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Corticosteroid and antimicrobial therapy in macrolide-resistant pneumococcal pneumonia porcine model

  • Ana Motos
  • , Minlan Yang
  • , Denise Battaglini
  • , Hua Yang
  • , Andrea Meli
  • , Joaquim Bobi
  • , Roberto Cabrera
  • , Giacomo Tanzella
  • , Carmen Rosa Vargas
  • , Marta Arrieta
  • , Blanca Llonch
  • , Nona Rovira-Ribalta
  • , Enric Barbeta
  • , Pierluigi di Giannatale
  • , Stefano Nogas
  • , Laia Fernández-Barat
  • , Montserrat Rigol
  • , Kasra Kiarostami
  • , Ignacio Martín-Loeches
  • , Jordi Vila
  • Daniel Martinez, Gianluigi Li Bassi, Antoni Torres*
*Corresponding author for this work
  • Hospital Clinic de Barcelona
  • August Pi i Sunyer Biomedical Research Institute
  • University of Barcelona
  • Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES)
  • Nantes Université
  • Capital Medical University
  • San Martino Hospital Genoa
  • University of Milan
  • SS Annunziata Hospital
  • St. James’s Hospital
  • Barcelona Institute for Global Health (ISGlobal)
  • Centro de Investigación Biomédica En Red- Enfermedades Infecciosas (CIBERINFEC)
  • Prince Charles Hospital
  • University of Queensland
  • Queensland University of Technology
  • The Wesley Research Institute

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
95 Downloads (Pure)

Abstract

Background: 

Streptococcus pneumoniae, a primary cause of community-acquired pneumonia (CAP), is typically treated with β-lactams and macrolides or quinolones. Corticosteroids are now recommended as adjunctive therapy in severe CAP to improve outcomes. In this prospective randomized animal study, we evaluated the bactericidal efficacy of various antibiotic regimens combined with corticosteroids using a porcine pneumococcal pneumonia model. 

Results: 

In 30 White-Landrace female pigs, pneumonia was induced by intrabronchial inoculation of macrolide-resistant S. pneumoniae 19A isolate. Animals were randomized to receive saline, ceftriaxone (CRO) with levofloxacin (LVX), CRO with azithromycin (AZM), or combinations of these with methylprednisolone (MP). The primary outcome, S. pneumoniae concentrations in lung tissue after 48 h of treatment, showed that the CRO + LVX, CRO + AZM, CRO + LVX + MP, and CRO + AZM + MP groups were equally effective in reducing bacterial load. However, complete bacterial eradication from lung tissue was achieved only in the CRO + AZM + MP group. Secondary outcomes, including bacterial burden in tracheal aspirates and bronchoalveolar lavage (BAL) samples, showed similar bactericidal activity across all treatment groups. The CRO + AZM + MP group demonstrated the most controlled inflammatory response, achieving baseline levels of inflammation, while other groups exhibited elevated inflammatory markers. 

Conclusions: 

Despite using a macrolide-resistant S. pneumoniae isolate, the combination of CRO, AZM, and MP achieves similar or even superior results compared to other antibiotic combinations. This regimen provides both bactericidal and immunomodulatory benefits, suggesting its effectiveness in treating macrolide-resistant S. pneumoniae pneumonia.

Original languageEnglish
Article number27
JournalIntensive Care Medicine Experimental
Volume13
Issue number1
DOIs
Publication statusPublished - 27 Feb 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

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