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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7763928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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