Specific allergen immunotherapy attenuates allergic airway inflammation in a rat model of Alstonia scholaris pollen induced airway allergy

Int Immunopharmacol. 2016 Jan:30:111-120. doi: 10.1016/j.intimp.2015.12.004. Epub 2015 Dec 5.

Abstract

Pollen grains are well established to be an important cause of respiratory allergy. Current pharmacologic therapies for allergic asthma do not cure the disease. Allergen specific immunotherapy is the only treatment method which re-directs the immune system away from allergic response leading to a long lasting effect. The mechanism by which immunotherapy achieves this goal is an area of active research world-wide. The present experimental study was designed to develop an experimental model of allergic lung inflammation based on a relevant human allergen, Alstonia scholaris pollen, and to establish the immunological and cellular features of specific allergen immunotherapy using this same pollen extract. Our results revealed that Alstonia scholaris pollen sensitization and challenge causes eosinophilic airway inflammation with mucin hypersecretion. This is associated with increased total IgE, increased expression of FcɛRI on lung mast cells and increased levels of IL-4, IL-5 & IL-13 as confirmed by ELISA, in-situ immunofluorescence and FACS assay. Allergen specific immunotherapy reduced airway inflammation and also decreased total IgE level, FcɛRI expression, IL-4, IL-5 & IL-13 levels. It was further noted that the reduction of these levels was more by intra-nasal route than by intra-peritoneal route. Thus we present a novel animal model of Alstonia scholaris pollen allergic disease and specific allergen immunotherapy which will pave the way towards the development of better treatment modalities.

Keywords: Airway allergy; Allergen immunotherapy; Alstonia scholaris pollen; Pollen allergy; Rat model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Allergens / immunology*
  • Alstonia / immunology
  • Animals
  • Cells, Cultured
  • Cytokines / metabolism
  • Desensitization, Immunologic*
  • Disease Models, Animal
  • Eosinophils / immunology*
  • Humans
  • Immunoglobulin E / blood
  • Mast Cells / immunology*
  • Mucinoses
  • Pneumonia / immunology
  • Pneumonia / therapy*
  • Pollen / immunology*
  • Rats
  • Rats, Wistar
  • Receptors, IgE / metabolism
  • Rhinitis, Allergic, Seasonal / immunology
  • Rhinitis, Allergic, Seasonal / therapy*
  • Th2 Cells / immunology

Substances

  • Allergens
  • Cytokines
  • FCER1A protein, rat
  • Receptors, IgE
  • Immunoglobulin E