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Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences
BACKGROUND: Peanuts contain potent food allergens and the prevalence of allergy is reported to increase, especially in children. Since peanut sensitization may differ between different geographical regions, we wanted to investigate the sensitization pattern to the individual peanut allergens in a No...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644336/ https://www.ncbi.nlm.nih.gov/pubmed/26568764 http://dx.doi.org/10.1186/s13223-015-0095-8 |
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author | Namork, Ellen Stensby, Berit A. |
author_facet | Namork, Ellen Stensby, Berit A. |
author_sort | Namork, Ellen |
collection | PubMed |
description | BACKGROUND: Peanuts contain potent food allergens and the prevalence of allergy is reported to increase, especially in children. Since peanut sensitization may differ between different geographical regions, we wanted to investigate the sensitization pattern to the individual peanut allergens in a Norwegian population. METHODS: Cases reported to the Norwegian Food Allergy Register with sera positive to peanut extract were analyzed for specific IgE (sIgE) to the recombinant peanut allergens Ara h 1, Ara h 2, Ara h 3, Ara h 8 and Ara h 9 and to birch pollen extract. Serum samples negative to the above allergens were analyzed for sIgE to Ara h 6, and sIgE to Pru p 3 in peach were analyzed in sera positive to the cross-reactive allergen Ara h 9. RESULTS: Highest frequency of sIgE to Ara h 2, often co-sensitized to Ara h 1 and 3, were found in the small children up to 6 years of age. From the age of 6 years, sensitization to Ara h 8 was predominant. The sIgE levels to the storage proteins Ara h 1, 2 and 3 were strongly correlated, as was the sIgE levels to Ara h 8 and birch pollen extract. A low sensitization rate of sIgE to Ara h 9 in young adults was observed, which sIgE levels were very strongly correlated to Pru p 3. CONCLUSION: The sensitization to peanut allergens in a Norwegian population shows a clear age dependent pattern. The results add to the previously published research on the sensitization patterns of peanut sensitized patients in different geographical areas. |
format | Online Article Text |
id | pubmed-4644336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46443362015-11-15 Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences Namork, Ellen Stensby, Berit A. Allergy Asthma Clin Immunol Research BACKGROUND: Peanuts contain potent food allergens and the prevalence of allergy is reported to increase, especially in children. Since peanut sensitization may differ between different geographical regions, we wanted to investigate the sensitization pattern to the individual peanut allergens in a Norwegian population. METHODS: Cases reported to the Norwegian Food Allergy Register with sera positive to peanut extract were analyzed for specific IgE (sIgE) to the recombinant peanut allergens Ara h 1, Ara h 2, Ara h 3, Ara h 8 and Ara h 9 and to birch pollen extract. Serum samples negative to the above allergens were analyzed for sIgE to Ara h 6, and sIgE to Pru p 3 in peach were analyzed in sera positive to the cross-reactive allergen Ara h 9. RESULTS: Highest frequency of sIgE to Ara h 2, often co-sensitized to Ara h 1 and 3, were found in the small children up to 6 years of age. From the age of 6 years, sensitization to Ara h 8 was predominant. The sIgE levels to the storage proteins Ara h 1, 2 and 3 were strongly correlated, as was the sIgE levels to Ara h 8 and birch pollen extract. A low sensitization rate of sIgE to Ara h 9 in young adults was observed, which sIgE levels were very strongly correlated to Pru p 3. CONCLUSION: The sensitization to peanut allergens in a Norwegian population shows a clear age dependent pattern. The results add to the previously published research on the sensitization patterns of peanut sensitized patients in different geographical areas. BioMed Central 2015-11-14 /pmc/articles/PMC4644336/ /pubmed/26568764 http://dx.doi.org/10.1186/s13223-015-0095-8 Text en © Namork and Stensby. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Namork, Ellen Stensby, Berit A. Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title | Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title_full | Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title_fullStr | Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title_full_unstemmed | Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title_short | Peanut sensitization pattern in Norwegian children and adults with specific IgE to peanut show age related differences |
title_sort | peanut sensitization pattern in norwegian children and adults with specific ige to peanut show age related differences |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644336/ https://www.ncbi.nlm.nih.gov/pubmed/26568764 http://dx.doi.org/10.1186/s13223-015-0095-8 |
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