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Assessment of allergen cross-reactivity

The prediction of allergen cross-reactivity is currently largely based on linear sequence data, but will soon include 3D information on homology among surface exposed residues. To evaluate procedures for these predictions, we need ways to quantitatively assess actual cross-reactivity between two all...

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Autor principal: Aalberse, Rob C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797810/
https://www.ncbi.nlm.nih.gov/pubmed/17291349
http://dx.doi.org/10.1186/1476-7961-5-2
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author Aalberse, Rob C
author_facet Aalberse, Rob C
author_sort Aalberse, Rob C
collection PubMed
description The prediction of allergen cross-reactivity is currently largely based on linear sequence data, but will soon include 3D information on homology among surface exposed residues. To evaluate procedures for these predictions, we need ways to quantitatively assess actual cross-reactivity between two allergens. Three parameters are mentioned: 1) the fraction of the epitopes that is cross-reactive; 2) the fraction of IgE that is cross-reactive; 3) the relative affinity of the interaction between IgE and the two allergens. This editorial briefly compares direct binding protocols with the often more appropriate reciprocal inhibition protocols. The latter type of protocol provides information on symmetric versus asymmetric cross-reactivity, and thus on the distinction between complete (= sensitising) allergens versus incomplete, cross-reacting allergens. The need to define the affinity threshold of the assay and a caveat on the use of serum pools are also discussed.
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spelling pubmed-17978102007-02-15 Assessment of allergen cross-reactivity Aalberse, Rob C Clin Mol Allergy Commentary The prediction of allergen cross-reactivity is currently largely based on linear sequence data, but will soon include 3D information on homology among surface exposed residues. To evaluate procedures for these predictions, we need ways to quantitatively assess actual cross-reactivity between two allergens. Three parameters are mentioned: 1) the fraction of the epitopes that is cross-reactive; 2) the fraction of IgE that is cross-reactive; 3) the relative affinity of the interaction between IgE and the two allergens. This editorial briefly compares direct binding protocols with the often more appropriate reciprocal inhibition protocols. The latter type of protocol provides information on symmetric versus asymmetric cross-reactivity, and thus on the distinction between complete (= sensitising) allergens versus incomplete, cross-reacting allergens. The need to define the affinity threshold of the assay and a caveat on the use of serum pools are also discussed. BioMed Central 2007-02-09 /pmc/articles/PMC1797810/ /pubmed/17291349 http://dx.doi.org/10.1186/1476-7961-5-2 Text en Copyright © 2007 Aalberse; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Aalberse, Rob C
Assessment of allergen cross-reactivity
title Assessment of allergen cross-reactivity
title_full Assessment of allergen cross-reactivity
title_fullStr Assessment of allergen cross-reactivity
title_full_unstemmed Assessment of allergen cross-reactivity
title_short Assessment of allergen cross-reactivity
title_sort assessment of allergen cross-reactivity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797810/
https://www.ncbi.nlm.nih.gov/pubmed/17291349
http://dx.doi.org/10.1186/1476-7961-5-2
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