Eosinophilic rhinitis accompanies the development of lower airway inflammation and hyper-reactivity in sensitized mice exposed to aerosolized allergen

Clin Exp Allergy. 2001 May;31(5):782-90. doi: 10.1046/j.1365-2222.2001.01081.x.

Abstract

Background: Allergic rhinitis is a risk factor for the development of asthma. About 80% of asthmatic patients also have rhinitis. However, the pattern of induction of allergic rhinitis and asthma remains unclear.

Objective: The purpose of this study was to investigate the development of upper airway inflammation in mice during the development of an asthma-like disease and after an acute allergen provocation.

Methods: BALB-c mice were sensitized intraperitoneally (i.p) to ovalbumin (OA, days 1-13) and were challenged with aerosols of either OA or saline on 8 consecutive days (days 33-40). In a second experiment, chronic exposure for 8 days was followed by 10 days of rest and then an acute nebulized allergen provocation was performed (day 50). Inflammatory parameters were investigated at different time-points.

Results: Upper and lower eosinophilic airway inflammation were simultaneously induced in the course of repeated inhalations of nebulized OA, as shown by analyses of nasal and broncho-alveolar lavage fluids and histological sections of the nose and bronchi. Mice that developed bronchial hyper-responsiveness also had increased thickness of the nasal mucosa on magnetic resonance image (MRI) scans. When chronic exposure was followed by acute allergen provocation, the latter caused a systemic increase in IL-5 levels, with a concomitant rise in blood and airway eosinophils, primarily in the nose.

Conclusions: Simultaneous induction of eosinophilic inflammation in the nose and lungs was found in a mouse model of respiratory allergy. These findings support the viewpoint that upper and lower airway disease represent a continuum of inflammation involving one common airway and provide evidence for the concept of global airway inflammation after inhalation of allergen.

Publication types

  • Comparative Study

MeSH terms

  • Aerosols
  • Allergens / administration & dosage
  • Allergens / immunology*
  • Animals
  • Antibody Specificity / drug effects
  • Antibody Specificity / immunology
  • Bronchial Hyperreactivity / complications*
  • Bronchial Provocation Tests
  • Bronchoalveolar Lavage Fluid / cytology
  • Disease Models, Animal
  • Eosinophilia / complications*
  • Eosinophils / drug effects
  • Follow-Up Studies
  • Immunization*
  • Immunoglobulin E / blood
  • Immunoglobulin E / drug effects
  • Immunoglobulin E / immunology
  • Inhalation Exposure
  • Interleukin-5 / blood
  • Leukocyte Count
  • Lymphocyte Count
  • Magnetic Resonance Imaging
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Nasal Lavage Fluid / cytology
  • Nasal Mucosa / diagnostic imaging
  • Ovalbumin / administration & dosage
  • Ovalbumin / immunology
  • Pilot Projects
  • Pneumonia / chemically induced*
  • Pneumonia / complications
  • Radiography
  • Rhinitis / complications*

Substances

  • Aerosols
  • Allergens
  • Interleukin-5
  • Immunoglobulin E
  • Ovalbumin