TY - JOUR
T1 - Severe COVID-19 induces prolonged elevation of the acute-phase protein pentraxin 3
AU - Kratzer, Bernhard
AU - Stieger, Robert B
AU - Durmus, Seyma
AU - Trapin, Doris
AU - Gattinger, Pia
AU - Ettel, Paul
AU - Sehgal, Al Nasar Ahmed
AU - Borochova, Kristina
AU - Dorofeeva, Yulia
AU - Tulaeva, Inna
AU - Grabmeier-Pfistershammer, Katharina
AU - Tauber, Peter A
AU - Gerdov, Marika
AU - Perkmann, Thomas
AU - Fae, Ingrid
AU - Wenda, Sabine
AU - Kundi, Michael
AU - Wrighton, Sebastian
AU - Fischer, Gottfried F
AU - Valenta, Rudolf
AU - Pickl, Winfried F
N1 - Publisher Copyright:
Copyright © 2025 Kratzer, Stieger, Durmus, Trapin, Gattinger, Ettel, Sehgal, Borochova, Dorofeeva, Tulaeva, Grabmeier-Pfistershammer, Tauber, Gerdov, Perkmann, Fae, Wenda, Kundi, Wrighton, Fischer, Valenta and Pickl.
PY - 2025/10
Y1 - 2025/10
N2 - 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.
AB - 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.
KW - Humans
KW - C-Reactive Protein/genetics
KW - COVID-19/blood
KW - Serum Amyloid P-Component/genetics
KW - Male
KW - Female
KW - Middle Aged
KW - SARS-CoV-2
KW - Adult
KW - Aged
KW - Severity of Illness Index
KW - Biomarkers/blood
KW - Polymorphism, Single Nucleotide
KW - pentraxin-3
KW - acute-phase proteins
KW - COVID-19
KW - severe COVID-19
KW - soluble pattern recognition receptors
UR - https://www.scopus.com/pages/publications/105019032801
U2 - 10.3389/fimmu.2025.1672485
DO - 10.3389/fimmu.2025.1672485
M3 - Journal article
C2 - 41103408
SN - 1664-3224
VL - 16
SP - 1672485
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1672485
ER -