Interleukin-22 regulates interferon lambda expression in a mice model of pseudomonas aeruginosa pneumonia.

Mol Immunol

Laboratoire UPRES EA3826 « Thérapeutiques Cliniques Et Expérimentales Des Infections », IRS2 - Nantes Biotech, Université De Nantes, Nantes, France; CHU Nantes, Pôle Anesthésie Réanimations, Service d'Anesthésie Réanimation Chirurgicale, Hôtel Dieu, Nantes, F-44093, France. Electronic address:

Published: February 2020

Background: Interleukin (IL)-22 is a cytokine involved in tissue protection and repair following lung pathologies. Interferon (IFN)-λ cytokines displayed similar properties during viral infection and a synergy of action between these two players has been documented in the intestine. We hypothesize that during Pseudomonas aeruginosa challenge, IL-22 up-regulates IFN-λ and that IFN-λ exhibits protective functions during Pseudomonas aeruginosa acute pneumonia model in mice.

Methods: Using an in vitro human alveolar epithelial cell line A549, we assessed the ability of IL-22 to enhance IFN-λ expression during infection. IFN-λ protective function was evaluated in an acute mouse pneumonia model.

Results: We first demonstrated in murine lungs that only type-II alveolar cells express IL-22 receptor and that IL-22 treatment of A549 cell line up-regulates IFN-λ expression. In a murine acute pneumonia model, IL-22 administration maintained significant IFN-λ levels in the broncho-alveolar fluids whereas IL-22 neutralization abolished IFN-λ up-regulation. In vivo administration of IFN-λ during Pseudomonas aeruginosa pneumonia improves mice outcome by dampening neutrophil recruitment and decreasing epithelium damages.

Discussion: We show here that IL-22 regulates IFN-λ levels during Pseudomonas aeruginosa pneumonia.

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Source
http://dx.doi.org/10.1016/j.molimm.2019.12.003DOI Listing

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