CD177, a specific marker of neutrophil activation, is associated with coronavirus disease 2019 severity and death.
Details
Download: 34127958_BIB_909F730EC11C.pdf (4595.45 [Ko])
State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_909F730EC11C
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
CD177, a specific marker of neutrophil activation, is associated with coronavirus disease 2019 severity and death.
Journal
iScience
Working group(s)
French COVID cohort study group
ISSN
2589-0042 (Electronic)
ISSN-L
2589-0042
Publication state
Published
Issued date
23/07/2021
Peer-reviewed
Oui
Volume
24
Number
7
Pages
102711
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Abstract
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.
Keywords
immunology, virology
Pubmed
Web of science
Open Access
Yes
Create date
28/06/2021 10:59
Last modification date
09/08/2024 15:02