Different biological significance of sCD14 and LPS in HIV-infection: importance of the immunovirology stage and association with HIV-disease progression markers

J Infect. 2012 Nov;65(5):431-8. doi: 10.1016/j.jinf.2012.06.008. Epub 2012 Jun 20.

Abstract

Objectives: Bacterial lipopolysaccharide (LPS) and soluble CD14 (sCD14) levels have been indistinctly used to measure bacterial translocation independently of the immunovirological stage in HIV infection; however, when the association of both markers with different HIV-progression end-points has been studied, discrepant results have been reported. The aim of this study was to assess the relationship between LPS and sCD14 in different HIV-infection immune stages and to determine the relationship between these biomarkers with established HIV-disease-progression-related markers, as T-cell immune activation, high-sensitivity C-reactive protein and D-dimer.

Methods: Seventy-three chronically HIV-1-infected patients with detectable HIV-1 RNA levels were analyzed. LPS levels by use of limulus lysate assay, sCD14, intestinal fatty acid binding protein and inflammation-coagulation-associated biomarkers were assessed.

Results: In this study, we found that LPS and sCD14 levels were only associated when low CD4+ T-cell levels and high HIV RNA levels were present. In addition, only sCD14 levels, but not LPS, were independently associated with HIV-disease progression-related markers, supporting the clinical importance of sCD14.

Conclusions: These results indicate that LPS and sCD14 have a different biological significance and should not be indistinctly used without taking the HIV immunovirological stage into account.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Bacterial Translocation
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • CD4 Lymphocyte Count
  • Disease Progression
  • Female
  • Fibrin Fibrinogen Degradation Products / metabolism
  • HIV Infections / blood*
  • HIV Infections / immunology*
  • HIV Infections / virology
  • Humans
  • Lipopolysaccharide Receptors / blood*
  • Lipopolysaccharides / blood*
  • Male
  • Middle Aged
  • RNA, Viral / blood
  • Statistics, Nonparametric
  • Viral Load

Substances

  • Biomarkers
  • Fibrin Fibrinogen Degradation Products
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • RNA, Viral
  • fibrin fragment D
  • C-Reactive Protein