HIV-1 viral DNA load in peripheral blood mononuclear cells from seroconverters and long-term infected individuals

Abstract

Objective To determine viral DNA load in peripheral blood mononuclear cells (PBMC) from HIV-1-infected individuals. Design HIV-1 copy numbers were determined using a quantitative polymerase chain reaction (PCR), the PCR-aided template titration assay (PATTY). PATTY utilizes an internal plasmid control DNA, which is amplified within the same tube and using the same primers as the PBMC target DNA. HIV-1 copy numbers were confirmed by limiting-dilution PCR analysis. Results PBMC viral load of 19 long-term (>4 years) HIV-1-infected individuals ranged from 0.8 to 100 copies per 10³ PBMC. Significantly higher copy numbers were found among p24-antigen-positive than among p24-antigen-negative individuals. In addition, the PBMC viral load of two HIV-1-infected individuals was monitored during the first 3 months after acute infection. For both patients, the HIV-1 copy numbers were shown to peak at the time of HIV-1-antibody seroconversion and decline subsequently (range, 0.6–10 copies per 10³ PBMC). Conclusions ATTY is a useful method for assessing the HIV-1 copy numbers in PBMC DNA. Viral DNA load peaks shortly after infection and reaches an individual specific level that is probably stable within a few months of infection. Viral DNA load in PBMC varies widely among long-term HIV-1-infected individuals.