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

Marilia Sanches Santos Rizzo Zuttion, Tanyalak Parimon, Stephanie A. Bora, Changfu Yao, Katherine Lagree, Catherine A. Gao, Richard G. Wunderink, Georgios D. Kitsios, Alison Morris, Yingze Zhang, Bryan J. McVerry, Matthew E. Modes, Alberto M. Marchevsky, Barry R. Stripp, Christopher M. Soto, Ying Wang, Kimberly Merene, Silvia Cho, Blandine L. Victor, Ivan Vujkovic-CvijinSuman Gupta, Suzanne L. Cassel, Fayyaz S. Sutterwala, Suzanne Devkota, David M. Underhill, Peter Chen*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Article numbere180986
JournalJournal of Clinical Investigation
Volume134
Issue number21
DOIs
StatePublished - Nov 1 2024

Funding

Authorship note: MSSRZ, TP, and SAB contributed equally to this work. Conflict of interest: GDK has received research funding from Karius Inc. and Pfizer Inc. AM has received research funding from Pfizer Inc. BJMV has received consulting fees from Boehringer Ingelheim, BioAegis, and Synairgen Research Ltd. Copyright: \u00A9 2024, Sanches Santos Rizzo Zuttion et al. This is an open access article pub lished under the terms of the Creative Commons Attribution 4.0 International License. Submitted: March 12, 2024; Accepted: September 6, 2024; Published: September 10, 2024. Reference information: J Clin Invest. 2024;134(21):e180986. https://doi.org/10.1172/JCI180986. We appreciate help from the Flow Cytometry, Applied Genomics, Proteomics, and Research Informatics cores at Cedars-Sinai Medical Center. This work was supported by grants from the NIH (K08HL1411590 to TP; F32HL162377 to CAG; U19AI135964, U01TR003528, P01HL154998, R01HL14988, and R01LM013337 to RGW; R03HL162655 to GDK; R01HL163646 and R01HL164177 to AM; P01HL114453 to BJM; R01HL159953 and R01HL155759 to PC). This research was also supported by NIH National Center for Advancing Translational Sciences UCLA Clinical and Translational Science Institute grant UL1TR001881.

ASJC Scopus subject areas

  • General Medicine

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