Evolution of Serum Acute-Phase Glycoproteins Assessed by 1H-NMR in HIV Elite Controllers

Front Immunol. 2021 Sep 28:12:730691. doi: 10.3389/fimmu.2021.730691. eCollection 2021.

Abstract

Elite controllers (ECs) are an exceptional group of people living with HIV (PLWH) who maintain undetectable viral loads (VLs) despite not being on antiretroviral therapy (ART). However, this phenotype is heterogeneous, with some of these subjects losing virological control over time. In this longitudinal retrospective study, serum acute-phase glycoprotein profile assessed by proton nuclear magnetic resonance (1H-NMR) was determined in 11 transient controllers (TCs) who spontaneously lost virological control and 11 persistent controllers (PCs) who persistently maintained virological control over time. Both PCs and TCs showed similar acute-phase glycoprotein profiles, even when TCs lost the virological control (GlycB, p = 0.824 and GlycA, p = 0.710), and the serum acute-phase glycoprotein signature in PCs did not differ from that in HIV-negative subjects (GlycB, p = 0.151 and GlycA, p = 0.243). Differences in serum glycoproteins A and B were significant only in ECs compared to HIV-typical progressors (TPs) with < 100 CD4+ T-cells (p < 0.001). 1H-NMR acute-phase glycoprotein profile does not distinguish TCs form PCs before the loss of viral control. ECs maintain a low-grade inflammatory state compared to TPs. PCs revealed a closer serum signature to HIV-negative subjects, reaffirming this phenotype as a closer model of functional control of HIV.

Keywords: HIV; acute-phase glycoproteins; elite controllers; inflammation; proton nuclear magnetic resonance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / metabolism*
  • Adult
  • Biomarkers / blood
  • Female
  • Glycomics*
  • HIV / pathogenicity*
  • HIV Infections / blood*
  • HIV Infections / diagnosis
  • HIV Non-Progressors*
  • Host-Pathogen Interactions
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Prognosis
  • Proteome*
  • Proteomics*
  • Proton Magnetic Resonance Spectroscopy*
  • Retrospective Studies
  • Time Factors

Substances

  • Acute-Phase Proteins
  • Biomarkers
  • Proteome