Piatak M, Saag M S, Yang L C, Clark S J, Kappes J C, Luk K C, Hahn B H, Shaw G M, Lifson J D
Division of HIV and Exploratory Research, Genelabs Technologies Inc., Redwood City, CA 94063.
Science. 1993 Mar 19;259(5102):1749-54. doi: 10.1126/science.8096089.
Quantitative competitive polymerase chain reaction (QC-PCR) methods were used to quantify virion-associated human immunodeficiency virus type-1 (HIV-1) RNA in plasma from 66 patients with Centers for Disease Control stage I to IVC1 infection. HIV-1 RNA, ranging from 100 to nearly 22,000,000 copies per milliliter of plasma (corresponding to 50 to 11,000,000 virions per milliliter), was readily quantified in all subjects, was significantly associated with disease stage and CD4+ T cell counts, and decreased by as much as 235-fold with resolution of primary infection or institution of antiretroviral therapy. Plasma virus levels determined by QC-PCR correlated with, but exceeded by an average of 60,000-fold, virus titers measured by endpoint dilution culture. Quantitation of HIV-1 in plasma by QC-PCR may be useful in assessing the efficacy of antiretroviral agents, especially in early stage disease when conventional viral markers are often negative.
采用定量竞争性聚合酶链反应(QC-PCR)方法对66例疾病控制中心I至IVC1期感染的患者血浆中与病毒体相关的人类免疫缺陷病毒1型(HIV-1)RNA进行定量。所有受试者血浆中的HIV-1 RNA均易于定量,范围为每毫升血浆100至近22000000拷贝(相当于每毫升50至11000000个病毒体),与疾病分期和CD4+T细胞计数显著相关,并且随着原发性感染的消退或抗逆转录病毒治疗的开始,其水平下降多达235倍。通过QC-PCR测定的血浆病毒水平与终点稀释培养法测定的病毒滴度相关,但平均超出60000倍。通过QC-PCR对血浆中的HIV-1进行定量,可能有助于评估抗逆转录病毒药物的疗效,尤其是在疾病早期,此时传统病毒标志物往往为阴性。