S'abonner

Regulation of plasma soluble receptors of TNF and IL-1 in patients with COVID-19 differs from that observed in sepsis - 06/12/24

Doi : 10.1016/j.jinf.2024.106300 
Muhammed D. Aksu a, b, Tijmen van der Ent a, Zhenhua Zhang c, d, Anca L. Riza e, f, Aline H. de Nooijer a, Isis Ricaño-Ponce a, Nico Janssen a, Job J. Engel a, Ioana Streata e, f, Helga Dijkstra a, Heidi Lemmers a, Inge Grondman a, Valerie A.C.M. Koeken a, c, d, g, Eleni Antoniadou h, Nikolaos Antonakos i, Frank L. van de Veerdonk a, Yang Li a, c, d, Evangelos J. Giamarellos-Bourboulis i, Mihai G. Netea a, j, Athanasios Ziogas a,
a Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands 
b Department of Basic Oncology, Hacettepe University Cancer Institute, Ankara, Turkey 
c Department of Computational Biology of Individualised Medicine, Centre for Individualised Infection Medicine (CiiM), a Joint Venture Between the Hannover Medical School and the Helmholtz Centre for Infection Research, Hannover, Lower Saxony, Germany 
d TWINCORE, Centre for Experimental and Clinical Infection Research, a Joint Venture Between the Hannover Medical School and the Helmholtz Centre for Infection Research, Hannover, Lower Saxony, Germany 
e Human Genomics Laboratory, University of Medicine and Pharmacy of Craiova, Romania 
f Regional Centre of Medical Genetics Dolj, County Clinical Emergency Hospital Craiova, Romania 
g Research Centre Innovations in Care, Rotterdam University of Applied Sciences, Rotterdam, the Netherlands 
h Intensive Care Unit, “G. Gennimatas” Hospital, Thessaloniki, Greece 
i 4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece 
j Department for Genomics and Immunoregulation, Life and Medical Sciences Institute (LIMES), University of Bonn, Bonn, Germany 

Correspondence to: Department of Internal Medicine (463), Geert Grooteplein Zuid 10, 6525 GA Nijmegen, the Netherlands.Department of Internal Medicine (463)Geert Grooteplein Zuid 10Nijmegen6525 GAthe Netherlands

Bienvenue sur EM-consulte, la référence des professionnels de santé.
Article gratuit.

Connectez-vous pour en bénéficier!

Summary

Objectives

IL-1α/β and TNF are closely linked to the pathology of severe COVID-19 and sepsis. The soluble forms of their receptors, functioning as decoy receptors, exhibit inhibitory effects. However, little is known about their regulation in severe bacterial and viral infections, which we aimed to investigate in this study.

Methods

The circulating soluble receptors of TNF (sTNFR1 and sTNFR2) and IL-1α/β (sIL-1R1, sIL-1R2) were evaluated in the plasma of patients with COVID-19, severe bacterial infections, and sepsis and compared with healthy controls. Additionally, IL1R1, IL1R2, TNFRSF1A, and TNFRSF1B expression was evaluated at the single cell level in PBMCs derived from COVID-19 or sepsis patients.

Results

Plasma concentrations of sIL-1R1, sTNFR1, and sTNFR2 were significantly higher in COVID-19 patients compared to healthy subjects. Notably, sIL-1R1 levels were particularly elevated in ICU COVID-19 patients, and transcriptome analysis indicated heightened IL1R1 expression in PBMCs from severe COVID-19 patients. In severe bacterial infections, only sTNFR1 and sTNFR2 exhibited increased levels compared to healthy controls. Sepsis patients had decreased sIL-1R1 plasma concentrations but elevated sIL-1R2, sTNFR1, and sTNFR2 levels compared to healthy individuals, reflecting the heightened expression due to the increased numbers of monocytes present in sepsis. Finally, elevated concentrations of sIL-1R2, sTNFR1, and sTNFR2 were moderately associated with reduced 28-day survival in sepsis patients.

Conclusion

Our study reveals distinct regulation of plasma concentrations of soluble IL-1 receptors in COVID-19 and sepsis. Moreover, soluble TNF receptors 1 and 2 consistently rise in all conditions and show a positive correlation with disease severity in sepsis.

Le texte complet de cet article est disponible en PDF.

Highlights

sIL-1R1 plasma concentrations were elevated in COVID-19 patients.
sIL-1R2 but not sIL-1R1 plasma concentrations were elevated in sepsis patients.
Plasma sTNFR1 and sTNFR2 were elevated in both COVID-19 and sepsis patients.
Transcriptional regulation varied across PBMC subpopulations in COVID-19 and sepsis.
sIL-1R2, sTNFR1, and sTNFR2 were associated with increased severity in sepsis.

Le texte complet de cet article est disponible en PDF.

Abbreviations : ADAM17, AUC, APACHE-II, ARDS, BMI, CCI, CI, CO-RADS, COVID-19, CRP, CT, CV, DC, DEG, EDTA, ELISA, GCP, ICU, IL-1, IL-1R1, IL-1R2, IL-1RA, IL-1RacP, mDC, MODS, N/A, NK, PBMCs, pDC, ROC, RT-PCR, SARS-CoV-2, SD, SOFA, scRNA-seq, sIL-1R1, sIL-1R2, SIRS, TIR, sTNFR1, sTNFR2, TNF, TNFR1, TNFR2, UMAP

Keywords : COVID-19, Sepsis, STNFR1, STNFR2, SIL-1R1, SIL-1R2


Plan


© 2024  The Author(s). Publié par Elsevier Masson SAS. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 89 - N° 6

Article 106300- décembre 2024 Retour au numéro
Article précédent Article précédent
  • Recurrent Clostridioides difficile infections in solid organ transplant recipients: The international CALIPSO study
  • Giusy Tiseo, Dafna Yahav, Alaa Atamna, Tomer Avni, Manuel Causse, Elena Pérez-Nadales, Alessandra Mularoni, Elena Reigadas, María Olmedo-Samperio, Mario Fernández-Ruiz, Zaira R. Palacios-Baena, Jesus Rodríguez-Baño, Paolo De Simone, Giandomenico Biancofiore, Eman Fares Sabik, Mical Paul, José María Aguado, Ugo Boggi, Patricia Muñoz, Julián Torres-Cisneros, Alessio Farcomeni, Marco Falcone, ESCMID Study Group for Infections in the Elderly (ESGIE)
| Article suivant Article suivant
  • Modelling multiplex testing for outbreak control
  • Martyn Fyles, Christopher E. Overton, Thomas Ward, Emma Bennett, Tom Fowler, Ian Hall

Bienvenue sur EM-consulte, la référence des professionnels de santé.

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2025 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.