Isoforms of atopic allergens with reduced allergenicity but conserved T cell antigenicity: possible use for specific immunotherapy

Int Arch Allergy Immunol. 1997 May-Jul;113(1-3):125-7. doi: 10.1159/000237524.

Abstract

Background: We analyzed the T cell activation potency and the IgE-binding properties (allergenicity) of nine isoforms of Bet v 1, the major allergen of birch pollen.

Methods: The capacity of recombinant Bet v 1 isoforms to bind serum IgE from allergic patients was evaluated by immunoblot experiments and skin prick tests. The potency of Bet v 1 isoallergens to activate T lymphocytes from birch-pollen-allergic patients was assayed using allergen-specific T cell clones.

Results: According to their ability to bind IgE from allergic patients in immunoblot experiments, Bet v 1 isoforms can be grouped into high-IgE-binding molecules and molecules with low/no IgE-binding activity. Representatively, isoform d was used in skin tests. Skin prick tests revealed no potency of this isoform to induce wheal and flare reactions in the skin of birch-pollen-allergic individuals. In contrast, isoform a and natural Bet v 1 displayed high allergenicity in vivo. On the other hand, Bet v 1 isoform d (low allergenicity) displayed significant higher T cell activation potency when compared to isoform a (high allergenicity).

Conclusion: Based on these findings, we propose a new form of specific immunotherapy using hypoallergenic recombinant allergen isoforms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / immunology*
  • Antigens, Plant
  • Humans
  • Immunoglobulin E / immunology
  • Immunotherapy
  • Lymphocyte Activation
  • Plant Proteins / immunology*
  • T-Lymphocytes / immunology*

Substances

  • Allergens
  • Antigens, Plant
  • Plant Proteins
  • Bet v 1 allergen, Betula
  • Immunoglobulin E