Abstract

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.

Keywords

VirologyTiterVirusViral loadLiterBiologyPolymerase chain reactionLentivirusViral diseaseRNAHuman immunodeficiency virus (HIV)Real-time polymerase chain reactionGeneGenetics

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Year
1993
Type
article
Volume
259
Issue
5102
Pages
1749-1754
Citations
1238
Access
Closed

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M. Piatak, M. S. Saag, Linghui Yang et al. (1993). High Levels of HIV-1 in Plasma During All Stages of Infection Determined By Competitive PCR. Science , 259 (5102) , 1749-1754. https://doi.org/10.1126/science.8096089

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DOI
10.1126/science.8096089