Neutrophils-related host factors associated with severe disease and fatality in patients with influenza infection.
Cell Cycle
/ immunology
Extracellular Traps
/ immunology
Female
Gene Expression
/ genetics
Humans
Influenza A Virus, H1N1 Subtype
/ immunology
Influenza A Virus, H3N2 Subtype
/ immunology
Influenza B virus
/ immunology
Influenza, Human
/ immunology
Lung
/ immunology
Male
Middle Aged
Neutrophil Activation
/ immunology
Neutrophils
/ immunology
Prospective Studies
Respiration, Artificial
Respiratory Insufficiency
/ mortality
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
31 07 2019
31 07 2019
Historique:
received:
22
10
2018
accepted:
28
06
2019
entrez:
2
8
2019
pubmed:
2
8
2019
medline:
18
12
2019
Statut:
epublish
Résumé
Severe influenza infection has no effective treatment available. One of the key barriers to developing host-directed therapy is a lack of reliable prognostic factors needed to guide such therapy. Here, we use a network analysis approach to identify host factors associated with severe influenza and fatal outcome. In influenza patients with moderate-to-severe diseases, we uncover a complex landscape of immunological pathways, with the main changes occurring in pathways related to circulating neutrophils. Patients with severe disease display excessive neutrophil extracellular traps formation, neutrophil-inflammation and delayed apoptosis, all of which have been associated with fatal outcome in animal models. Excessive neutrophil activation correlates with worsening oxygenation impairment and predicted fatal outcome (AUROC 0.817-0.898). These findings provide new evidence that neutrophil-dominated host response is associated with poor outcomes. Measuring neutrophil-related changes may improve risk stratification and patient selection, a critical first step in developing host-directed immune therapy.
Identifiants
pubmed: 31366921
doi: 10.1038/s41467-019-11249-y
pii: 10.1038/s41467-019-11249-y
pmc: PMC6668409
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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