Enhanced expression of the CXCR4 co-receptor in HIV-1-infected individualscorrelates with the emergence of syncytia-inducing strains

The aim of this study was to investigate the mechanisms responsible for the emergence in some HIV-1-infected individuals of highly aggressive, syncyti a-inducing (SI) HIV-1 strains, which have been shown to use CXCR4 as corece ptor to enter target cells. To this end, the percentages of circulating CXC R4(+)CD4(+) T cells were evaluated by flow cytometry in 39 untreated and 61 highly active antiretroviral therapy (HAART)-treated HIV-1-infected indivi duals in comparison with 35 HIV-1 seronegative subjects. Plasma viremia was also measured, and HIV primary Isolates, from both untreated and HAART-tre ated HIV-1-infected subjects, were tested for the presence of SI strains. T he results of this study showed enhanced proportions of CXCR4(+)CD4(+) T ce lls in untreated patients in comparison with HAART-treated and healthy subj ects. Furthermore, the results of a 12-month longitudinal study in a cohort of 11 patients undergoing HAART showed a significant reduction of CXCR4 ex pression after successful therapy. Finally, a significant positive correlat ion among the proportions of circulating CXCR4-expressing CD4(+) T cells, p lasma viremia, and the probability to isolate Si strains was found. These i n vivo data are in keeping with previous in vitro results suggesting a bidi rectional link between HIV-1 and CXCR4 expression on CD4(+) T cells, and pr ovide some clues to understanding the mechanisms exerting a selective press ure toward the emergence of SI strains.