4.6 Article

Infrequent HIV Infection of Circulating Monocytes during Antiretroviral Therapy

Journal

JOURNAL OF VIROLOGY
Volume 94, Issue 1, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.01174-19

Keywords

HIV reservoir; integrated HIV DNA; monocytes

Categories

Funding

  1. Canadian Institutes for Health Research (CIHR) [364408]
  2. Canadian HIV Cure Enterprise Team Grant from the CIHR [HIG-133050]
  3. CANFAR
  4. IAS
  5. Reseau SIDA et Maladies Infectieuses du Fonds de Recherche du Quebec-Sante (FRQS)
  6. amfAR [109316]
  7. FAIR
  8. U.S. National Institutes of Health [R01-NS061696]
  9. BP-DGR AGAUR Postdoctoral Fellowship
  10. Research Scholar Career Award of the Quebec Health Research Fund (FRQ-S) [253292]

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Whereas human immunodeficiency virus (HIV) persists in tissue macrophages during antiretroviral therapy (ART), the role of circulating monocytes as HIV reservoirs remains controversial. Three magnetic bead selection methods and flow cytometry cell sorting were compared for their capacity to yield pure CD14(+) monocyte populations. Cell sorting by flow cytometry provided the purest population of monocytes (median CD4(+) T-cell contamination, 0.06%), and the levels of CD4(+) T-cell contamination were positively correlated with the levels of integrated HIV DNA in the monocyte populations. Using cell sorting by flow cytometry, we assessed longitudinally the infection of monocytes and other cell subsets in a cohort of 29 Thai HIV-infected individuals. Low levels of HIV DNA were detected in a minority of monocyte fractions obtained before and after 1 year of ART (27% and 33%, respectively), whereas HIV DNA was readily detected in CD4(+) T cells from all samples. Additional samples (2 to 5 years of ART) were obtained from 5 individuals in whom monocyte infection was previously detected. Whereas CD4(+) T cells were infected at high levels at all time points, monocyte infection was inconsistent and absent in at least one longitudinal sample from 4/5 individuals. Our results indicate that infection of monocytes is infrequent and highlight the importance of using flow cytometry cell sorting to minimize contamination by CD4(+) T cells. IMPORTANCE The role of circulating monocytes as persistent HIV reservoirs during ART is still controversial. Several studies have reported persistent infection of monocytes in virally suppressed individuals; however, others failed to detect HIV in this subset. These discrepancies are likely explained by the diversity of the methods used to isolate monocytes and to detect HIV infection. In this study, we show that only flow cytometry cell sorting yields a highly pure population of monocytes largely devoid of CD4 contaminants. Using this approach in a longitudinal cohort of HIV-infected individuals before and during ART, we demonstrate that HIV is rarely found in monocytes from untreated and treated HIV-infected individuals. This study highlights the importance of using methods that yield highly pure populations of cells as flow cytometry cell sorting to minimize and control for CD4(+) T-cell contamination.

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