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首页> 外文期刊>Journal of Clinical Microbiology >New Real-Time Reverse Transcriptase-Initiated PCR Assay with Single-Copy Sensitivity for Human Immunodeficiency Virus Type 1 RNA in Plasma
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New Real-Time Reverse Transcriptase-Initiated PCR Assay with Single-Copy Sensitivity for Human Immunodeficiency Virus Type 1 RNA in Plasma

机译:对血浆中人免疫缺陷病毒1型RNA具有单拷贝敏感性的新型实时逆转录酶起始PCR分析

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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 106 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.
机译:需要更灵敏的1型人类免疫缺陷病毒(HIV-1)RNA检测方法,以检测,定量和表征接受抗逆转录病毒疗法且血浆HIV-1 RNA水平被抑制至小于50至75拷贝的患者的持续病毒血症/毫升。因此,我们开发了一种内部控制的实时逆转录酶引发的PCR测定法,该测定法可将HIV-1 RNA的浓度降低至每毫升血浆1个拷贝。这种具有单拷贝敏感性的测定法(单拷贝测定法)使用HIV-1 RNA转录本,其拷贝数范围为1至10 6 ,生成了输入拷贝数与阈值循环的可再现线性回归图。每个反应混合物。通过重复测试每毫升血浆中含有200至0.781拷贝HIV-1 RNA的低拷贝数面板,将单拷贝测定与超灵敏AMPLICOR HIV-1 MONITOR测定和超灵敏测定的更灵敏修饰进行了比较。该比较表明,单拷贝测定法比其他测定法具有更高的灵敏度,并且是唯一检测到低至0.781拷贝/ ml的HIV-1 RNA的测定法。对15例接受抗逆转录病毒治疗且血浆<75 HIV-1 RNA拷贝/毫升的患者的血浆样品进行测试后发现,所有15例患者均存在持续病毒血症,HIV-1 RNA的水平范围为1至32拷贝/毫升(中位数,13份数/毫升)。单拷贝测定法的更高灵敏度应该可以更好地表征正在接受抗逆转录病毒疗法并且其HIV-1 RNA水平被抑制到当前测定法检测限以下的患者的持续病毒血症。

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