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Peptide immunotherapy for childhood allergy - addressing translational challenges

Allergic sensitisation usually begins early in life. The number of allergens a patient is sensitised to can increase over time and the development of additional allergic conditions is increasingly recognised. Targeting allergic disease in childhood is thus likely to be the most efficacious means of...

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Autores principales: Mackenzie, Karen J, Anderton, Stephen M, Schwarze, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339362/
https://www.ncbi.nlm.nih.gov/pubmed/22409934
http://dx.doi.org/10.1186/2045-7022-1-13
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author Mackenzie, Karen J
Anderton, Stephen M
Schwarze, Jürgen
author_facet Mackenzie, Karen J
Anderton, Stephen M
Schwarze, Jürgen
author_sort Mackenzie, Karen J
collection PubMed
description Allergic sensitisation usually begins early in life. The number of allergens a patient is sensitised to can increase over time and the development of additional allergic conditions is increasingly recognised. Targeting allergic disease in childhood is thus likely to be the most efficacious means of reducing the overall burden of allergic disease. Specific immunotherapy involves administering protein allergen to tolerise allergen reactive CD4(+ )T cells, thought key in driving allergic responses. Yet specific immunotherapy risks allergic reactions including anaphylaxis as a consequence of preformed allergen-specific IgE antibodies binding to the protein, subsequent cross-linking and mast cell degranulation. CD4(+ )T cells direct their responses to short "immunodominant" peptides within the allergen. Such peptides can be given therapeutically to induce T cell tolerance without facilitating IgE cross-linking. Peptide immunotherapy (PIT) offers attractive treatment potential for allergic disease. However, PIT has not yet been shown to be effective in children. This review discusses the immunological mechanisms implicated in PIT and briefly covers outcomes from adult PIT trials. This provides a context for discussion of the challenges for the application of PIT, both generally and more specifically in relation to children.
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spelling pubmed-33393622012-05-01 Peptide immunotherapy for childhood allergy - addressing translational challenges Mackenzie, Karen J Anderton, Stephen M Schwarze, Jürgen Clin Transl Allergy Review Allergic sensitisation usually begins early in life. The number of allergens a patient is sensitised to can increase over time and the development of additional allergic conditions is increasingly recognised. Targeting allergic disease in childhood is thus likely to be the most efficacious means of reducing the overall burden of allergic disease. Specific immunotherapy involves administering protein allergen to tolerise allergen reactive CD4(+ )T cells, thought key in driving allergic responses. Yet specific immunotherapy risks allergic reactions including anaphylaxis as a consequence of preformed allergen-specific IgE antibodies binding to the protein, subsequent cross-linking and mast cell degranulation. CD4(+ )T cells direct their responses to short "immunodominant" peptides within the allergen. Such peptides can be given therapeutically to induce T cell tolerance without facilitating IgE cross-linking. Peptide immunotherapy (PIT) offers attractive treatment potential for allergic disease. However, PIT has not yet been shown to be effective in children. This review discusses the immunological mechanisms implicated in PIT and briefly covers outcomes from adult PIT trials. This provides a context for discussion of the challenges for the application of PIT, both generally and more specifically in relation to children. BioMed Central 2011-11-07 /pmc/articles/PMC3339362/ /pubmed/22409934 http://dx.doi.org/10.1186/2045-7022-1-13 Text en Copyright ©2011 Mackenzie et al; 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 Review
Mackenzie, Karen J
Anderton, Stephen M
Schwarze, Jürgen
Peptide immunotherapy for childhood allergy - addressing translational challenges
title Peptide immunotherapy for childhood allergy - addressing translational challenges
title_full Peptide immunotherapy for childhood allergy - addressing translational challenges
title_fullStr Peptide immunotherapy for childhood allergy - addressing translational challenges
title_full_unstemmed Peptide immunotherapy for childhood allergy - addressing translational challenges
title_short Peptide immunotherapy for childhood allergy - addressing translational challenges
title_sort peptide immunotherapy for childhood allergy - addressing translational challenges
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339362/
https://www.ncbi.nlm.nih.gov/pubmed/22409934
http://dx.doi.org/10.1186/2045-7022-1-13
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