The cytokines HGF and CXCL13 predict the severity and the mortality in COVID-19 patients.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
09 08 2021
Historique:
received: 14 02 2021
accepted: 15 07 2021
entrez: 10 8 2021
pubmed: 11 8 2021
medline: 18 8 2021
Statut: epublish

Résumé

The objective of the present study was to identify biological signatures of severe coronavirus disease 2019 (COVID-19) predictive of admission in the intensive care unit (ICU). Over 170 immunological markers were investigated in a 'discovery' cohort (n = 98 patients) of the Lausanne University Hospital (LUH-1). Here we report that 13 out of 49 cytokines were significantly associated with ICU admission in the three cohorts (P < 0.05 to P < 0.001), while cellular immunological markers lacked power in discriminating between ICU and non-ICU patients. The cytokine results were confirmed in two 'validation' cohorts, i.e. the French COVID-19 Study (FCS; n = 62) and a second LUH-2 cohort (n = 47). The combination of hepatocyte growth factor (HGF) and C-X-C motif chemokine ligand 13 (CXCL13) was the best predictor of ICU admission (positive and negative predictive values ranging from 81.8% to 93.1% and 85.2% to 94.4% in the 3 cohorts) and occurrence of death during patient follow-up (8.8 fold higher likelihood of death when both cytokines were increased). Of note, HGF is a pleiotropic cytokine with anti-inflammatory properties playing a fundamental role in lung tissue repair, and CXCL13, a pro-inflammatory chemokine associated with pulmonary fibrosis and regulating the maturation of B cell response. Up-regulation of HGF reflects the most powerful counter-regulatory mechanism of the host immune response to antagonize the pro-inflammatory cytokines including CXCL13 and to prevent lung fibrosis in COVID-19 patients.

Identifiants

pubmed: 34373466
doi: 10.1038/s41467-021-25191-5
pii: 10.1038/s41467-021-25191-5
pmc: PMC8352963
doi:

Substances chimiques

Biomarkers 0
CXCL13 protein, human 0
Chemokine CXCL13 0
Cytokines 0
HGF protein, human 0
Hepatocyte Growth Factor 67256-21-7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4888

Informations de copyright

© 2021. The Author(s).

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Auteurs

Matthieu Perreau (M)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Madeleine Suffiotti (M)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Pedro Marques-Vidal (P)

Service of Internal Medicine, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Aurelie Wiedemann (A)

Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France.
Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d'Immunologie Clinique, Créteil, France.

Yves Levy (Y)

Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France.
Assistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, Service d'Immunologie Clinique, Créteil, France.

Cédric Laouénan (C)

AP-HP, Hôpital Bichat, Département Épidémiologie Biostatistiques et Recherche Clinique, INSERM, Centre d'Investigation clinique-Epidémiologie Clinique 1425, Paris, France.
Université de Paris, INSERM, IAME UMR 1137, Paris, France.

Jade Ghosn (J)

AP-HP, Hôpital Bichat, Service de Maladies Infectieuses et Tropicales, Paris, France.

Craig Fenwick (C)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Denis Comte (D)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Thierry Roger (T)

Service of Infectious Diseases, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Jean Regina (J)

Service of Infectious Diseases, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Peter Vollenweider (P)

Service of Internal Medicine, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Gerard Waeber (G)

Service of Internal Medicine, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Mauro Oddo (M)

Service of Intensive Care, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Thierry Calandra (T)

Service of Infectious Diseases, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Giuseppe Pantaleo (G)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland. Giuseppe.Pantaleo@chuv.ch.
Vaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France. Giuseppe.Pantaleo@chuv.ch.
Swiss Vaccine Research Institute, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland. Giuseppe.Pantaleo@chuv.ch.

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