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Benralizumab in the treatment of severe asthma: design, development and potential place in therapy
Asthma is a widespread and heterogeneous inflammatory disease of the airways, which is characterized by several different phenotypes and endotypes. In particular, eosinophilic airway inflammation is a common pathologic trait of both allergic and nonallergic asthma. The key cytokine responsible for m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868576/ https://www.ncbi.nlm.nih.gov/pubmed/29606855 http://dx.doi.org/10.2147/DDDT.S155307 |
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author | Pelaia, Corrado Vatrella, Alessandro Bruni, Andrea Terracciano, Rosa Pelaia, Girolamo |
author_facet | Pelaia, Corrado Vatrella, Alessandro Bruni, Andrea Terracciano, Rosa Pelaia, Girolamo |
author_sort | Pelaia, Corrado |
collection | PubMed |
description | Asthma is a widespread and heterogeneous inflammatory disease of the airways, which is characterized by several different phenotypes and endotypes. In particular, eosinophilic airway inflammation is a common pathologic trait of both allergic and nonallergic asthma. The key cytokine responsible for maturation, activation, recruitment, and survival of eosinophils is interleukin (IL)-5, which is mainly produced by T helper 2 (Th2) lymphocytes and group 2 innate lymphoid cells. Therefore, for uncontrolled patients with severe eosinophilic asthma, who are not fully responsive to corticosteroids, IL-5 represents a very important molecular target for add-on biological therapies. Among these new treatments, anti-IL-5 monoclonal antibodies such as mepolizumab and reslizumab have been developed and clinically evaluated. Furthermore, benralizumab is currently the only available biologic drug that specifically binds to the IL-5 receptor, thus preventing the interaction with its ligand and the consequent pro-inflammatory effects. The effectiveness of benralizumab in improving severe eosinophilic asthma has been well-documented by many randomized controlled trials. |
format | Online Article Text |
id | pubmed-5868576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58685762018-03-30 Benralizumab in the treatment of severe asthma: design, development and potential place in therapy Pelaia, Corrado Vatrella, Alessandro Bruni, Andrea Terracciano, Rosa Pelaia, Girolamo Drug Des Devel Ther Review Asthma is a widespread and heterogeneous inflammatory disease of the airways, which is characterized by several different phenotypes and endotypes. In particular, eosinophilic airway inflammation is a common pathologic trait of both allergic and nonallergic asthma. The key cytokine responsible for maturation, activation, recruitment, and survival of eosinophils is interleukin (IL)-5, which is mainly produced by T helper 2 (Th2) lymphocytes and group 2 innate lymphoid cells. Therefore, for uncontrolled patients with severe eosinophilic asthma, who are not fully responsive to corticosteroids, IL-5 represents a very important molecular target for add-on biological therapies. Among these new treatments, anti-IL-5 monoclonal antibodies such as mepolizumab and reslizumab have been developed and clinically evaluated. Furthermore, benralizumab is currently the only available biologic drug that specifically binds to the IL-5 receptor, thus preventing the interaction with its ligand and the consequent pro-inflammatory effects. The effectiveness of benralizumab in improving severe eosinophilic asthma has been well-documented by many randomized controlled trials. Dove Medical Press 2018-03-21 /pmc/articles/PMC5868576/ /pubmed/29606855 http://dx.doi.org/10.2147/DDDT.S155307 Text en © 2018 Pelaia et al. 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/). 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. |
spellingShingle | Review Pelaia, Corrado Vatrella, Alessandro Bruni, Andrea Terracciano, Rosa Pelaia, Girolamo Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title | Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title_full | Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title_fullStr | Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title_full_unstemmed | Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title_short | Benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
title_sort | benralizumab in the treatment of severe asthma: design, development and potential place in therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868576/ https://www.ncbi.nlm.nih.gov/pubmed/29606855 http://dx.doi.org/10.2147/DDDT.S155307 |
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