Allergen immunotherapy: optimal duration for respiratory allergy
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Published version
Author(s)
Penagos Paniagua, Martin
Durham, Stephen R
Type
Journal Article
Abstract
Purpose of the Review: To analyse the evidence regarding the optimal duration of subcutaneous and sublingual immunotherapies to induce long-lasting benefits after treatment cessation for allergic rhinitis and asthma and to identify unmet needs.
Recent findings: Subcutaneous and sublingual immunotherapies are highly effective in desensitising selected subjects with allergic rhinitis and allergic asthma. Double-blind, placebo-controlled, randomised clinical trials of both routes of immunotherapy support international guidelines that recommend their use for at least three years to achieve disease modification and continued clinical and immunological tolerance for allergic rhinitis. Evidence of the long-term effects of allergen immunotherapy in the context of randomised controlled trials for allergic asthma as opposed to rhinitis is limited. Nonetheless, real-world studies suggest the long-lasting benefits of allergen immunotherapy for allergic asthma, as this reduces prescriptions for pharmacotherapy and decreases the risk of asthma exacerbations and hospitalisations. The GINA guideline 2023 recommends the use of house dust mite sublingual immunotherapy as an add-on therapy in subjects with suboptimally controlled asthma, despite the use of low to high doses of inhaled corticosteroids, provided that the FEV1 is >70% predicted.
Summary: Robust clinical trials of subcutaneous and sublingual immunotherapies have shown that 3 years of continuous treatment modifies the underlying course of allergic rhinitis with long-lasting clinical effects years after withdrawal. Further evaluations of the long-lasting effects of novel routes of allergen immunotherapy for allergic rhinitis and long-term studies for allergic asthma are needed in the context of randomised clinical trials.
Recent findings: Subcutaneous and sublingual immunotherapies are highly effective in desensitising selected subjects with allergic rhinitis and allergic asthma. Double-blind, placebo-controlled, randomised clinical trials of both routes of immunotherapy support international guidelines that recommend their use for at least three years to achieve disease modification and continued clinical and immunological tolerance for allergic rhinitis. Evidence of the long-term effects of allergen immunotherapy in the context of randomised controlled trials for allergic asthma as opposed to rhinitis is limited. Nonetheless, real-world studies suggest the long-lasting benefits of allergen immunotherapy for allergic asthma, as this reduces prescriptions for pharmacotherapy and decreases the risk of asthma exacerbations and hospitalisations. The GINA guideline 2023 recommends the use of house dust mite sublingual immunotherapy as an add-on therapy in subjects with suboptimally controlled asthma, despite the use of low to high doses of inhaled corticosteroids, provided that the FEV1 is >70% predicted.
Summary: Robust clinical trials of subcutaneous and sublingual immunotherapies have shown that 3 years of continuous treatment modifies the underlying course of allergic rhinitis with long-lasting clinical effects years after withdrawal. Further evaluations of the long-lasting effects of novel routes of allergen immunotherapy for allergic rhinitis and long-term studies for allergic asthma are needed in the context of randomised clinical trials.
Date Issued
2024-12
Date Acceptance
2024-09-30
Citation
Current Treatment Options in Allergy, 2024, 11 (4), pp.245-256
ISSN
2196-3053
Publisher
Springer
Start Page
245
End Page
256
Journal / Book Title
Current Treatment Options in Allergy
Volume
11
Issue
4
Copyright Statement
© The Author(s) 2024, corrected publication 2024 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
License URL
Identifier
https://link.springer.com/article/10.1007/s40521-024-00377-6
Publication Status
Published
Date Publish Online
2024-11-14