Abrogation of lung inflammation in sensitized Stat6-deficient mice is dependent on the allergen inhalation procedure

Br J Pharmacol. 2000 Aug;130(7):1581-8. doi: 10.1038/sj.bjp.0703501.

Abstract

Conflicting results have been reported about the role of Stat6 in allergen-induced airway inflammation. We have studied the influence of the allergen inhalation procedure on the inflammatory response using wild-type and Stat6-deficient mice generated on a C57BL/6 background. Animals were immunized i.p. on day 0 and 7 with ovalbumin (OVA) and then received aerosolized OVA or phosphate buffer saline challenge (acute on day 14; chronic on day 14, 15, 16, 17 and 18) before being sacrificed at different time points. Following an acute challenge, Stat6-deficiency fully abrogated the increase in serum IgE levels and the development of lung inflammation (inflammatory cell infiltration, IL-4 and IL-5 release, and increase in plasma leakage). Following chronic challenge, despite the absence of IgE, IL-4 and IL-5, Stat6-deficient mice develop a characteristic lung inflammation, although the intensity was smaller when compared with the wild-type mice. OVA-induced early bronchoconstriction was observed in wild-type mice only after chronic challenge, and this was totally abrogated in the Stat6-deficient animals. These results suggest that Stat6 signalling is essential for the development of allergic airway inflammation following an acute allergen exposure. However, in a more chronic situation, the airway inflammatory response seems to be only partially mediated by Stat6.

MeSH terms

  • Allergens / immunology*
  • Allergens / pharmacology
  • Analysis of Variance
  • Animals
  • Bronchoalveolar Lavage
  • Bronchoconstriction / drug effects
  • Cytokines / metabolism
  • Eosinophil Peroxidase
  • Female
  • Fibronectins / metabolism
  • Immunoglobulin E / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Peroxidases / metabolism
  • Pneumonia / immunology*
  • Pneumonia / metabolism
  • Pneumonia / physiopathology
  • STAT6 Transcription Factor
  • Trans-Activators / deficiency
  • Trans-Activators / immunology*

Substances

  • Allergens
  • Cytokines
  • Fibronectins
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • Immunoglobulin E
  • Eosinophil Peroxidase
  • Peroxidases