AI Article Synopsis

  • Cytomegalovirus (CMV) infection is prevalent among individuals with HIV, and its effects on CD4+ and CD8+ T cells following cART (combination antiretroviral therapy) initiation are not fully understood.
  • A study from the French Dat'AIDS cohort included 503 patients who achieved HIV suppression, finding that 88.3% were CMV seropositive (CMV+), which correlated negatively with the CD4:CD8 T cell ratio.
  • The research suggests that CMV+ status may hinder normal T cell ratios, hinting at faster T cell aging, which calls for closer monitoring and evaluation of the potential benefits of treating asymptomatic CMV co-infections in HIV patients.

Article Abstract

Cytomegalovirus (CMV) infection is common among HIV-infected patients but its repercussion on the course of CD4+ and CD8+ T cells after cART initiation remains elusive. The French Dat'AIDS cohort enrolled 5,688 patients on first-line cART, from which we selected patients who achieved HIV suppression for at least 12 months without modification of cART, and for whom CMV serostatus was available. Five hundred and three patients fulfilled the selection criteria (74% male, median age 43 yrs, 15.5% CDC stage C), of whom 444 (88.3%) were seropositive for CMV (CMV+). Multivariate analyses using mixed-linear models adjusted for the time from HIV suppression, sex, age, transmission risk group, duration of HIV follow-up, the interaction between time from HIV suppression and CMV+ serology, and the nadir CD4 count revealed a negative correlation between CMV+ and CD4:CD8 ratio (coeff. = -0.16; p = 0.001). This correlation was also observed among patients displaying optimal CD4 recovery (≥500 cells/mm3 at M12; coeff. = -0.24; p = 0.002). Hence, CMV+ serostatus antagonizes normalization of the CD4:CD8 ratio, although further analyses of the impact of co-morbidities that associate with CMV serostatus, like HCV infection, are needed to elucidate this antagonism formally. However, this might reflect a premature T cell senescence, thus advocating for a close monitoring of T cells in CMV co-infected patients. In addition, our results raise the question of the benefit of treatment for asymptomatic CMV co-infection in HIV-infected patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100980PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0165774PLOS

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