Switch to maraviroc/raltegravir dual therapy leads to an unfavorable immune profile with low-level HIV viremia

AIDS. 2015 Apr 24;29(7):853-6. doi: 10.1097/QAD.0000000000000626.

Abstract

Immunovirological consequences of a switch to a maraviroc/raltegravir dual therapy were analyzed in 16 HIV-infected patients with persistent viral load below 50 copies/ml. At 26-week postswitch, the CD4/CD8 ratio decreased and the CD8 T-cell activation increased. A decrease in classical monocytes was associated with a shift toward a proinflammatory monocyte profile and negatively correlated with ultrasensitive viral load. Thus, this therapeutic switch induced a proinflammatory profile probably driven by a slight loss of virus control.

Publication types

  • Clinical Study

MeSH terms

  • Anti-HIV Agents / therapeutic use*
  • CD4-CD8 Ratio
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Cyclohexanes / therapeutic use*
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / immunology*
  • Humans
  • Lymphocyte Activation
  • Male
  • Maraviroc
  • Middle Aged
  • Monocytes / immunology
  • RNA, Viral / blood
  • Raltegravir Potassium / therapeutic use*
  • Treatment Outcome
  • Triazoles / therapeutic use*
  • Viral Load*
  • Viremia*

Substances

  • Anti-HIV Agents
  • Cyclohexanes
  • RNA, Viral
  • Triazoles
  • Raltegravir Potassium
  • Maraviroc