Inhibition of rBet v 1-induced basophil histamine release with specific immunotherapy -induced serum immunoglobulin G: no evidence that FcgammaRIIB signalling is important

Clin Exp Allergy. 2006 Mar;36(3):273-82. doi: 10.1111/j.1365-2222.2006.02442.x.

Abstract

Background: Human basophils and mast cells express the low-affinity immunoglobulin (Ig)G receptor FcgammaRIIB. It has previously been shown in artificial model systems that cross-linking of the high-affinity IgE receptor FcepsilonRI and FcgammaRIIB leads to inhibition of FcepsilonRI signalling.

Objective: The aim of the present study was to investigate whether cross-linking of FcepsilonRI and FcgammaRIIB contributes to IgG-mediated inhibition of histamine release in human basophils in a system using the sera from specific immunotherapy (SIT) patients and the major allergen from birch pollen, Bet v 1. As IgG4 furthermore has been proposed to have special blocking properties, we investigated the significance of IgG subclass specificity for this inhibition.

Methods: Binding of recombinant Bet v 1-IgG complexes to FcgammaRII and IgG-binding activities in the sera from 25 birch pollen-allergic patients treated with SIT were measured using (125)I-rBet v 1. Inhibition of basophil histamine release was assessed by incubating washed leucocytes with complexes of rBet v 1-IgG with or without blocking of FcgammaRII.

Results: We observed low binding of rBet v 1-IgG complexes to FcgammaRII, which was negatively correlated with the relative IgG4-binding activities. Blocking of FcgammaRII did not reverse the SIT-IgG-induced inhibition of basophil histamine release. However, IgG-binding activities correlated significantly with the ability of the SIT sera to inhibit basophil histamine release.

Conclusion: We suggest that at least in birch pollen SIT, the contribution of FcgammaRIIB-mediated inhibitory signalling to SIT-IgG-induced inhibition of human basophil histamine release is of minor importance. The main contributor to the inhibitory effect of SIT-induced IgG seems to be blocking of the allergen-IgE interaction.

MeSH terms

  • Allergens / immunology*
  • Antibody Specificity
  • Antigen-Antibody Complex / immunology
  • Antigens, Plant
  • Basophils / immunology*
  • Basophils / metabolism
  • Binding, Competitive / immunology
  • Cells, Cultured
  • Desensitization, Immunologic*
  • Histamine Release / immunology*
  • Humans
  • Immunoglobulin E / immunology
  • Immunoglobulin G / blood*
  • Receptors, IgG / immunology
  • Recombinant Proteins / immunology
  • Rhinitis, Allergic, Seasonal / immunology
  • Rhinitis, Allergic, Seasonal / therapy
  • Signal Transduction / immunology

Substances

  • Allergens
  • Antigen-Antibody Complex
  • Antigens, Plant
  • FCGR2B protein, human
  • Immunoglobulin G
  • Receptors, IgG
  • Recombinant Proteins
  • Immunoglobulin E