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Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study
The lungs have their own microbiota which seems to be altered in disease processes such as asthma. Viral infection accounts for many asthma exacerbations. Little is known about the lung virome, and the role that viruses play in non-exacerbating asthmatics. We aimed to assess if detection of virus in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186128/ https://www.ncbi.nlm.nih.gov/pubmed/37075793 http://dx.doi.org/10.4168/aair.2023.15.3.406 |
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author | Walsh, Laura J Sullivan, Ashley Ward, Christopher Fanning, Liam J O’Byrne, Paul M MacSharry, John A Murphy, Desmond M |
author_facet | Walsh, Laura J Sullivan, Ashley Ward, Christopher Fanning, Liam J O’Byrne, Paul M MacSharry, John A Murphy, Desmond M |
author_sort | Walsh, Laura J |
collection | PubMed |
description | The lungs have their own microbiota which seems to be altered in disease processes such as asthma. Viral infection accounts for many asthma exacerbations. Little is known about the lung virome, and the role that viruses play in non-exacerbating asthmatics. We aimed to assess if detection of virus in bronchoscopy samples of asthmatic patients in a non-exacerbating state influences their asthma control and modulates airway cytokine composition. Patients were recruited from a specialist asthma clinic and underwent bronchoscopy with standardised bronchoalveolar lavage (BAL). Viral analysis was performed; cell differential and cytokine levels were measured. Forty-six samples were obtained of which 10.8% demonstrated evidence of airway virus, and 91.3% of patients in the cohort were classed as severe asthmatics. Oral steroid use was significantly higher in severe asthmatic patients with virus detected, and the forced expiratory volume in one second tended to be lower in the virus-detected group. It was also found that BAL interleukin-13 and tumor necrosis factor-α levels were significantly higher in severe asthmatic patients with virus detected. Our results suggest that in severe asthmatics in a non-exacerbating state, the presence of virus resulted in overall poorer asthma control. The pattern of cytokine elevation seen in asthmatic patients with virus detected may provide insight to the pathophysiology involved. |
format | Online Article Text |
id | pubmed-10186128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease |
record_format | MEDLINE/PubMed |
spelling | pubmed-101861282023-05-17 Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study Walsh, Laura J Sullivan, Ashley Ward, Christopher Fanning, Liam J O’Byrne, Paul M MacSharry, John A Murphy, Desmond M Allergy Asthma Immunol Res Brief Communication The lungs have their own microbiota which seems to be altered in disease processes such as asthma. Viral infection accounts for many asthma exacerbations. Little is known about the lung virome, and the role that viruses play in non-exacerbating asthmatics. We aimed to assess if detection of virus in bronchoscopy samples of asthmatic patients in a non-exacerbating state influences their asthma control and modulates airway cytokine composition. Patients were recruited from a specialist asthma clinic and underwent bronchoscopy with standardised bronchoalveolar lavage (BAL). Viral analysis was performed; cell differential and cytokine levels were measured. Forty-six samples were obtained of which 10.8% demonstrated evidence of airway virus, and 91.3% of patients in the cohort were classed as severe asthmatics. Oral steroid use was significantly higher in severe asthmatic patients with virus detected, and the forced expiratory volume in one second tended to be lower in the virus-detected group. It was also found that BAL interleukin-13 and tumor necrosis factor-α levels were significantly higher in severe asthmatic patients with virus detected. Our results suggest that in severe asthmatics in a non-exacerbating state, the presence of virus resulted in overall poorer asthma control. The pattern of cytokine elevation seen in asthmatic patients with virus detected may provide insight to the pathophysiology involved. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2023-01-09 /pmc/articles/PMC10186128/ /pubmed/37075793 http://dx.doi.org/10.4168/aair.2023.15.3.406 Text en Copyright © 2023 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communication Walsh, Laura J Sullivan, Ashley Ward, Christopher Fanning, Liam J O’Byrne, Paul M MacSharry, John A Murphy, Desmond M Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title | Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title_full | Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title_fullStr | Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title_full_unstemmed | Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title_short | Impact of Airway Virus in Severe Asthmatic Patients: A Pilot Study |
title_sort | impact of airway virus in severe asthmatic patients: a pilot study |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186128/ https://www.ncbi.nlm.nih.gov/pubmed/37075793 http://dx.doi.org/10.4168/aair.2023.15.3.406 |
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