Mouse genetic model for antigen-induced airway manifestations of asthma

• Published in: Genes and immunity Vol. 8; no. 1; pp. 28 - 34
• Main Authors: Piavaux, B, Jeurink, P V, Groot, P C, Hofman, G A, Demant, P, Van Oosterhout, A J M
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.01.2007
• Subjects: Airway management; Allergens; Allergies; Alveoli; Analysis; Animals; Antigens; Antigens - immunology; Asthma; Asthma - genetics; Asthma - immunology; Asthma - physiopathology; Bronchoalveolar Lavage Fluid - cytology; Bronchoalveolar Lavage Fluid - immunology; Bronchoconstriction; Causes of; Chromosome mapping; Disease; Disease Models, Animal; Dosage; Drug dosages; Genes; Genetic aspects; Genomes; Health aspects; Immunoglobulin E; Immunoglobulin E - blood; Immunoglobulins; Interleukin 13; Interleukin 5; Leukocytes (eosinophilic); Leukocytes (neutrophilic); Lymphocytes T; Male; Methacholine; Methacholine Chloride - immunology; Mice; Mice, Congenic; Mice, Inbred BALB C; Mice, Inbred Strains; Ovalbumin; Ovalbumin - immunology; Pathophysiology; Respiratory System - immunology; Respiratory tract; Species Specificity; United States; Netherlands
• ISSN: 1466-4879; 1476-5470
• DOI: 10.1038/sj.gene.6364354

Allergic asthma is a genetically complex disease characterized by allergen-specific immunoglobulin (Ig)E, eosinophilic inflammation of the lungs and airway hyper-responsiveness to bronchospasmogenic stimuli. In this study, we compared 13 recombinant congenic (RC) mouse strains in an ovalbumin model of allergic asthma. Different intensities and types of responses are observed throughout the RC strains. Intensities range from resistance to asthma in CcS05, to a very severe bronchoconstrictive reaction upon methacholine challenge for the parental STS strain. All strains show a 'modified' Th2 response except CcS14, which shows a 'true' Th2 response. When data from all strains are pooled, airway reactivity shows significant correlations with the serum Ig levels and the levels of interleukin (IL)-4, IL-5 and IL-13 in the broncho-alveolar lavage (BAL), at low dosage of methacholine (below 25 mg/ml), whereas at high dosage airway reactivity only correlates with BAL neutrophil levels. This indicates that at least two different mechanisms are involved in the airway reactivity to methacholine. None of these correlations can be found in every individual strain, which demonstrates that the asthma traits in this mouse model are genetically dissociated and that the loci can be genetically mapped.