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Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring

BACKGROUND: With the clinical development of several antiviral intervention strategies for influenza, it becomes crucial to explore viral load shedding in the nasal cavity as a biomarker for treatment success, but also to explore sampling strategies for sensible and reliable virus collection. FINDIN...

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Autores principales: Van Wesenbeeck, Liesbeth, Meeuws, Hanne, D’Haese, David, Ispas, Gabriela, Houspie, Lieselot, Van Ranst, Marc, Stuyver, Lieven J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304201/
https://www.ncbi.nlm.nih.gov/pubmed/25539740
http://dx.doi.org/10.1186/s12985-014-0233-9
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author Van Wesenbeeck, Liesbeth
Meeuws, Hanne
D’Haese, David
Ispas, Gabriela
Houspie, Lieselot
Van Ranst, Marc
Stuyver, Lieven J
author_facet Van Wesenbeeck, Liesbeth
Meeuws, Hanne
D’Haese, David
Ispas, Gabriela
Houspie, Lieselot
Van Ranst, Marc
Stuyver, Lieven J
author_sort Van Wesenbeeck, Liesbeth
collection PubMed
description BACKGROUND: With the clinical development of several antiviral intervention strategies for influenza, it becomes crucial to explore viral load shedding in the nasal cavity as a biomarker for treatment success, but also to explore sampling strategies for sensible and reliable virus collection. FINDINGS: In this study, 244 patients suffering from Influenza like Illness and/or acute respiratory tract infection were enrolled. Sampling was done using mid-turbinate flocked swabs and two swabs per patient were collected (one swab per nostril). The influenza A viral loads of two mid-turbinate flocked swabs (one for each nostril) per patient were compared and we have also assessed whether normalization for human cellular DNA in the swabs could be useful. The Influenza mid-turbinate nasal swab testing resulted in considerable sampling variability that could not be normalized against co-isolated human cellular DNA. CONCLUSIONS: Influenza viral load monitoring in nasal swabs could be very valuable as virological endpoints in clinical trials to monitor treatment efficacy, in analogy to HIV, HBV & HCV viral load monitoring. However, the differences between left and right nostrils, as observed in this study, highlight the importance of proper sampling and the need for standardized sampling procedures.
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spelling pubmed-43042012015-01-24 Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring Van Wesenbeeck, Liesbeth Meeuws, Hanne D’Haese, David Ispas, Gabriela Houspie, Lieselot Van Ranst, Marc Stuyver, Lieven J Virol J Short Report BACKGROUND: With the clinical development of several antiviral intervention strategies for influenza, it becomes crucial to explore viral load shedding in the nasal cavity as a biomarker for treatment success, but also to explore sampling strategies for sensible and reliable virus collection. FINDINGS: In this study, 244 patients suffering from Influenza like Illness and/or acute respiratory tract infection were enrolled. Sampling was done using mid-turbinate flocked swabs and two swabs per patient were collected (one swab per nostril). The influenza A viral loads of two mid-turbinate flocked swabs (one for each nostril) per patient were compared and we have also assessed whether normalization for human cellular DNA in the swabs could be useful. The Influenza mid-turbinate nasal swab testing resulted in considerable sampling variability that could not be normalized against co-isolated human cellular DNA. CONCLUSIONS: Influenza viral load monitoring in nasal swabs could be very valuable as virological endpoints in clinical trials to monitor treatment efficacy, in analogy to HIV, HBV & HCV viral load monitoring. However, the differences between left and right nostrils, as observed in this study, highlight the importance of proper sampling and the need for standardized sampling procedures. BioMed Central 2014-12-24 /pmc/articles/PMC4304201/ /pubmed/25539740 http://dx.doi.org/10.1186/s12985-014-0233-9 Text en © Van Wesenbeeck et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Van Wesenbeeck, Liesbeth
Meeuws, Hanne
D’Haese, David
Ispas, Gabriela
Houspie, Lieselot
Van Ranst, Marc
Stuyver, Lieven J
Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title_full Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title_fullStr Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title_full_unstemmed Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title_short Sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
title_sort sampling variability between two mid-turbinate swabs of the same patient has implications for influenza viral load monitoring
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304201/
https://www.ncbi.nlm.nih.gov/pubmed/25539740
http://dx.doi.org/10.1186/s12985-014-0233-9
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