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Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review

BACKGROUND: Airway hyperresponsiveness (AHR) is a key feature of asthma. Biologic therapies used to treat asthma target specific components of the inflammatory pathway, and their effects on AHR can provide valuable information about the underlying disease pathophysiology. This review summarizes the...

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Autores principales: Spahn, Joseph D, Brightling, Christopher E, O’Byrne, Paul M, Simpson, Lisa J, Molfino, Nestor A, Ambrose, Christopher S, Martin, Neil, Hallstrand, Teal S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368134/
https://www.ncbi.nlm.nih.gov/pubmed/37496824
http://dx.doi.org/10.2147/JAA.S410592
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author Spahn, Joseph D
Brightling, Christopher E
O’Byrne, Paul M
Simpson, Lisa J
Molfino, Nestor A
Ambrose, Christopher S
Martin, Neil
Hallstrand, Teal S
author_facet Spahn, Joseph D
Brightling, Christopher E
O’Byrne, Paul M
Simpson, Lisa J
Molfino, Nestor A
Ambrose, Christopher S
Martin, Neil
Hallstrand, Teal S
author_sort Spahn, Joseph D
collection PubMed
description BACKGROUND: Airway hyperresponsiveness (AHR) is a key feature of asthma. Biologic therapies used to treat asthma target specific components of the inflammatory pathway, and their effects on AHR can provide valuable information about the underlying disease pathophysiology. This review summarizes the available evidence regarding the effects of biologics on allergen-specific and non-allergen-specific airway responses in patients with asthma. METHODS: We conducted a systematic review in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines, including risk-of-bias assessment. PubMed and Ovid were searched for studies published between January 1997 and December 2021. Eligible studies were randomized, placebo-controlled trials that assessed the effects of biologics on AHR, early allergic response (EAR) and/or late allergic response (LAR) in patients with asthma. RESULTS: Thirty studies were identified for inclusion. Bronchoprovocation testing was allergen-specific in 18 studies and non-allergen-specific in 12 studies. Omalizumab reduced AHR to methacholine, acetylcholine or adenosine monophosphate (3/9 studies), and reduced EAR (4/5 studies) and LAR (2/3 studies). Mepolizumab had no effect on AHR (3/3 studies), EAR or LAR (1/1 study). Tezepelumab reduced AHR to methacholine or mannitol (3/3 studies), and reduced EAR and LAR (1/1 study). Pitrakinra reduced LAR, with no effect on AHR (1/1 study). Etanercept reduced AHR to methacholine (1/2 studies). No effects were observed for lebrikizumab, tocilizumab, efalizumab, IMA-638 and anti-OX40 ligand on AHR, EAR or LAR; benralizumab on LAR; tralokinumab on AHR; and Ro-24-7472 on AHR or LAR (all 1/1 study each). No dupilumab or reslizumab studies were identified. CONCLUSION: Omalizumab and tezepelumab reduced EAR and LAR to allergens. Tezepelumab consistently reduced AHR to methacholine or mannitol. These findings provide insights into AHR mechanisms and the precise effects of asthma biologics. Furthermore, findings suggest that tezepelumab broadly targets allergen-specific and non-allergic forms of AHR, and the underlying cells and mediators involved in asthma.
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spelling pubmed-103681342023-07-26 Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review Spahn, Joseph D Brightling, Christopher E O’Byrne, Paul M Simpson, Lisa J Molfino, Nestor A Ambrose, Christopher S Martin, Neil Hallstrand, Teal S J Asthma Allergy Review BACKGROUND: Airway hyperresponsiveness (AHR) is a key feature of asthma. Biologic therapies used to treat asthma target specific components of the inflammatory pathway, and their effects on AHR can provide valuable information about the underlying disease pathophysiology. This review summarizes the available evidence regarding the effects of biologics on allergen-specific and non-allergen-specific airway responses in patients with asthma. METHODS: We conducted a systematic review in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines, including risk-of-bias assessment. PubMed and Ovid were searched for studies published between January 1997 and December 2021. Eligible studies were randomized, placebo-controlled trials that assessed the effects of biologics on AHR, early allergic response (EAR) and/or late allergic response (LAR) in patients with asthma. RESULTS: Thirty studies were identified for inclusion. Bronchoprovocation testing was allergen-specific in 18 studies and non-allergen-specific in 12 studies. Omalizumab reduced AHR to methacholine, acetylcholine or adenosine monophosphate (3/9 studies), and reduced EAR (4/5 studies) and LAR (2/3 studies). Mepolizumab had no effect on AHR (3/3 studies), EAR or LAR (1/1 study). Tezepelumab reduced AHR to methacholine or mannitol (3/3 studies), and reduced EAR and LAR (1/1 study). Pitrakinra reduced LAR, with no effect on AHR (1/1 study). Etanercept reduced AHR to methacholine (1/2 studies). No effects were observed for lebrikizumab, tocilizumab, efalizumab, IMA-638 and anti-OX40 ligand on AHR, EAR or LAR; benralizumab on LAR; tralokinumab on AHR; and Ro-24-7472 on AHR or LAR (all 1/1 study each). No dupilumab or reslizumab studies were identified. CONCLUSION: Omalizumab and tezepelumab reduced EAR and LAR to allergens. Tezepelumab consistently reduced AHR to methacholine or mannitol. These findings provide insights into AHR mechanisms and the precise effects of asthma biologics. Furthermore, findings suggest that tezepelumab broadly targets allergen-specific and non-allergic forms of AHR, and the underlying cells and mediators involved in asthma. Dove 2023-07-21 /pmc/articles/PMC10368134/ /pubmed/37496824 http://dx.doi.org/10.2147/JAA.S410592 Text en © 2023 Spahn et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Spahn, Joseph D
Brightling, Christopher E
O’Byrne, Paul M
Simpson, Lisa J
Molfino, Nestor A
Ambrose, Christopher S
Martin, Neil
Hallstrand, Teal S
Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title_full Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title_fullStr Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title_full_unstemmed Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title_short Effect of Biologic Therapies on Airway Hyperresponsiveness and Allergic Response: A Systematic Literature Review
title_sort effect of biologic therapies on airway hyperresponsiveness and allergic response: a systematic literature review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368134/
https://www.ncbi.nlm.nih.gov/pubmed/37496824
http://dx.doi.org/10.2147/JAA.S410592
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