可重复线性回归图。通过反复检测每毫升血浆中含有200至0.781拷贝HIV-1 RNA的低拷贝数样本组,将单拷贝检测法与超灵敏的AMPLICOR HIV-1 MONITOR检测法以及该超灵敏检测法的更灵敏改进方法进行了比较。该比较表明,单拷贝检测法比其他检测法具有更高的灵敏度,并且是唯一能检测到低至0.781拷贝/毫升水平的HIV-1 RNA的检测法。对15名接受抗逆转录病毒治疗且HIV-1 RNA拷贝数<75/毫升的患者的血浆样本进行检测,发现所有15名患者均存在持续性病毒血症,HIV-1 RNA水平范围为1至32拷贝/毫升(中位数为13拷贝/毫升)。单拷贝检测法更高的灵敏度应能更好地表征接受抗逆转录病毒治疗且HIV-1 RNA水平被抑制至当前检测法检测限以下的患者中的持续性病毒血症。