Plasma Biomarkers of Human Immunodeficiency Virus-Related Systemic Inflammation and Immune Activation in Sub-Saharan Africa Before and During Suppressive Antiretroviral Therapy

J Infect Dis. 2019 Aug 9;220(6):1029-1033. doi: 10.1093/infdis/jiz252.

Abstract

We evaluated immune biomarker profiles in human immunodeficiency virus (HIV)-infected adults (n = 398) from 5 African countries. Although all biomarkers decreased after antiretroviral therapy (ART) initiation, levels of C-X-C chemokine ligand 10 (CXCL10), lipopolysaccharide-binding protein, C-reactive protein, soluble CD163, and soluble scavenger receptor CD14 were significantly higher during ART than in an HIV-uninfected reference group (n = 90), indicating persistent monocyte/macrophage activation, inflammation, and microbial translocation. Before ART initiation, high HIV viral load was associated with elevated CXCL10 and tuberculosis coinfection was associated with elevated soluble CD14. High pre-ART levels of each biomarker strongly predicted residual immune activation during ART. Chemokine (C-C motif) ligand 2, lipopolysaccharide-binding protein, C-reactive protein, and interleukin 6 were differentially expressed between countries. Further research is needed on the clinical implications of residual immune dysregulation.

Keywords: HIV; antiretroviral therapy; biomarkers; immune activation; inflammation; sub-Saharan Africa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins
  • Adult
  • Africa South of the Sahara
  • Anti-HIV Agents / therapeutic use*
  • Antigens, CD / blood*
  • Antigens, Differentiation, Myelomonocytic / blood*
  • Biomarkers / blood
  • C-Reactive Protein / analysis*
  • CD4 Lymphocyte Count
  • Carrier Proteins / blood*
  • Chemokine CCL2 / blood*
  • Chemokine CXCL10 / blood*
  • Cohort Studies
  • Coinfection / drug therapy
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / immunology
  • HIV Infections / virology
  • HIV-1 / drug effects
  • HIV-1 / immunology*
  • Humans
  • Inflammation / blood
  • Inflammation / immunology
  • Interleukin-6 / blood*
  • Lipopolysaccharide Receptors / blood*
  • Male
  • Membrane Glycoproteins / blood*
  • Receptors, Cell Surface / blood*
  • Tuberculosis / drug therapy
  • Viral Load / drug effects

Substances

  • Acute-Phase Proteins
  • Anti-HIV Agents
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CCL2 protein, human
  • CD14 protein, human
  • CD163 antigen
  • CXCL10 protein, human
  • Carrier Proteins
  • Chemokine CCL2
  • Chemokine CXCL10
  • IL6 protein, human
  • Interleukin-6
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • lipopolysaccharide-binding protein
  • C-Reactive Protein