House Dust Mite-Induced Allergic Airway Disease Is Independent of IgE and FcεRIα

Am J Respir Cell Mol Biol. 2017 Dec;57(6):674-682. doi: 10.1165/rcmb.2016-0356OC.

Abstract

IgE contributes to disease exacerbations but not to baseline airway hyperresponsiveness (AHR) in human asthma. In rodent allergic airway disease (AAD), mast cell and IgE dependence for the induction of AHR has only been observed when mice are immunized with a relatively weak allergen without adjuvant. To evaluate the role of IgE in murine AAD that is induced by a potent allergen, we inoculated BALB/c and FVB/N background wild-type and IgE- or FcεRIα-deficient mice intratracheally with large or limiting doses of house dust mite extract (HDM) and evaluated AHR, pulmonary eosinophilia, goblet cell metaplasia, serum IgE, and lung mastocytosis. We found that neither IgE nor FcεRIα contributed to AAD, even in mice inoculated with the lowest dose of HDM, which readily induced detectable disease, but did not increase serum IgE or pulmonary mast cell levels. In contrast, high doses of HDM strikingly increased serum IgE and pulmonary mast cells, although both AHR and airway mast cell degranulation were equally elevated in wild-type and IgE-deficient mice. Surprisingly, allergen challenge of mice with severe AAD and pulmonary mastocytosis failed to acutely increase airway resistance, lung Newtonian resistance, or hysteresis. Overall, this study shows that, although mice may not reliably model acute asthma exacerbations, mechanisms that are IgE and FcεRIα independent are responsible for AHR and airway inflammation when low doses of a potent allergen are inhaled repetitively.

Keywords: IgE; airway hyperresponsiveness; asthma; house dust mite; mast cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / immunology*
  • Animals
  • Asthma / genetics
  • Asthma / immunology*
  • Asthma / pathology
  • Goblet Cells / immunology
  • Goblet Cells / pathology
  • Humans
  • Immunoglobulin E / immunology*
  • Mastocytosis / immunology
  • Mastocytosis / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Pulmonary Eosinophilia / genetics
  • Pulmonary Eosinophilia / immunology*
  • Pyroglyphidae / immunology*
  • Receptors, IgE / genetics
  • Receptors, IgE / immunology*

Substances

  • Allergens
  • FcepsilonRIalpha protein, mouse
  • Receptors, IgE
  • Immunoglobulin E