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Severe asthma: anti-IgE or anti-IL-5?
Severe asthma is a discrete clinical entity characterised by recurrent exacerbations, reduced quality of life and poor asthma control as ordinary treatment regimens remain inadequate. Difficulty in managing severe asthma derives partly from the multiple existing phenotypes and our inability to recog...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102127/ https://www.ncbi.nlm.nih.gov/pubmed/27834175 http://dx.doi.org/10.3402/ecrj.v3.31813 |
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author | Papathanassiou, Evgenia Loukides, Stelios Bakakos, Petros |
author_facet | Papathanassiou, Evgenia Loukides, Stelios Bakakos, Petros |
author_sort | Papathanassiou, Evgenia |
collection | PubMed |
description | Severe asthma is a discrete clinical entity characterised by recurrent exacerbations, reduced quality of life and poor asthma control as ordinary treatment regimens remain inadequate. Difficulty in managing severe asthma derives partly from the multiple existing phenotypes and our inability to recognise them. Though the exact pathogenetic pathway of severe allergic asthma remains unclear, it is known that numerous inflammatory cells and cytokines are involved, and eosinophils represent a key inflammatory cell mediator. Anti-IgE (omalizumab) and anti-IL-5 (mepolizumab) antibodies are biological agents that interfere in different steps of the Th2 inflammatory cascade and are licensed in severe asthma. Both exhibit a favourable clinical outcome as they reduce exacerbation rate and improve asthma control and quality of life, while mepolizumab also induces an oral steroid sparing effect. Nevertheless, it is still questionable which agent is more suitable in the management of severe allergic asthma since no comparable studies have been conducted. Omalizumab's established effectiveness in clinical practice over a long period is complemented by a beneficial effect on airway remodelling process mediated mainly through its impact on eosinophils and other parameters strongly related to eosinophilic inflammation. However, it is possible that mepolizumab through nearly depleting eosinophils could have a similar effect on airway remodelling. Moreover, to date, markers indicative of the patient population responding to each treatment are unavailable although baseline eosinophils and exacerbation rate in the previous year demonstrate a predictive value regarding anti-IL-5 therapy effectiveness. On the other hand, a better therapeutic response for omalizumab has been observed when low forced expiratory volume in 1 sec, high-dose inhaled corticosteroids and increased IgE concentrations are present. Consequently, conclusions are not yet safe to be drawn based on existing knowledge, and additional research is necessary to unravel the remaining issues for the severe asthmatic population. |
format | Online Article Text |
id | pubmed-5102127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-51021272016-11-18 Severe asthma: anti-IgE or anti-IL-5? Papathanassiou, Evgenia Loukides, Stelios Bakakos, Petros Eur Clin Respir J Review Article Severe asthma is a discrete clinical entity characterised by recurrent exacerbations, reduced quality of life and poor asthma control as ordinary treatment regimens remain inadequate. Difficulty in managing severe asthma derives partly from the multiple existing phenotypes and our inability to recognise them. Though the exact pathogenetic pathway of severe allergic asthma remains unclear, it is known that numerous inflammatory cells and cytokines are involved, and eosinophils represent a key inflammatory cell mediator. Anti-IgE (omalizumab) and anti-IL-5 (mepolizumab) antibodies are biological agents that interfere in different steps of the Th2 inflammatory cascade and are licensed in severe asthma. Both exhibit a favourable clinical outcome as they reduce exacerbation rate and improve asthma control and quality of life, while mepolizumab also induces an oral steroid sparing effect. Nevertheless, it is still questionable which agent is more suitable in the management of severe allergic asthma since no comparable studies have been conducted. Omalizumab's established effectiveness in clinical practice over a long period is complemented by a beneficial effect on airway remodelling process mediated mainly through its impact on eosinophils and other parameters strongly related to eosinophilic inflammation. However, it is possible that mepolizumab through nearly depleting eosinophils could have a similar effect on airway remodelling. Moreover, to date, markers indicative of the patient population responding to each treatment are unavailable although baseline eosinophils and exacerbation rate in the previous year demonstrate a predictive value regarding anti-IL-5 therapy effectiveness. On the other hand, a better therapeutic response for omalizumab has been observed when low forced expiratory volume in 1 sec, high-dose inhaled corticosteroids and increased IgE concentrations are present. Consequently, conclusions are not yet safe to be drawn based on existing knowledge, and additional research is necessary to unravel the remaining issues for the severe asthmatic population. Co-Action Publishing 2016-11-07 /pmc/articles/PMC5102127/ /pubmed/27834175 http://dx.doi.org/10.3402/ecrj.v3.31813 Text en © 2016 Evgenia Papathanassiou et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license. |
spellingShingle | Review Article Papathanassiou, Evgenia Loukides, Stelios Bakakos, Petros Severe asthma: anti-IgE or anti-IL-5? |
title | Severe asthma: anti-IgE or anti-IL-5? |
title_full | Severe asthma: anti-IgE or anti-IL-5? |
title_fullStr | Severe asthma: anti-IgE or anti-IL-5? |
title_full_unstemmed | Severe asthma: anti-IgE or anti-IL-5? |
title_short | Severe asthma: anti-IgE or anti-IL-5? |
title_sort | severe asthma: anti-ige or anti-il-5? |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102127/ https://www.ncbi.nlm.nih.gov/pubmed/27834175 http://dx.doi.org/10.3402/ecrj.v3.31813 |
work_keys_str_mv | AT papathanassiouevgenia severeasthmaantiigeorantiil5 AT loukidesstelios severeasthmaantiigeorantiil5 AT bakakospetros severeasthmaantiigeorantiil5 |