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Immunology of allergen immunotherapy

Allergen immunotherapy (AIT) is the only disease-modifying therapy for allergic disease. Through repeated inoculations of low doses of allergen—either as whole proteins or peptides—patients can achieve a homeostatic balance between inflammatory effectors induced and/or associated with allergen conta...

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Autores principales: Rahman, Rifat S, Wesemann, Duane R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749131/
https://www.ncbi.nlm.nih.gov/pubmed/36530352
http://dx.doi.org/10.1093/immadv/ltac022
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author Rahman, Rifat S
Wesemann, Duane R
author_facet Rahman, Rifat S
Wesemann, Duane R
author_sort Rahman, Rifat S
collection PubMed
description Allergen immunotherapy (AIT) is the only disease-modifying therapy for allergic disease. Through repeated inoculations of low doses of allergen—either as whole proteins or peptides—patients can achieve a homeostatic balance between inflammatory effectors induced and/or associated with allergen contact, and mediators of immunologic non-responsiveness, potentially leading to sustained clinical improvements. AIT for airborne/respiratory tract allergens and insect venoms have traditionally been supplied subcutaneously, but other routes and modalities of administration can also be effective. Despite differences of allergen administration, there are some similarities of immunologic responses across platforms, with a general theme involving the restructuring and polarization of adaptive and innate immune effector cells. Here we review the immunology of AIT across various delivery platforms, including subcutaneous, sublingual, epicutaneous, intradermal, and intralymphatic approaches, emphasizing shared mechanisms associated with achieving immunologic non-responsiveness to allergen.
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spelling pubmed-97491312022-12-15 Immunology of allergen immunotherapy Rahman, Rifat S Wesemann, Duane R Immunother Adv Review Allergen immunotherapy (AIT) is the only disease-modifying therapy for allergic disease. Through repeated inoculations of low doses of allergen—either as whole proteins or peptides—patients can achieve a homeostatic balance between inflammatory effectors induced and/or associated with allergen contact, and mediators of immunologic non-responsiveness, potentially leading to sustained clinical improvements. AIT for airborne/respiratory tract allergens and insect venoms have traditionally been supplied subcutaneously, but other routes and modalities of administration can also be effective. Despite differences of allergen administration, there are some similarities of immunologic responses across platforms, with a general theme involving the restructuring and polarization of adaptive and innate immune effector cells. Here we review the immunology of AIT across various delivery platforms, including subcutaneous, sublingual, epicutaneous, intradermal, and intralymphatic approaches, emphasizing shared mechanisms associated with achieving immunologic non-responsiveness to allergen. Oxford University Press 2022-11-25 /pmc/articles/PMC9749131/ /pubmed/36530352 http://dx.doi.org/10.1093/immadv/ltac022 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Rahman, Rifat S
Wesemann, Duane R
Immunology of allergen immunotherapy
title Immunology of allergen immunotherapy
title_full Immunology of allergen immunotherapy
title_fullStr Immunology of allergen immunotherapy
title_full_unstemmed Immunology of allergen immunotherapy
title_short Immunology of allergen immunotherapy
title_sort immunology of allergen immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749131/
https://www.ncbi.nlm.nih.gov/pubmed/36530352
http://dx.doi.org/10.1093/immadv/ltac022
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