Impaired mucus clearance exacerbates allergen-induced type 2 airway inflammation in juvenile mice

J Allergy Clin Immunol. 2017 Jul;140(1):190-203.e5. doi: 10.1016/j.jaci.2016.09.045. Epub 2016 Nov 16.

Abstract

Background: Type 2 airway inflammation plays a central role in the pathogenesis of allergen-induced asthma, but the underlying mechanisms remain poorly understood. Recently, we demonstrated that reduced mucociliary clearance, a characteristic feature of asthma, produces spontaneous type 2 airway inflammation in juvenile β-epithelial Na+ channel (Scnn1b)-transgenic (Tg) mice.

Objective: We sought to determine the role of impaired mucus clearance in the pathogenesis of allergen-induced type 2 airway inflammation and identify cellular sources of the signature cytokine IL-13.

Methods: We challenged juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and house dust mite allergen and compared the effects on airway eosinophilia, type 2 cytokine levels, goblet cell metaplasia, and airway hyperresponsiveness. Furthermore, we determined cellular sources of IL-13 and effects of genetic deletion of the key type 2 signal-transducing molecule signal transducer and activator of transcription 6 (STAT6) and evaluated the effects of therapeutic improvement of mucus clearance.

Results: Reduced mucociliary allergen clearance exacerbated Stat6-dependent secretion of type 2 cytokines, airway eosinophilia, and airway hyperresponsiveness in juvenile Scnn1b-Tg mice. IL-13 levels were increased in airway epithelial cells, macrophages, type 2 innate lymphoid cells, and TH2 cells along with increased Il33 expression in the airway epithelium of Scnn1b-Tg mice. Treatment with the epithelial Na+ channel blocker amiloride, improving airway surface hydration and mucus clearance, reduced allergen-induced inflammation in Scnn1b-Tg mice.

Conclusion: Our data support that impaired clearance of inhaled allergens triggering IL-13 production by multiple cell types in the airways plays an important role in the pathogenesis of type 2 airway inflammation and suggests therapeutic improvement of mucociliary clearance as a novel treatment strategy for children with allergen-induced asthma.

Keywords: IL-13; IL-33; Type 2 inflammation; airway epithelium; mucociliary clearance.

MeSH terms

  • Allergens / immunology
  • Amiloride / pharmacology
  • Amiloride / therapeutic use
  • Animals
  • Aspergillus fumigatus / immunology
  • Asthma / drug therapy
  • Asthma / immunology*
  • Asthma / physiopathology*
  • Bronchoalveolar Lavage Fluid / cytology
  • Cell Count
  • Cells, Cultured
  • Disease Models, Animal
  • Epithelial Cells / drug effects
  • Epithelial Cells / immunology
  • Epithelial Sodium Channels / genetics
  • Interleukin-13 / immunology*
  • Lung / cytology
  • Lung / immunology
  • Mice, Transgenic
  • Mucociliary Clearance*
  • Pyroglyphidae / immunology
  • STAT6 Transcription Factor / genetics
  • Sodium Channel Blockers / pharmacology
  • Sodium Channel Blockers / therapeutic use

Substances

  • Allergens
  • Epithelial Sodium Channels
  • Interleukin-13
  • STAT6 Transcription Factor
  • Scnn1b protein, mouse
  • Sodium Channel Blockers
  • Stat6 protein, mouse
  • Amiloride