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Immunotherapy with Allergen Peptides

Specific allergen immunotherapy (SIT) is disease-modifying and efficacious. However, the use of whole allergen preparations is associated with frequent allergic adverse events during treatment. Many novel approaches are being designed to reduce the allergenicity of immunotherapy preparations whilst...

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Detalles Bibliográficos
Autor principal: Larché, Mark
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873623/
https://www.ncbi.nlm.nih.gov/pubmed/20525144
http://dx.doi.org/10.1186/1710-1492-3-2-53
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author Larché, Mark
author_facet Larché, Mark
author_sort Larché, Mark
collection PubMed
description Specific allergen immunotherapy (SIT) is disease-modifying and efficacious. However, the use of whole allergen preparations is associated with frequent allergic adverse events during treatment. Many novel approaches are being designed to reduce the allergenicity of immunotherapy preparations whilst maintaining immunogenicity. One approach is the use of short synthetic peptides which representing dominant T cell epitopes of the allergen. Short peptides exhibit markedly reduced capacity to cross link IgE and activate mast cells and basophils, due to lack of tertiary structure. Murine pre-clinical studies have established the feasibility of this approach and clinical studies are currently in progress in both allergic and autoimmune diseases.
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spelling pubmed-28736232010-05-20 Immunotherapy with Allergen Peptides Larché, Mark Allergy Asthma Clin Immunol Research Specific allergen immunotherapy (SIT) is disease-modifying and efficacious. However, the use of whole allergen preparations is associated with frequent allergic adverse events during treatment. Many novel approaches are being designed to reduce the allergenicity of immunotherapy preparations whilst maintaining immunogenicity. One approach is the use of short synthetic peptides which representing dominant T cell epitopes of the allergen. Short peptides exhibit markedly reduced capacity to cross link IgE and activate mast cells and basophils, due to lack of tertiary structure. Murine pre-clinical studies have established the feasibility of this approach and clinical studies are currently in progress in both allergic and autoimmune diseases. BioMed Central 2007-06-15 /pmc/articles/PMC2873623/ /pubmed/20525144 http://dx.doi.org/10.1186/1710-1492-3-2-53 Text en
spellingShingle Research
Larché, Mark
Immunotherapy with Allergen Peptides
title Immunotherapy with Allergen Peptides
title_full Immunotherapy with Allergen Peptides
title_fullStr Immunotherapy with Allergen Peptides
title_full_unstemmed Immunotherapy with Allergen Peptides
title_short Immunotherapy with Allergen Peptides
title_sort immunotherapy with allergen peptides
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873623/
https://www.ncbi.nlm.nih.gov/pubmed/20525144
http://dx.doi.org/10.1186/1710-1492-3-2-53
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