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Antibiotic use during influenza infection augments lung eosinophils that impair immunity against secondary bacterial pneumonia.
Sanches Santos Rizzo Zuttion, Marilia; Parimon, Tanyalak; Bora, Stephanie A; Yao, Changfu; Lagree, Katherine; Gao, Catherine A; Wunderink, Richard G; Kitsios, Georgios D; Morris, Alison; Zhang, Yingze; McVerry, Bryan J; Modes, Matthew E; Marchevsky, Alberto M; Stripp, Barry R; Soto, Christopher M; Wang, Ying; Merene, Kimberly; Cho, Silvia; Victor, Blandine L; Vujkovic-Cvijin, Ivan; Gupta, Suman; Cassel, Suzanne; Sutterwala, Fayyaz S; Devkota, Suzanne; Underhill, David M; Chen, Peter.
Afiliación
  • Sanches Santos Rizzo Zuttion M; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Parimon T; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Bora SA; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Yao C; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Lagree K; Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Gao CA; Division of Pulmonary and Critical Care, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, United States of America.
  • Wunderink RG; Division of Pulmonary and Critical Care, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, United States of America.
  • Kitsios GD; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Pittsburgh, Pittsburgh, United States of America.
  • Morris A; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Pittsburgh, Pittsburgh, United States of America.
  • Zhang Y; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Pittsburgh, Pittsburgh, United States of America.
  • McVerry BJ; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Pittsburgh, Pittsburgh, United States of America.
  • Modes ME; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Marchevsky AM; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Stripp BR; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Soto CM; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Wang Y; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Merene K; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Cho S; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Victor BL; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Vujkovic-Cvijin I; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Gupta S; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Cassel S; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Sutterwala FS; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Devkota S; Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Underhill DM; Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, United States of America.
  • Chen P; Women's Guild Lung Institute, Cedars-Sinai Medical Center, Los Angeles, United States of America.
J Clin Invest ; 2024 Sep 10.
Article en En | MEDLINE | ID: mdl-39255040
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 antibiotic treatment during influenza infection causes a fungal dysbiosis that drive lung eosinophilia and impair MRSA clearance. Finally, we evaluated three cohorts of hospitalized patients and found 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Invest / J. clin. invest / Journal of clinical investigation Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Invest / J. clin. invest / Journal of clinical investigation Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos