The annexin A1/FPR2 signaling axis expands alveolar macrophages, limits viral replication, and attenuates pathogenesis in the murine influenza A virus infection model. Issue 11 (2nd October 2019)

• Record Type: Journal Article
• Authors: Schloer, Sebastian; Hübel, Nicole; Masemann, Dörthe; Pajonczyk, Denise; Brunotte, Linda; Ehrhardt, Christina; Brandenburg, Lars‐Ove; Ludwig, Stephan; Gerke, Volker; Rescher, Ursula
• Is Part Of: FASEB journal. Volume 33:Issue 11(2019)
• Page Start: 12188
• Page End: 12199
• Publication Date: 2019-10-02
• Subjects: pattern recognition receptors -- innate immune system -- mucosal immunity; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201901265R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Pattern recognition receptors (PRRs) are key elements in the innate immune response. Formyl peptide receptor (FPR) 2 is a PRR that, in addition to proinflammatory, pathogen‐derived compounds, also recognizes the anti‐inflammatory endogenous ligand annexin A1 (AnxA1). Because the contribution of this signaling axis in viral infections is undefined, we investigated AnxA1‐mediated FPR2 activation on influenza A virus (IAV) infection in the murine model. AnxA1‐treated mice displayed significantly attenuated pathology upon a subsequent IAV infection with significantly improved survival, impaired viral replication in the respiratory tract, and less severe lung damage. The AnxA1‐mediated protection against IAV infection was not caused by priming of the type I IFN response but was associated with an increase in the number of alveolar macrophages (AMs) and enhanced pulmonary expression of the AM‐regulating cytokine granulocyte‐M‐CSF (GM‐CSF). Both AnxA1‐mediated increase in AM levels and GM‐CSF production were abrogated when mouse (m)FPR2 signaling was antagonized but remained up‐regulated in mice genetically deleted for mFPR1, an mFPR2 isoform also serving as AnxA1 receptor. Our results indicate a novel protective function of the AnxA1‐FPR2 signaling axis in IAV pathology via GM‐CSF‐associated maintenance of AMs, expanding knowledge on the potential use of proresolving mediators in host defense against pathogens.—Schloer, S., Hübel, N., Masemann, D., Pajonczyk, D., Brunotte, L., Ehrhardt, C., Brandenburg, L.‐O., Ludwig, S., Gerke, V., Rescher, U. The annexin A1/FPR2 signaling axis expands alveolar macrophages, limits viral replication, and attenuates pathogenesis in the murine influenza A virus infection model. FASEB J. 33, 12188–12199 (2019). www.fasebj.org