Suppression of antigen-specific T- and B-cell responses by intranasal or oral administration of recombinant bet v 1, the major birch pollen allergen, in a murine model of type I allergy

J Allergy Clin Immunol. 1999 Jun;103(6):1202-10. doi: 10.1016/s0091-6749(99)70200-9.

Abstract

Background: Mucosal (nasal or oral) administration of soluble protein antigens induces a state of antigen-specific immunologic hyporesponsiveness. Several studies have shown that induction of mucosal tolerance can prevent the onset or reduce the severity of certain TH1 -mediated experimental autoimmune diseases. Only a few studies describe similar results for type I allergies, which are caused by excessive TH2 cell activities.

Objective: We sought to investigate whether mucosal tolerance induction would also be efficient in preventing an allergic type I immune response.

Methods: A murine model of inhalative type I allergy, leading to sensitization to birch pollen and its major allergen Bet v 1 in BALB/c mice, was used. Recombinant Bet v 1 was nasally or orally applied in low doses before sensitization. At the time of death, immediate-type skin tests were performed. Blood was taken, and serum was used for measurement of allergen-specific antibodies. Spleen cell cultures were performed to determine cytokine production (IL-4, IL-5, IL-10, and IFN-gamma), as well as levels of TGF-beta mRNA.

Results: Both nasal and oral administration of minimal doses of recombinant Bet v 1 before aerosol sensitization with birch pollen suppressed the allergen-specific antibody production of all isotypes. Consequently, the in vivo type I skin test responses to the allergen were negative in the tolerized, in contrast to the sensitized, group. Moreover, allergen-specific lymphoproliferative responses and cytokine production in vitro (ie, IFN-gamma, IL-4, IL-5, and IL-10) were markedly reduced. In contrast, expression of TGF-beta mRNA was markedly increased in spleen cells from nasally tolerized animals, indicating regulatory mechanisms for tolerance induction.

Conclusion: We conclude from the present study that nasal, as well as oral, administration of recombinant allergen is an effective way to prevent allergen-specific T- and B-cell responses in a TH2 model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Allergens*
  • Animals
  • Antibody Formation / immunology
  • Antigens, Plant
  • B-Lymphocytes / immunology*
  • Cell Division
  • Cytokines / biosynthesis
  • Disease Models, Animal
  • Epitopes
  • Female
  • Hypersensitivity, Immediate / immunology*
  • Hypersensitivity, Immediate / prevention & control
  • Hypersensitivity, Immediate / therapy
  • Immune Tolerance
  • Immunization
  • Immunoglobulin Isotypes
  • Immunosuppression Therapy
  • Immunotherapy
  • Mice
  • Mice, Inbred BALB C
  • Plant Proteins / administration & dosage*
  • Plant Proteins / immunology*
  • RNA, Messenger / analysis
  • Recombinant Proteins / immunology
  • Skin Tests
  • Spleen / cytology
  • T-Lymphocytes / immunology*
  • Th1 Cells / metabolism
  • Th2 Cells / metabolism
  • Transforming Growth Factor beta / genetics

Substances

  • Allergens
  • Antigens, Plant
  • Cytokines
  • Epitopes
  • Immunoglobulin Isotypes
  • Plant Proteins
  • RNA, Messenger
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • Bet v 1 allergen, Betula