Forskning
Udskriv Udskriv
Switch language
Region Hovedstaden - en del af Københavns Universitetshospital
Udgivet

Treating severe asthma: targeting the IL-5 pathway

Publikation: Bidrag til tidsskriftReviewForskningpeer review

Harvard

Principe, S, Porsbjerg, C, Bolm Ditlev, S, Kjaersgaard Klein, D, Golebski, K, Dyhre-Petersen, N, van Dijk, YE, van Bragt, JJMH, Dankelman, LLH, Dahlen, S-E, Brightling, CE, Vijverberg, SJH & Maitland-van der Zee, AH 2021, 'Treating severe asthma: targeting the IL-5 pathway', Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, bind 51, nr. 8, s. 992-1005. https://doi.org/10.1111/cea.13885

APA

Principe, S., Porsbjerg, C., Bolm Ditlev, S., Kjaersgaard Klein, D., Golebski, K., Dyhre-Petersen, N., van Dijk, Y. E., van Bragt, J. J. M. H., Dankelman, L. L. H., Dahlen, S-E., Brightling, C. E., Vijverberg, S. J. H., & Maitland-van der Zee, A. H. (2021). Treating severe asthma: targeting the IL-5 pathway. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 51(8), 992-1005. https://doi.org/10.1111/cea.13885

CBE

Principe S, Porsbjerg C, Bolm Ditlev S, Kjaersgaard Klein D, Golebski K, Dyhre-Petersen N, van Dijk YE, van Bragt JJMH, Dankelman LLH, Dahlen S-E, Brightling CE, Vijverberg SJH, Maitland-van der Zee AH. 2021. Treating severe asthma: targeting the IL-5 pathway. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 51(8):992-1005. https://doi.org/10.1111/cea.13885

MLA

Vancouver

Author

Principe, Stefania ; Porsbjerg, Celeste ; Bolm Ditlev, Sisse ; Kjaersgaard Klein, Ditte ; Golebski, Korneliusz ; Dyhre-Petersen, Nanna ; van Dijk, Yoni E ; van Bragt, Job J M H ; Dankelman, Lente L H ; Dahlen, Sven-Erik ; Brightling, Christopher E ; Vijverberg, Susanne J H ; Maitland-van der Zee, Anke H. / Treating severe asthma : targeting the IL-5 pathway. I: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2021 ; Bind 51, Nr. 8. s. 992-1005.

Bibtex

@article{80ea69b64b97400aa49be5e7dc6d5eb3,
title = "Treating severe asthma: targeting the IL-5 pathway",
abstract = "Severe asthma is a heterogeneous disease with different phenotypes based on clinical, functional or inflammatory parameters. In particular, the eosinophilic phenotype is associated with type 2 inflammation and increased levels of interleukin (IL)-4, IL-5 and IL-13). Monoclonal antibodies that target the eosinophilic inflammatory pathways (IL-5R and IL-5), namely mepolizumab, reslizumab, and benralizumab, are effective and safe for severe eosinophilic asthma. Eosinophils threshold represents the most indicative biomarker for response to treatment with all three monoclonal antibodies. Improvement in asthma symptoms scores, lung function, the number of exacerbations, history of late-onset asthma, chronic rhinosinusitis with nasal polyposis, low oral corticosteroids use and low body mass index represent predictive clinical markers of response. Novel Omics studies are emerging with proteomics data and exhaled breath analyses. These may prove useful as biomarkers of response and non-response biologics. Moreover, future biomarker studies need to be undertaken in paediatric patients affected by severe asthma. The choice of appropriate biologic therapy for severe asthma remains challenging. The importance of finding biomarkers that can predict response continuous an open issue that needs to be further explored. This review describes the clinical effects of targeting the IL-5 pathway in severe asthma in adult and paediatric patients, focusing on predictors of response and non-response.",
author = "Stefania Principe and Celeste Porsbjerg and {Bolm Ditlev}, Sisse and {Kjaersgaard Klein}, Ditte and Korneliusz Golebski and Nanna Dyhre-Petersen and {van Dijk}, {Yoni E} and {van Bragt}, {Job J M H} and Dankelman, {Lente L H} and Sven-Erik Dahlen and Brightling, {Christopher E} and Vijverberg, {Susanne J H} and {Maitland-van der Zee}, {Anke H}",
note = "This article is protected by copyright. All rights reserved.",
year = "2021",
month = aug,
doi = "10.1111/cea.13885",
language = "English",
volume = "51",
pages = "992--1005",
journal = "Clinical Allergy",
issn = "0954-7894",
publisher = "Wiley-Blackwell Publishing Ltd",
number = "8",

}

RIS

TY - JOUR

T1 - Treating severe asthma

T2 - targeting the IL-5 pathway

AU - Principe, Stefania

AU - Porsbjerg, Celeste

AU - Bolm Ditlev, Sisse

AU - Kjaersgaard Klein, Ditte

AU - Golebski, Korneliusz

AU - Dyhre-Petersen, Nanna

AU - van Dijk, Yoni E

AU - van Bragt, Job J M H

AU - Dankelman, Lente L H

AU - Dahlen, Sven-Erik

AU - Brightling, Christopher E

AU - Vijverberg, Susanne J H

AU - Maitland-van der Zee, Anke H

N1 - This article is protected by copyright. All rights reserved.

PY - 2021/8

Y1 - 2021/8

N2 - Severe asthma is a heterogeneous disease with different phenotypes based on clinical, functional or inflammatory parameters. In particular, the eosinophilic phenotype is associated with type 2 inflammation and increased levels of interleukin (IL)-4, IL-5 and IL-13). Monoclonal antibodies that target the eosinophilic inflammatory pathways (IL-5R and IL-5), namely mepolizumab, reslizumab, and benralizumab, are effective and safe for severe eosinophilic asthma. Eosinophils threshold represents the most indicative biomarker for response to treatment with all three monoclonal antibodies. Improvement in asthma symptoms scores, lung function, the number of exacerbations, history of late-onset asthma, chronic rhinosinusitis with nasal polyposis, low oral corticosteroids use and low body mass index represent predictive clinical markers of response. Novel Omics studies are emerging with proteomics data and exhaled breath analyses. These may prove useful as biomarkers of response and non-response biologics. Moreover, future biomarker studies need to be undertaken in paediatric patients affected by severe asthma. The choice of appropriate biologic therapy for severe asthma remains challenging. The importance of finding biomarkers that can predict response continuous an open issue that needs to be further explored. This review describes the clinical effects of targeting the IL-5 pathway in severe asthma in adult and paediatric patients, focusing on predictors of response and non-response.

AB - Severe asthma is a heterogeneous disease with different phenotypes based on clinical, functional or inflammatory parameters. In particular, the eosinophilic phenotype is associated with type 2 inflammation and increased levels of interleukin (IL)-4, IL-5 and IL-13). Monoclonal antibodies that target the eosinophilic inflammatory pathways (IL-5R and IL-5), namely mepolizumab, reslizumab, and benralizumab, are effective and safe for severe eosinophilic asthma. Eosinophils threshold represents the most indicative biomarker for response to treatment with all three monoclonal antibodies. Improvement in asthma symptoms scores, lung function, the number of exacerbations, history of late-onset asthma, chronic rhinosinusitis with nasal polyposis, low oral corticosteroids use and low body mass index represent predictive clinical markers of response. Novel Omics studies are emerging with proteomics data and exhaled breath analyses. These may prove useful as biomarkers of response and non-response biologics. Moreover, future biomarker studies need to be undertaken in paediatric patients affected by severe asthma. The choice of appropriate biologic therapy for severe asthma remains challenging. The importance of finding biomarkers that can predict response continuous an open issue that needs to be further explored. This review describes the clinical effects of targeting the IL-5 pathway in severe asthma in adult and paediatric patients, focusing on predictors of response and non-response.

UR - http://www.scopus.com/inward/record.url?scp=85106256361&partnerID=8YFLogxK

U2 - 10.1111/cea.13885

DO - 10.1111/cea.13885

M3 - Review

C2 - 33887082

VL - 51

SP - 992

EP - 1005

JO - Clinical Allergy

JF - Clinical Allergy

SN - 0954-7894

IS - 8

ER -

ID: 65066147