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J Allergy Clin Immunol ; 111(6): 1262-8, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12789227

ABSTRACT

BACKGROUND: IgE antibodies are key players in immediate hypersensitivity reactions. Allergen characterization and standardization is usually based on the sera of allergic patients, whereas monoclonal IgE antibodies specific for clinically relevant allergens are very rare. OBJECTIVE: The aim of this study was to establish IgE mAbs specific for birch pollen allergens, because these are important inhalant allergens. METHODS: IgE-producing hybridomas were identified by using the highly sensitive rat basophilic leukemia cell mediator release assay with enhanced allergen stimulation by additional cross-linking with birch pollen-specific IgG antibodies. The obtained IgE mAbs were characterized by immunologic methods and by cDNA sequencing. RESULTS: Seven IgE mAbs specific for the birch pollen allergens Bet v 1 or Bet v 6 were obtained and were all biologically active in mast cell-based assays. Mediator release experiments with mAb combinations indicated that 2 different epitope regions were recognized on Bet v 1, whereas the 2 Bet v 6-specific mAbs bound to the same epitope region. After sensitization of rat basophilic leukemia cells with IgE mAbs, different amounts of Bet v 1 or Bet v 6 were detected in commercial diagnostic allergen reagents, whereas sensitization with polyclonal IgE resulted in similar allergenic potency of all products. CONCLUSIONS: IgE mAbs represent promising novel tools for allergen characterization and component-resolved standardization of allergen extracts.


Subject(s)
Allergens/immunology , Antibodies, Monoclonal/immunology , Betula/immunology , Immunoglobulin E/immunology , Pollen/immunology , Allergens/chemistry , Animals , Antibodies, Monoclonal/chemistry , Antibody Specificity , Antigens, Plant , Basophils/immunology , Cell Degranulation , Cell Extracts/standards , Epitopes/immunology , Hybridomas , Immunoglobulin E/chemistry , Immunoglobulin Heavy Chains/analysis , Immunoglobulin Light Chains/analysis , Mice , Mice, Inbred BALB C , Plant Proteins/chemistry , Plant Proteins/immunology , Rats , Tumor Cells, Cultured
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