Gender difference in allergic airway remodelling and immunoglobulin production in mouse model of asthma

Respirology. 2013 Jul;18(5):797-806. doi: 10.1111/resp.12078.


Background and objective: Epidemiological studies have shown that the prevalence of adult asthma and severe asthma is higher in women. It has also been reported that female mice are more susceptible than males to the development of allergic airway inflammation and airway hyperresponsiveness (AHR). The influence of gender difference in the pathogenesis of severe asthma, especially airway remodelling in an animal model, has been studied rarely. We investigated gender difference in the development of airway remodelling using a long-term antigen-challenged mouse asthma model.

Methods: Following ovalbumin (OVA)/alum intraperitoneal injection, male or female mice (BALB/c) were challenged with aerosolized 1% OVA on 3 days/week for 5 weeks, and differences in AHR, airway inflammation and airway remodelling between the sexes were investigated.

Results: In OVA-sensitized and OVA-challenged (OVA/OVA) female mice, eosinophils, lymphocytes, T-helper type 2 cytokines and growth factors in bronchoalveolar lavage fluid were increased compared with OVA/OVA male mice. Histological features of airway remodelling were also increased in OVA/OVA female mice. Serum total and OVA-specific immunoglobulin E (IgE) and serum IgA were significantly elevated in OVA/OVA female mice.

Conclusions: These results indicate that female mice experience more airway remodelling compared with male mice. These results suggest the involvement of sex hormones and gender differences in cellular functions in airway remodelling.

Publication types

  • Comparative Study

MeSH terms

  • Airway Remodeling / physiology*
  • Animals
  • Asthma / chemically induced
  • Asthma / metabolism*
  • Asthma / physiopathology*
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Gonadal Steroid Hormones / physiology
  • Immunoglobulin A / metabolism*
  • Immunoglobulin E / metabolism*
  • Immunoglobulin G / metabolism*
  • Injections, Intraperitoneal
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin / administration & dosage
  • Ovalbumin / adverse effects
  • Sex Factors*


  • Chemokines
  • Cytokines
  • Gonadal Steroid Hormones
  • Immunoglobulin A
  • Immunoglobulin G
  • Intercellular Signaling Peptides and Proteins
  • Immunoglobulin E
  • Ovalbumin