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Monoclonal Antibodies and Airway Diseases

Monoclonal antibodies, biologics, are a relatively new treatment option for severe chronic airway diseases, asthma, allergic rhinitis, and chronic rhinosinusitis (CRS). In this review, we focus on the physiological and pathomechanisms of monoclonal antibodies, and we present recent study results reg...

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Autores principales: Lyly, Annina, Laulajainen-Hongisto, Anu, Gevaert, Philippe, Kauppi, Paula, Toppila-Salmi, Sanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763928/
https://www.ncbi.nlm.nih.gov/pubmed/33322143
http://dx.doi.org/10.3390/ijms21249477
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author Lyly, Annina
Laulajainen-Hongisto, Anu
Gevaert, Philippe
Kauppi, Paula
Toppila-Salmi, Sanna
author_facet Lyly, Annina
Laulajainen-Hongisto, Anu
Gevaert, Philippe
Kauppi, Paula
Toppila-Salmi, Sanna
author_sort Lyly, Annina
collection PubMed
description Monoclonal antibodies, biologics, are a relatively new treatment option for severe chronic airway diseases, asthma, allergic rhinitis, and chronic rhinosinusitis (CRS). In this review, we focus on the physiological and pathomechanisms of monoclonal antibodies, and we present recent study results regarding their use as a therapeutic option against severe airway diseases. Airway mucosa acts as a relative barrier, modulating antigenic stimulation and responding to environmental pathogen exposure with a specific, self-limited response. In severe asthma and/or CRS, genome–environmental interactions lead to dysbiosis, aggravated inflammation, and disease. In healthy conditions, single or combined type 1, 2, and 3 immunological response pathways are invoked, generating cytokine, chemokine, innate cellular and T helper (Th) responses to eliminate viruses, helminths, and extracellular bacteria/fungi, correspondingly. Although the pathomechanisms are not fully known, the majority of severe airway diseases are related to type 2 high inflammation. Type 2 cytokines interleukins (IL) 4, 5, and 13, are orchestrated by innate lymphoid cell (ILC) and Th subsets leading to eosinophilia, immunoglobulin E (IgE) responses, and permanently impaired airway damage. Monoclonal antibodies can bind or block key parts of these inflammatory pathways, resulting in less inflammation and improved disease control.
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spelling pubmed-77639282020-12-27 Monoclonal Antibodies and Airway Diseases Lyly, Annina Laulajainen-Hongisto, Anu Gevaert, Philippe Kauppi, Paula Toppila-Salmi, Sanna Int J Mol Sci Review Monoclonal antibodies, biologics, are a relatively new treatment option for severe chronic airway diseases, asthma, allergic rhinitis, and chronic rhinosinusitis (CRS). In this review, we focus on the physiological and pathomechanisms of monoclonal antibodies, and we present recent study results regarding their use as a therapeutic option against severe airway diseases. Airway mucosa acts as a relative barrier, modulating antigenic stimulation and responding to environmental pathogen exposure with a specific, self-limited response. In severe asthma and/or CRS, genome–environmental interactions lead to dysbiosis, aggravated inflammation, and disease. In healthy conditions, single or combined type 1, 2, and 3 immunological response pathways are invoked, generating cytokine, chemokine, innate cellular and T helper (Th) responses to eliminate viruses, helminths, and extracellular bacteria/fungi, correspondingly. Although the pathomechanisms are not fully known, the majority of severe airway diseases are related to type 2 high inflammation. Type 2 cytokines interleukins (IL) 4, 5, and 13, are orchestrated by innate lymphoid cell (ILC) and Th subsets leading to eosinophilia, immunoglobulin E (IgE) responses, and permanently impaired airway damage. Monoclonal antibodies can bind or block key parts of these inflammatory pathways, resulting in less inflammation and improved disease control. MDPI 2020-12-13 /pmc/articles/PMC7763928/ /pubmed/33322143 http://dx.doi.org/10.3390/ijms21249477 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lyly, Annina
Laulajainen-Hongisto, Anu
Gevaert, Philippe
Kauppi, Paula
Toppila-Salmi, Sanna
Monoclonal Antibodies and Airway Diseases
title Monoclonal Antibodies and Airway Diseases
title_full Monoclonal Antibodies and Airway Diseases
title_fullStr Monoclonal Antibodies and Airway Diseases
title_full_unstemmed Monoclonal Antibodies and Airway Diseases
title_short Monoclonal Antibodies and Airway Diseases
title_sort monoclonal antibodies and airway diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763928/
https://www.ncbi.nlm.nih.gov/pubmed/33322143
http://dx.doi.org/10.3390/ijms21249477
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