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Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease

INTRODUCTION: Allergic reactions are mediated by human IgE antibodies that bind to and cross-link allergen molecules. The sites on allergens that are recognized by IgE antibodies have been difficult to investigate because of the paucity of IgE antibodies in a human serum. Here, we report the product...

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Autores principales: Smith, Bryan R. E., Reid Black, Kristina, Bermingham, Max, Agah, Sayeh, Glesner, Jill, Versteeg, Serge A., van Ree, Ronald, Pena-Amelunxen, Glorismer, Aglas, Lorenz, Smith, Scott A., Pomés, Anna, Chapman, Martin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602672/
https://www.ncbi.nlm.nih.gov/pubmed/37901762
http://dx.doi.org/10.3389/falgy.2023.1270326
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author Smith, Bryan R. E.
Reid Black, Kristina
Bermingham, Max
Agah, Sayeh
Glesner, Jill
Versteeg, Serge A.
van Ree, Ronald
Pena-Amelunxen, Glorismer
Aglas, Lorenz
Smith, Scott A.
Pomés, Anna
Chapman, Martin D.
author_facet Smith, Bryan R. E.
Reid Black, Kristina
Bermingham, Max
Agah, Sayeh
Glesner, Jill
Versteeg, Serge A.
van Ree, Ronald
Pena-Amelunxen, Glorismer
Aglas, Lorenz
Smith, Scott A.
Pomés, Anna
Chapman, Martin D.
author_sort Smith, Bryan R. E.
collection PubMed
description INTRODUCTION: Allergic reactions are mediated by human IgE antibodies that bind to and cross-link allergen molecules. The sites on allergens that are recognized by IgE antibodies have been difficult to investigate because of the paucity of IgE antibodies in a human serum. Here, we report the production of unique human IgE monoclonal antibodies to major inhaled allergens and food allergens that can be produced at scale in perpetuity. MATERIALS AND METHODS: The IgE antibodies were derived from peripheral blood mononuclear cells of symptomatic allergic patients, mostly children aged 3–18 years, using hybridoma fusion technology. Total IgE and allergen-specific IgE was measured by ImmunoCAP. Their specificity was confirmed through ELISA and immunoblotting. Allergenic potency measurements were determined by ImmunoCAP inhibition. Biological activity was determined in vitro by comparing β-hexosaminidase release from a humanized rat basophilic cell line. RESULTS: Human IgE monoclonal antibodies (n = 33) were derived from 17 allergic patients with symptoms of allergic rhinitis, asthma, atopic dermatitis, food allergy, eosinophilic esophagitis, or red meat allergy. The antibodies were specific for five inhaled allergens, nine food allergens, and alpha-gal and had high levels of IgE (53,450–1,702,500 kU/L) with ratios of specific IgE to total IgE ranging from <0.01 to 1.39. Sigmoidal allergen binding curves were obtained through ELISA, with low limits of detection (<1 kU/L). Allergen specificity was confirmed through immunoblotting. Pairs of IgE monoclonal antibodies to Ara h 6 were identified that cross-linked after allergen stimulation and induced release of significant levels of β-hexosaminidase (35%–80%) from a humanized rat basophilic cell line. CONCLUSIONS: Human IgE monoclonal antibodies are unique antibody molecules with potential applications in allergy diagnosis, allergen standardization, and identification of allergenic epitopes for the development of allergy therapeutics. The IgE antibody probes will enable the unequivocal localization and validation of allergenic epitopes.
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spelling pubmed-106026722023-10-27 Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease Smith, Bryan R. E. Reid Black, Kristina Bermingham, Max Agah, Sayeh Glesner, Jill Versteeg, Serge A. van Ree, Ronald Pena-Amelunxen, Glorismer Aglas, Lorenz Smith, Scott A. Pomés, Anna Chapman, Martin D. Front Allergy Allergy INTRODUCTION: Allergic reactions are mediated by human IgE antibodies that bind to and cross-link allergen molecules. The sites on allergens that are recognized by IgE antibodies have been difficult to investigate because of the paucity of IgE antibodies in a human serum. Here, we report the production of unique human IgE monoclonal antibodies to major inhaled allergens and food allergens that can be produced at scale in perpetuity. MATERIALS AND METHODS: The IgE antibodies were derived from peripheral blood mononuclear cells of symptomatic allergic patients, mostly children aged 3–18 years, using hybridoma fusion technology. Total IgE and allergen-specific IgE was measured by ImmunoCAP. Their specificity was confirmed through ELISA and immunoblotting. Allergenic potency measurements were determined by ImmunoCAP inhibition. Biological activity was determined in vitro by comparing β-hexosaminidase release from a humanized rat basophilic cell line. RESULTS: Human IgE monoclonal antibodies (n = 33) were derived from 17 allergic patients with symptoms of allergic rhinitis, asthma, atopic dermatitis, food allergy, eosinophilic esophagitis, or red meat allergy. The antibodies were specific for five inhaled allergens, nine food allergens, and alpha-gal and had high levels of IgE (53,450–1,702,500 kU/L) with ratios of specific IgE to total IgE ranging from <0.01 to 1.39. Sigmoidal allergen binding curves were obtained through ELISA, with low limits of detection (<1 kU/L). Allergen specificity was confirmed through immunoblotting. Pairs of IgE monoclonal antibodies to Ara h 6 were identified that cross-linked after allergen stimulation and induced release of significant levels of β-hexosaminidase (35%–80%) from a humanized rat basophilic cell line. CONCLUSIONS: Human IgE monoclonal antibodies are unique antibody molecules with potential applications in allergy diagnosis, allergen standardization, and identification of allergenic epitopes for the development of allergy therapeutics. The IgE antibody probes will enable the unequivocal localization and validation of allergenic epitopes. Frontiers Media S.A. 2023-10-12 /pmc/articles/PMC10602672/ /pubmed/37901762 http://dx.doi.org/10.3389/falgy.2023.1270326 Text en © 2023 Smith, Reid Black, Bermingham, Agah, Glesner, Versteeg, van Ree, Pena-Amelunxen, Aglas, Smith, Pomés and Chapman. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Allergy
Smith, Bryan R. E.
Reid Black, Kristina
Bermingham, Max
Agah, Sayeh
Glesner, Jill
Versteeg, Serge A.
van Ree, Ronald
Pena-Amelunxen, Glorismer
Aglas, Lorenz
Smith, Scott A.
Pomés, Anna
Chapman, Martin D.
Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title_full Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title_fullStr Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title_full_unstemmed Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title_short Unique allergen-specific human IgE monoclonal antibodies derived from patients with allergic disease
title_sort unique allergen-specific human ige monoclonal antibodies derived from patients with allergic disease
topic Allergy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602672/
https://www.ncbi.nlm.nih.gov/pubmed/37901762
http://dx.doi.org/10.3389/falgy.2023.1270326
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