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Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma
Asthma is a very frequent chronic airway disease that includes many different clinical phenotypes and inflammatory patterns. In particular, eosinophilic bronchial inflammation is often associated with allergic as well as nonallergic asthma. The most important cytokine involved in the induction, main...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971345/ https://www.ncbi.nlm.nih.gov/pubmed/29862274 http://dx.doi.org/10.1155/2018/4839230 |
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author | Pelaia, Corrado Calabrese, Cecilia Vatrella, Alessandro Busceti, Maria Teresa Garofalo, Eugenio Lombardo, Nicola Terracciano, Rosa Pelaia, Girolamo |
author_facet | Pelaia, Corrado Calabrese, Cecilia Vatrella, Alessandro Busceti, Maria Teresa Garofalo, Eugenio Lombardo, Nicola Terracciano, Rosa Pelaia, Girolamo |
author_sort | Pelaia, Corrado |
collection | PubMed |
description | Asthma is a very frequent chronic airway disease that includes many different clinical phenotypes and inflammatory patterns. In particular, eosinophilic bronchial inflammation is often associated with allergic as well as nonallergic asthma. The most important cytokine involved in the induction, maintenance, and amplification of airway eosinophilia in asthma is interleukin-5 (IL-5), released by both T helper 2 (Th2) lymphocytes and group 2 innate lymphoid cells (ILC2). Hence, IL-5 and its receptor are suitable targets for selective biologic drugs which can play a key role in add-on treatment of severe eosinophilic asthma refractory to corticosteroids. Within such a context, the anti-IL-5 monoclonal antibodies mepolizumab and reslizumab have been developed and approved for biological therapy of uncontrolled eosinophilic asthma. In this regard, on the basis of several successful randomized controlled trials, the anti-IL-5 receptor benralizumab has also recently obtained the approval from US Food and Drug Administration (FDA). |
format | Online Article Text |
id | pubmed-5971345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-59713452018-06-03 Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma Pelaia, Corrado Calabrese, Cecilia Vatrella, Alessandro Busceti, Maria Teresa Garofalo, Eugenio Lombardo, Nicola Terracciano, Rosa Pelaia, Girolamo Biomed Res Int Review Article Asthma is a very frequent chronic airway disease that includes many different clinical phenotypes and inflammatory patterns. In particular, eosinophilic bronchial inflammation is often associated with allergic as well as nonallergic asthma. The most important cytokine involved in the induction, maintenance, and amplification of airway eosinophilia in asthma is interleukin-5 (IL-5), released by both T helper 2 (Th2) lymphocytes and group 2 innate lymphoid cells (ILC2). Hence, IL-5 and its receptor are suitable targets for selective biologic drugs which can play a key role in add-on treatment of severe eosinophilic asthma refractory to corticosteroids. Within such a context, the anti-IL-5 monoclonal antibodies mepolizumab and reslizumab have been developed and approved for biological therapy of uncontrolled eosinophilic asthma. In this regard, on the basis of several successful randomized controlled trials, the anti-IL-5 receptor benralizumab has also recently obtained the approval from US Food and Drug Administration (FDA). Hindawi 2018-05-10 /pmc/articles/PMC5971345/ /pubmed/29862274 http://dx.doi.org/10.1155/2018/4839230 Text en Copyright © 2018 Corrado Pelaia et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Pelaia, Corrado Calabrese, Cecilia Vatrella, Alessandro Busceti, Maria Teresa Garofalo, Eugenio Lombardo, Nicola Terracciano, Rosa Pelaia, Girolamo Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title | Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title_full | Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title_fullStr | Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title_full_unstemmed | Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title_short | Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma |
title_sort | benralizumab: from the basic mechanism of action to the potential use in the biological therapy of severe eosinophilic asthma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971345/ https://www.ncbi.nlm.nih.gov/pubmed/29862274 http://dx.doi.org/10.1155/2018/4839230 |
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