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Respiratory Epithelial Memory: Uncovering the role of trained immunity in the respiratory epithelium

Project description

Immune memory in the lungs

The immune system comprises two main branches. The adaptive immune system mounts targeted responses and retains memory of past infections, while the innate immune system provides rapid, non-specific defence. Innate immunity was long thought to lack memory, but emerging evidence suggests that innate immune cells can undergo lasting functional changes after infection, a phenomenon called trained immunity. Whether respiratory epithelial cells, the first barrier encountered by airborne pathogens, can acquire similar memory remains poorly understood. With the support of the Marie Skłodowska-Curie Actions programme, the REMEMORY project investigates trained immunity in human airway epithelium using physiologically relevant in vitro models. By characterising metabolic, epigenomic and proteomic changes, the project aims to reveal novel therapeutic targets for preventing and treating respiratory infections.

Objective

Immunological memory, once thought to be exclusive to the adaptive immune system, is now increasingly recognized as a feature of innate immunity. This phenomenon, known as trained immunity, enables innate immune cells to undergo lasting functional changes after an initial infection, improving their response to future immune challenges. While trained immunity is well characterized in some cell types, its role in non-immune cells such as epithelium remains understudied. Respiratory epithelium is a major site of pathogen exposure, and recent studies hint at the ability for respiratory epithelial cells to undergo trained immunity. This project will provide a comprehensive analysis of trained immunity in the respiratory epithelium using a physiologically relevant in vitro model of human airway epithelium. An interdisciplinary approach will be used to characterize metabolic, epigenomic, transcriptomic, and proteomic changes associated with the trained phenotype. Functional relevance will be assessed through viral challenge experiments, and findings will be validated using clinical respiratory cell samples collected after viral infection. Altogether, this work will expand the understanding of trained immunity in barrier tissues and may reveal novel therapeutic targets for preventing and treating respiratory infections.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

(opens in new window) HORIZON-MSCA-2025-PF

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Coordinator

UNIVERSITE LYON 1 CLAUDE BERNARD
Net EU contribution
€ 226 420,56
Address
BOULEVARD DU 11 NOVEMBRE 1918 NUM43
69622 Villeurbanne Cedex
France
Region
Auvergne-Rhône-Alpes Rhône-Alpes Rhône
Activity type
Higher or Secondary Education Establishments
Links
Total cost
No data