CD177, a specific marker of neutrophil activation, is associated with coronavirus disease 2019 severity and death.
Détails
Télécharger: 34127958_BIB_909F730EC11C.pdf (4595.45 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
ID Serval
serval:BIB_909F730EC11C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
CD177, a specific marker of neutrophil activation, is associated with coronavirus disease 2019 severity and death.
Périodique
iScience
Collaborateur⸱rice⸱s
French COVID cohort study group
ISSN
2589-0042 (Electronic)
ISSN-L
2589-0042
Statut éditorial
Publié
Date de publication
23/07/2021
Peer-reviewed
Oui
Volume
24
Numéro
7
Pages
102711
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
The identification of patients with coronavirus disease 2019 and high risk of severe disease is a challenge in routine care. We performed cell phenotypic, serum, and RNA sequencing gene expression analyses in severe hospitalized patients (n = 61). Relative to healthy donors, results showed abnormalities of 27 cell populations and an elevation of 42 cytokines, neutrophil chemo-attractants, and inflammatory components in patients. Supervised and unsupervised analyses revealed a high abundance of CD177, a specific neutrophil activation marker, contributing to the clustering of severe patients. Gene abundance correlated with high serum levels of CD177 in severe patients. Higher levels were confirmed in a second cohort and in intensive care unit (ICU) than non-ICU patients (P < 0.001). Longitudinal measurements discriminated between patients with the worst prognosis, leading to death, and those who recovered (P = 0.01). These results highlight neutrophil activation as a hallmark of severe disease and CD177 assessment as a reliable prognostic marker for routine care.
Mots-clé
immunology, virology
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/06/2021 10:59
Dernière modification de la notice
09/08/2024 15:02