The blocking activity of birch pollen-specific immunotherapy-induced IgG4 is not qualitatively superior to that of other IgG subclasses

• Published in: Molecular immunology Vol. 41; no. 5; pp. 471 - 478
• Main Authors: Ejrnaes, Anne M, Bodtger, Uffe, Larsen, Jørgen N, Svenson, Morten
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.07.2004
• Subjects: Allergens - immunology; Allergens - therapeutic use; Allergy; Antibodies - blood; Antibodies - immunology; Antibody Specificity; Antigen-Antibody Reactions; Antigens, Plant; Betula - immunology; Betula verrucosa; Binding, Competitive; Blocking antibodies; Cross Reactions - immunology; Humans; Hypersensitivity - therapy; IgE; Immunoglobulin E - blood; Immunoglobulin E - immunology; Immunoglobulin G - blood; Immunoglobulin G - classification; Immunoglobulin G - immunology; Immunotherapy; Pollen - immunology; Recombinant Proteins; Allergy; Immunotherapy; IgE; Blocking antibodies
• ISSN: 0161-5890; 1872-9142
• DOI: 10.1016/j.molimm.2004.04.018

Allergen-specific IgG antibodies induced by specific immunotherapy (SIT) interfere with the allergen–IgE interaction, and act as blocking antibodies in vitro. It has been hypothesised that IgG4, as opposed to other IgG subclasses, is particularly important in this function, which may play a role for the clinical efficacy of SIT. In this study, fractionated serum samples from 14 SIT-treated birch pollen allergic individuals enabled determination of the inhibitory capacity of IgG4 alone versus non-IgG4 IgG. Allergen-binding activities of IgG and the IgG-mediated inhibition of allergen binding to autologous IgE were detected using 125I-labelled rBet v 1.2801, a recombinant variant of the major allergen of Betula verrucosa pollen. Results show that IgG4-depletion resulted in equivalent reductions in binding and blocking activities. In contrast, a significant but less than two-fold higher relative blocking activity was found in the purified IgG4 fraction. There was no significant difference in the binding avidities (1/ K d) measured in the two IgG fractions. Thus, it appears that SIT-induced specific IgG4 contributes to the IgG blocking of allergen binding to IgE in a simple quantitative manner and not by a particular intrinsic blocking activity.