TLR2-mediated innate immune priming boosts lung anti-viral immunity. Issue 1 (1st July 2021)

• Record Type: Journal Article
• Authors: Girkin, Jason; Loo, Su-Ling; Esneau, Camille; Maltby, Steven; Mercuri, Francesca; Chua, Brendon; Reid, Andrew T.; Veerati, Punnam Chander; Grainge, Chris L.; Wark, Peter A.B.; Knight, Darryl; Jackson, David; Demaison, Christophe; Bartlett, Nathan W.
• Is Part Of: European respiratory journal. Volume 58:Issue 1(2021)
• Publication Date: 2021-07-01
• Subjects: Respiratory organs -- Diseases -- Periodicals; Respiration -- Periodicals; 616.2
• DOI: 10.1183/13993003.01584-2020
• Languages: English
• ISSNs: 0903-1936

Abstract

Background: We assessed whether Toll-like receptor (TLR)2 activation boosts the innate immune response to rhinovirus infection, as a treatment strategy for virus-induced respiratory diseases. Methods: We employed treatment with a novel TLR2 agonist (INNA-X) prior to rhinovirus infection in mice, and INNA-X treatment in differentiated human bronchial epithelial cells derived from asthmatic-donors. We assessed viral load, immune cell recruitment, cytokines, type I and III interferon (IFN) production, as well as the lung tissue and epithelial cell immune transcriptome. Results: We show, in vivo, that a single INNA-X treatment induced innate immune priming characterised by low-level IFN-λ, Fas ligand, chemokine expression and airway lymphocyte recruitment. Treatment 7 days before infection significantly reduced lung viral load, increased IFN-β/λ expression and inhibited neutrophilic inflammation. Corticosteroid treatment enhanced the anti-inflammatory effects of INNA-X. Treatment 1 day before infection increased expression of 190 lung tissue immune genes. This tissue gene expression signature was absent with INNA-X treatment 7 days before infection, suggesting an alternate mechanism, potentially via establishment of immune cell-mediated mucosal innate immunity. In vitro, INNA-X treatment induced a priming response defined by upregulated IFN-λ, chemokine and anti-microbial gene expression that preceded an accelerated response to infection enriched for nuclear factor (NF)-κB-regulated genes and reduced viral loads, even in epithelial cells derived from asthmatic donors with intrinsic delayed anti-viral immune response. Conclusion: Airway epithelial cell TLR2 activation induces prolonged innate immune priming, defined by early NF-κB activation, IFN-λ expression and lymphocyte recruitment. This response enhanced anti-viral innate immunity and reduced virus-induced airway inflammation. TLR2-agonist treatment to the respiratory tract activates airway epithelial cells to prime the innate immune system to rapidly respond to infection and reduce virus-induced inflammation, including in the context of corticosteroid treatment and in asthma https://bit.ly/3g02Q4M