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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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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. |
format | Text |
id | pubmed-2873623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT larchemark immunotherapywithallergenpeptides |