CD14+CD16+ monocyte transmigration across the blood-brain barrier is associated with HIV-NCI despite viral suppression

JCI Insight. 2024 Sep 10;9(17):e179855. doi: 10.1172/jci.insight.179855.

Abstract

HIV-associated neurocognitive impairment (HIV-NCI) affects 15%-50% of people with HIV (PWH), despite viral suppression with antiretroviral therapy (ART). HIV neuropathogenesis is mediated, in part, by transmigration of infected CD14+CD16+ monocytes across the blood-brain barrier (BBB) into the central nervous system (CNS). In the CNS, CD14+CD16+ monocytes contribute to infection and activation of parenchymal cells, resulting in production of neurotoxic viral and host factors that cause neuronal damage. Mechanisms by which CD14+CD16+ monocytes contribute to HIV-NCI have not been characterized in a study population of PWH on ART without contribution from confounders that affect cognition (e.g., substance use, hepatitis C virus coinfection). We assessed cognitive function, PBMC transmigration across the BBB, and neuronal health markers in a well-defined cohort of 56 PWH on ART using stringent criteria to eliminate confounding factors. We demonstrated that PWH on ART with HIV-NCI have significantly increased transmigration of their CD14+CD16+ monocytes across the BBB compared with those with normal cognition. We showed that hypertension and diabetes may be effect modifiers on the association between CD14+CD16+ monocyte transmigration and cognition. This study underscored the persistent role of CD14+CD16+ monocytes in HIV-NCI, even in PWH with viral suppression, suggesting them as potential targets for therapeutic interventions.

Keywords: AIDS/HIV; Cell migration/adhesion; Monocytes.

MeSH terms

  • AIDS Dementia Complex / immunology
  • AIDS Dementia Complex / metabolism
  • Adult
  • Blood-Brain Barrier* / metabolism
  • Female
  • GPI-Linked Proteins / metabolism
  • HIV Infections* / drug therapy
  • HIV Infections* / immunology
  • HIV Infections* / metabolism
  • HIV Infections* / virology
  • Humans
  • Lipopolysaccharide Receptors* / metabolism
  • Male
  • Middle Aged
  • Monocytes* / immunology
  • Monocytes* / metabolism
  • Receptors, IgG* / metabolism

Substances

  • Receptors, IgG
  • Lipopolysaccharide Receptors
  • FCGR3B protein, human
  • CD14 protein, human
  • GPI-Linked Proteins