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The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens

BACKGROUND: Allergic reactions towards the birch major pollen allergen Bet v 1 are among the most common causes of spring pollinosis in the temperate climate zone of the Northern hemisphere. Natural Bet v 1 is composed of a complex mixture of different isoforms. Detailed analysis of recombinant Bet...

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Autores principales: Wallner, Michael, Himly, Martin, Neubauer, Angela, Erler, Anja, Hauser, Michael, Asam, Claudia, Mutschlechner, Sonja, Ebner, Christof, Briza, Peter, Ferreira, Fatima
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795169/
https://www.ncbi.nlm.nih.gov/pubmed/20041109
http://dx.doi.org/10.1371/journal.pone.0008457
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author Wallner, Michael
Himly, Martin
Neubauer, Angela
Erler, Anja
Hauser, Michael
Asam, Claudia
Mutschlechner, Sonja
Ebner, Christof
Briza, Peter
Ferreira, Fatima
author_facet Wallner, Michael
Himly, Martin
Neubauer, Angela
Erler, Anja
Hauser, Michael
Asam, Claudia
Mutschlechner, Sonja
Ebner, Christof
Briza, Peter
Ferreira, Fatima
author_sort Wallner, Michael
collection PubMed
description BACKGROUND: Allergic reactions towards the birch major pollen allergen Bet v 1 are among the most common causes of spring pollinosis in the temperate climate zone of the Northern hemisphere. Natural Bet v 1 is composed of a complex mixture of different isoforms. Detailed analysis of recombinant Bet v 1 isoforms revealed striking differences in immunologic as well as allergenic properties of the molecules, leading to a classification of Bet v 1 isoforms into high, medium, and low IgE binding proteins. Especially low IgE binding Bet v 1 isoforms have been described as ideal candidates for desensitizing allergic patients with allergen specific immunotherapy (SIT). Since diagnosis and therapy of allergic diseases are highly dependent on recombinant proteins, continuous improvement of protein production is an absolute necessity. METHODOLOGY: Therefore, two different methods for recombinant production of a low IgE binding Bet v 1 isoform were applied; one based on published protocols, the other by implementing latest innovations in protein production. Both batches of Bet v 1.0401 were extensively characterized by an array of physicochemical as well as immunological methods to compare protein primary structure, purity, quantity, folding, aggregation state, thermal stability, and antibody binding capacity. CONCLUSION: The experiments demonstrated that IgE antibody binding properties of recombinant isoallergens can be significantly influenced by the production method directly affecting possible clinical applications of the molecules.
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spelling pubmed-27951692009-12-30 The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens Wallner, Michael Himly, Martin Neubauer, Angela Erler, Anja Hauser, Michael Asam, Claudia Mutschlechner, Sonja Ebner, Christof Briza, Peter Ferreira, Fatima PLoS One Research Article BACKGROUND: Allergic reactions towards the birch major pollen allergen Bet v 1 are among the most common causes of spring pollinosis in the temperate climate zone of the Northern hemisphere. Natural Bet v 1 is composed of a complex mixture of different isoforms. Detailed analysis of recombinant Bet v 1 isoforms revealed striking differences in immunologic as well as allergenic properties of the molecules, leading to a classification of Bet v 1 isoforms into high, medium, and low IgE binding proteins. Especially low IgE binding Bet v 1 isoforms have been described as ideal candidates for desensitizing allergic patients with allergen specific immunotherapy (SIT). Since diagnosis and therapy of allergic diseases are highly dependent on recombinant proteins, continuous improvement of protein production is an absolute necessity. METHODOLOGY: Therefore, two different methods for recombinant production of a low IgE binding Bet v 1 isoform were applied; one based on published protocols, the other by implementing latest innovations in protein production. Both batches of Bet v 1.0401 were extensively characterized by an array of physicochemical as well as immunological methods to compare protein primary structure, purity, quantity, folding, aggregation state, thermal stability, and antibody binding capacity. CONCLUSION: The experiments demonstrated that IgE antibody binding properties of recombinant isoallergens can be significantly influenced by the production method directly affecting possible clinical applications of the molecules. Public Library of Science 2009-12-24 /pmc/articles/PMC2795169/ /pubmed/20041109 http://dx.doi.org/10.1371/journal.pone.0008457 Text en Wallner et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wallner, Michael
Himly, Martin
Neubauer, Angela
Erler, Anja
Hauser, Michael
Asam, Claudia
Mutschlechner, Sonja
Ebner, Christof
Briza, Peter
Ferreira, Fatima
The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title_full The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title_fullStr The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title_full_unstemmed The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title_short The Influence of Recombinant Production on the Immunologic Behavior of Birch Pollen Isoallergens
title_sort influence of recombinant production on the immunologic behavior of birch pollen isoallergens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795169/
https://www.ncbi.nlm.nih.gov/pubmed/20041109
http://dx.doi.org/10.1371/journal.pone.0008457
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