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Pulmonary infection induces persistent, pathogen-specific lipidomic changes influencing trained immunity
Lydia M Roberts1, Benjamin Schwarz1, Emily Speranza2,3
1Immunity to Pulmonary Pathogens Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Disease, National Institutes of Health, 903 S. 4th Street, Hamilton, MT 59840, USA.
Innate immunity develops memory after infection, a process influenced by host lipids. This study reveals how lung lipid changes impact the trained immune response to subsequent infections.
Area of Science:
- Immunology
- Metabolism
- Infectious Disease
Background:
- Infection resolution can induce trained innate immunity, enhancing defense against secondary infections.
- Epigenetic modifications, driven by host metabolism, are key to trained immunity.
- The role of lipids in trained immunity remains largely unexplored.
Purpose of the Study:
- To investigate the influence of lipids on the development and function of trained innate immunity.
- To identify pathogen-specific lipid alterations in the lung following bacterial infection.
- To understand how these lipid changes affect the trained immune response.
Main Methods:
- Utilized two models of pulmonary bacterial infection.
- Employed multi-omic approaches to analyze host response.
- Investigated changes in the lung lipidome and cellular populations.
Main Results:
- Identified persistent, pathogen-specific changes in the lung lipidome after infection.
- Observed correlations between lung lipidome alterations and trained immune responses.
- Characterized specific lung cell populations contributing to the altered lipidome.
Conclusions:
- Host lipids play a significant role in shaping the trained innate immune response.
- Pathogen-induced changes in the lung lipidome can inform subsequent immune defenses.
- This research deepens the understanding of pulmonary trained immunity and lipid metabolism.
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