Carbohydrate-based particles reduce allergic inflammation in a mouse model for cat allergy

Allergy. 2008 May;63(5):518-26. doi: 10.1111/j.1398-9995.2008.01644.x.

Abstract

Background: Allergen-specific immunotherapy (ASIT) is the only treatment of allergic disease that gives long-lasting relief of symptoms. However, concerns for safety and efficiency have highlighted the need for improvement of the therapy. We have previously suggested carbohydrate-based particles (CBPs) as a novel adjuvant and allergen carrier for ASIT. Our aim of this study was to evaluate the therapeutic potential of CBPs in ASIT, employing a mouse model for cat allergy.

Methods: BALB/c mice were subcutaneously immunized with the recombinant (r) cat allergen Fel d 1 followed by intranasal challenge with cat dander extract (CDE). The sensitized mice were therapeutically treated with rFel d 1 covalently coupled to CBPs (CBP-rFel d 1). Airway hyper-reactivity (AHR), infiltration of leucocytes in bronchoalveolar lavage (BAL) fluid, allergen-specific serum immunoglobulin levels and in vitro splenocyte responses were evaluated.

Results: Mice treated with CBP-rFel d 1 showed reduced features of allergic inflammation. They responded with (i) significantly decreased AHR and infiltration of eosinophils in BAL fluid after CDE challenge, (ii) the serum level of rFel d 1-specific IgE was reduced and the level of IgG(2)a was more pronounced after CBP-rFel d 1 treatment, and (iii) there was also a tendency of decreased allergen-specific cellular response.

Conclusions: Carbohydrate-based particles are effective tools as adjuvant and allergen carriers for use in ASIT and constitutes a promising strategy to improve allergy treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / administration & dosage*
  • Animals
  • Bronchial Hyperreactivity / immunology
  • Bronchial Hyperreactivity / therapy
  • Carbohydrates / administration & dosage*
  • Carbohydrates / immunology
  • Cats
  • Desensitization, Immunologic / methods*
  • Disease Models, Animal
  • Female
  • Glycoproteins / administration & dosage*
  • Glycoproteins / adverse effects
  • Glycoproteins / genetics
  • Glycoproteins / immunology
  • Humans
  • Hypersensitivity, Immediate / etiology
  • Hypersensitivity, Immediate / immunology
  • Hypersensitivity, Immediate / therapy*
  • Inflammation / immunology
  • Inflammation / therapy*
  • Mice
  • Mice, Inbred BALB C
  • Particle Size
  • Rats
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / immunology
  • Treatment Outcome

Substances

  • Adjuvants, Immunologic
  • Carbohydrates
  • Glycoproteins
  • Recombinant Proteins
  • Fel d 1 protein, Felis domesticus