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Antibiotic use during influenza infection augments lung eosinophils that impair immunity against secondary bacterial pneumonia.

Authors :
Sanches Santos Rizzo Zuttion M
Parimon T
Bora SA
Yao C
Lagree K
Gao CA
Wunderink RG
Kitsios GD
Morris A
Zhang Y
McVerry BJ
Modes ME
Marchevsky AM
Stripp BR
Soto CM
Wang Y
Merene K
Cho S
Victor BL
Vujkovic-Cvijin I
Gupta S
Cassel SL
Sutterwala FS
Devkota S
Underhill DM
Chen P
Source :
The Journal of clinical investigation [J Clin Invest] 2024 Sep 10; Vol. 134 (21). Date of Electronic Publication: 2024 Sep 10.
Publication Year :
2024

Abstract

A leading cause of mortality after influenza infection is the development of a secondary bacterial pneumonia. In the absence of a bacterial superinfection, prescribing antibacterial therapies is not indicated but has become a common clinical practice for those presenting with a respiratory viral illness. In a murine model, we found that antibiotic use during influenza infection impaired the lung innate immunologic defenses toward a secondary challenge with methicillin-resistant Staphylococcus aureus (MRSA). Antibiotics augment lung eosinophils, which have inhibitory effects on macrophage function through the release of major basic protein. Moreover, we demonstrated that antibiotic treatment during influenza infection caused a fungal dysbiosis that drove lung eosinophilia and impaired MRSA clearance. Finally, we evaluated 3 cohorts of hospitalized patients and found that eosinophils positively correlated with antibiotic use, systemic inflammation, and worsened outcomes. Altogether, our work demonstrates a detrimental effect of antibiotic treatment during influenza infection that has harmful immunologic consequences via recruitment of eosinophils to the lungs, thereby increasing the risk of developing a secondary bacterial infection.

Details

Language :
English
ISSN :
1558-8238
Volume :
134
Issue :
21
Database :
MEDLINE
Journal :
The Journal of clinical investigation
Publication Type :
Academic Journal
Accession number :
39255040
Full Text :
https://doi.org/10.1172/JCI180986