In vivo effect of two first-line ART regimens on inflammatory mediators in male HIV patients

Lipids Health Dis. 2014 May 29:13:90. doi: 10.1186/1476-511X-13-90.

Abstract

Background: Persistent immune activation and inflammation are lying behind HIV-infection even in the setting of ART mediated viral suppression. The purpose of this study is to define the in vivo effect of two first-line ART regimens on certain inflammatory mediators in male HIV patients.

Methods: Male, naive, HIV-infected volunteers were assigned either to tenofovir-DF/emtricitabine/efavirenz (Group_T) or abacavir/lamivudine/efavirenz (Group_A). Platelet Activating Factor (PAF) levels and metabolic enzymes together with HIV-implicated cytokines (IL-1beta, IL-6, IL-8, IL-10, IL-12p70, TNFa) and VEGF were determined for a 12-month period. Differences within each group were determined by non-parametric Friedman and Wilcoxon test, while the differences between the groups were checked by ANOVA repeated measures.

Results: Both ART regimens present pronounced effect on inflammatory mediators, resulting in decreased PAF levels and Lipoprotein-associated phospholipase A2 (Lp-PLA2) activity for tenofovir-containing regimen and same as baseline PAF levels with a peak though at the 3rd month as well as elevated Lp-PLA2 activity for abacavir-containing regimen.

Conclusions: Studies regarding the effect of first-line ART regimens on inflammation may be beneficial in preventing chronic morbidities during HIV-treatment. From this point of view, the present study suggests an anti-inflammatory effect of tenofovir-containing ART, while the temporary increase of PAF levels in abacavir-containing ART may be the link between the reported cardiovascular risk and abacavir administration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Adult
  • Alkynes
  • Animals
  • Anti-HIV Agents / therapeutic use*
  • Benzoxazines / therapeutic use
  • Cyclopropanes
  • HIV Infections / drug therapy*
  • HIV Infections / metabolism*
  • Humans
  • Interleukin-10 / metabolism
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Lamivudine / therapeutic use
  • Male
  • Middle Aged
  • Organophosphonates / therapeutic use
  • Platelet Activating Factor / metabolism
  • Tenofovir
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Alkynes
  • Anti-HIV Agents
  • Benzoxazines
  • Cyclopropanes
  • Interleukin-6
  • Interleukin-8
  • Organophosphonates
  • Platelet Activating Factor
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Lamivudine
  • Tenofovir
  • Adenine
  • efavirenz