Severe COVID-19 induces prolonged elevation of the acute-phase protein pentraxin 3

  • Bernhard Kratzer
  • , Robert B Stieger
  • , Seyma Durmus
  • , Doris Trapin
  • , Pia Gattinger
  • , Paul Ettel
  • , Al Nasar Ahmed Sehgal
  • , Kristina Borochova
  • , Yulia Dorofeeva
  • , Inna Tulaeva
  • , Katharina Grabmeier-Pfistershammer
  • , Peter A Tauber
  • , Marika Gerdov
  • , Thomas Perkmann
  • , Ingrid Fae
  • , Sabine Wenda
  • , Michael Kundi
  • , Sebastian Wrighton
  • , Gottfried F Fischer
  • , Rudolf Valenta
  • Winfried F Pickl

Research output: Journal article (peer-reviewed)Journal article

Abstract

Introduction: During the acute-phase of COVID-19, elevated levels of several acute-phase proteins, such as C-reactive protein (CRP), mannose-binding lectin (MBL), pentraxin 3 (PTX-3), serum amyloid A (SAA) and surfactant protein D (SP-D), are associated with severe to fatal clinical outcomes. Typically, these markers return to baseline within days after resolution of the acute infection. Methods: In this study, we assessed the plasma levels of these proteins in a well-defined cohort of 141 COVID-19 convalescent patients 10 weeks after infection and compared them to 98 non-infected controls. In addition, we performed genetic analyses in a subgroup of patients and related the findings with structural equation modelling to disease severity. Results: In contrast to other acute-phase proteins, PTX-3 levels were significantly higher in severe COVID-19 convalescent patients than in the control group. Furthermore, a higher proportion of patients with severe COVID-19 exhibited PTX-3 levels above 5000 pg/ml even 10 months post-infection, compared to those with mild disease. To explore potential genetic influences, a genetic analysis was performed on all severely affected patients (n=36) and on an age- and sex-matched subset of mild COVID-19 patients (n=38). Results revealed a significantly higher frequency (p<0.0001) of the homozygous wildtype genotype of the PTX-3 SNP rs971145291 in severe (15 out of 36) versus mild (1 out of 38) COVID-19 patients. Using structural equation modelling, the association of this PTX-3 genotype and disease severity was shown to be mediated by elevated PTX-3 levels, with no contribution from other analyzed (clinical) confounders. Discussion: In summary, severe COVID-19 patients show high PTX-3 serum levels which may be influenced by genetic predisposition, specifically the absence of the rs971145291 SNP variant. PTX-3 may thus serve both as a biomarker for tissue damage and/or long-term immune activation and eventually post-COVID-19 complications.

Original languageEnglish
Article number1672485
Pages (from-to)1672485
JournalFrontiers in Immunology
Volume16
DOIs
Publication statusPublished - Oct 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Humans
  • C-Reactive Protein/genetics
  • COVID-19/blood
  • Serum Amyloid P-Component/genetics
  • Male
  • Female
  • Middle Aged
  • SARS-CoV-2
  • Adult
  • Aged
  • Severity of Illness Index
  • Biomarkers/blood
  • Polymorphism, Single Nucleotide
  • pentraxin-3
  • acute-phase proteins
  • COVID-19
  • severe COVID-19
  • soluble pattern recognition receptors

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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