Pneumococcal conjugate vaccine modulates macrophage-mediated innate immunity in pneumonia caused by Streptococcus pneumoniae following influenza.
Animals
Antibodies, Bacterial
/ blood
B7-2 Antigen
/ metabolism
Bacterial Load
Coinfection
/ immunology
Cytokines
/ metabolism
Disease Models, Animal
Immunity, Innate
Influenza A virus
Lung
/ immunology
Macrophages
/ immunology
Mice
Neutrophils
/ immunology
Orthomyxoviridae Infections
/ immunology
Phagocytosis
Pneumococcal Vaccines
/ administration & dosage
Pneumonia, Pneumococcal
/ immunology
Streptococcus pneumoniae
Survival Rate
Vaccination
Vaccines, Conjugate
/ administration & dosage
Influenza virus infection
Innate immunity
Monocyte/macrophages
Pneumococcal colonization
Pneumococcal conjugate vaccine
Secondary pneumococcal pneumonia
Journal
Microbes and infection
ISSN: 1769-714X
Titre abrégé: Microbes Infect
Pays: France
ID NLM: 100883508
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
05
09
2019
revised:
09
12
2019
accepted:
10
12
2019
pubmed:
21
1
2020
medline:
3
6
2021
entrez:
21
1
2020
Statut:
ppublish
Résumé
Pneumococcal conjugate vaccination (PCV) may prevent influenza-related pneumonia, including Streptococcus pneumoniae pneumonia. To investigate PCV efficacy against secondary pneumococcal pneumonia following influenza, PCV was administered intramuscularly 2 and 5 weeks before S. pneumoniae serotype-3 colonization of murine nasopharynges followed by intranasal challenge with a sublethal dose of influenza A virus. Bacterial and viral loads, including innate immune responses were compared across conditions. PCV vaccination improved the survival of mice with secondary pneumococcal pneumonia and significantly reduced the pulmonary bacterial burden. Increased monocyte/macrophage influx into the lungs, alleviated loss of alveolar macrophages and decreased neutrophil influx into the lungs occurred in PCV-treated mice irrespective of pneumococcal colonization. Higher monocyte chemoattractant protein 1 levels and lower levels of CXCL1, interferon-γ, interleukin-17A, and IL-10, were detected in PCV-treated mice. Additionally, PCV treatment activated the macrophage intracellular killing of S. pneumoniae. Collectively, PCV potentially modulates the host's innate immunity and specific antibodies induction. Macrophage-related innate immunity should be further explored to elucidate the efficacy and mechanisms of PCV versus influenza-related life-threatening diseases.
Identifiants
pubmed: 31958572
pii: S1286-4579(20)30008-3
doi: 10.1016/j.micinf.2019.12.005
pii:
doi:
Substances chimiques
Antibodies, Bacterial
0
B7-2 Antigen
0
Cytokines
0
Pneumococcal Vaccines
0
Vaccines, Conjugate
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
312-321Informations de copyright
Copyright © 2020 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare no competing interests.