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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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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. |
format | Text |
id | pubmed-2795169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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