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Updated: Dec 31, 2025

Isolation and In Vitro Culture of Murine and Human Alveolar Macrophages
Published on: April 20, 2018
Influenza-induced monocyte-derived alveolar macrophages confer prolonged antibacterial protection
Helena Aegerter1, Justina Kulikauskaite1, Stefania Crotta1
1Immunoregulation Laboratory, Francis Crick Institute, London, UK.
Abstract:
Despite the prevalence and clinical importance of influenza, its long-term effect on lung immunity is unclear. Here we describe that following viral clearance and clinical recovery, at 1 month after infection with influenza, mice are better protected from Streptococcus pneumoniae infection due to a population of monocyte-derived alveolar macrophages (AMs) that produce increased interleukin-6. Influenza-induced monocyte-derived AMs have a surface phenotype similar to resident AMs but display a unique functional, transcriptional and epigenetic profile that is distinct from resident AMs. In contrast, influenza-experienced resident AMs remain largely similar to naive AMs. Thus, influenza changes the composition of the AM population to provide prolonged antibacterial protection. Monocyte-derived AMs persist over time but lose their protective profile. Our results help to understand how transient respiratory infections, a common occurrence in human life, can constantly alter lung immunity by contributing monocyte-derived, recruited cells to the AM population.
Insights
Influenza infection enhances lung antibacterial immunity for a month by recruiting new alveolar macrophages (AMs). These monocyte-derived AMs produce interleukin-6, offering protection that wanes over time.
Area of Science:
- Immunology
- Respiratory Medicine
- Microbiology
Background:
- Influenza's long-term impact on lung immunity remains poorly understood.
- Understanding post-infection immune dynamics is crucial for managing secondary bacterial infections.
Purpose of the Study:
- To investigate the long-term effects of influenza infection on lung immunity and host defense.
- To characterize the immune cells responsible for altered protection after influenza recovery.
Main Methods:
- Murine model of influenza infection followed by Streptococcus pneumoniae challenge.
- Flow cytometry and transcriptomic analysis to phenotype and functionally assess alveolar macrophages (AMs).
- Epigenetic profiling of AM subsets.
Main Results:
- One month post-influenza, mice exhibited enhanced protection against Streptococcus pneumoniae.
- This protection was mediated by a distinct population of monocyte-derived AMs producing increased interleukin-6.
- Influenza-induced AMs possessed unique functional, transcriptional, and epigenetic profiles compared to resident AMs.
Conclusions:
- Influenza infection alters lung immune cell composition, promoting a protective AM population.
- Monocyte-derived AMs contribute to prolonged, but transient, antibacterial defense.
- Transient respiratory infections continuously shape lung immunity through recruitment of new immune cells.
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