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Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms

BACKGROUND: The temporal in vivo response of epithelial cells to a viral challenge and its association with viral clearance and clinical outcomes has been largely unexplored in asthma. OBJECTIVE: To determine gene expression profiles over time in nasal epithelial cells (NECs) challenged in vivo with...

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Autores principales: Ravi, Abilash, Chang, Meiping, van de Pol, Marianne, Yang, Shan, Aliprantis, Antonios, Thornton, Bob, Carayannopoulos, Leonidas N., Bautmans, An, Robberechts, Martine, De Lepeleire, Inge, Singh, Dave, Hohlfeld, Jens M., Sterk, Peter J., Krug, Norbert, Lutter, René
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972523/
https://www.ncbi.nlm.nih.gov/pubmed/31400236
http://dx.doi.org/10.1111/cea.13481
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author Ravi, Abilash
Chang, Meiping
van de Pol, Marianne
Yang, Shan
Aliprantis, Antonios
Thornton, Bob
Carayannopoulos, Leonidas N.
Bautmans, An
Robberechts, Martine
De Lepeleire, Inge
Singh, Dave
Hohlfeld, Jens M.
Sterk, Peter J.
Krug, Norbert
Lutter, René
author_facet Ravi, Abilash
Chang, Meiping
van de Pol, Marianne
Yang, Shan
Aliprantis, Antonios
Thornton, Bob
Carayannopoulos, Leonidas N.
Bautmans, An
Robberechts, Martine
De Lepeleire, Inge
Singh, Dave
Hohlfeld, Jens M.
Sterk, Peter J.
Krug, Norbert
Lutter, René
author_sort Ravi, Abilash
collection PubMed
description BACKGROUND: The temporal in vivo response of epithelial cells to a viral challenge and its association with viral clearance and clinical outcomes has been largely unexplored in asthma. OBJECTIVE: To determine gene expression profiles over time in nasal epithelial cells (NECs) challenged in vivo with rhinovirus‐16 (RV16) and compare to nasal symptoms and viral clearance. METHODS: Patients with stable mild to moderate asthma (n = 20) were challenged intranasally with RV16. Nasal brush samples for RNA sequencing were taken 7 days prior to infection and 3, 6 and 14 days post‐infection, and blood samples 4 days prior to infection and day 6 post‐infection. Viral load was measured in nasal lavage fluid at day 3, 6 and 14. RESULTS: Top differentially (>2.5‐fold increase) expressed gene sets in NECs post‐RV16 at days 3 and 6, compared with baseline, were interferon alpha and gamma response genes. Patients clearing the virus within 6 days (early resolvers) had a significantly increased interferon response at day 6, whereas those having cleared the virus by day 14 (late resolvers) had significantly increased responses at day 3, 6 and 14. Interestingly, patients not having cleared the virus by day 14 (non‐resolvers) had no enhanced interferon responses at any of these days. The daily Cold Symptom Scores (CSS) peaked at days 3 to 5 and correlated positively with interferon response genes at day 3 (R = 0.48), but not at other time‐points. Interferon response genes were also enhanced in blood at day 6 after RV16 challenge. CONCLUSION AND CLINICAL RELEVANCE: This study shows that viral load and clearance varies markedly over time in mild to moderate asthma patients exposed to a fixed RV16 dose. The host's nasal interferon response to RV16 at day 3 is associated with upper respiratory tract symptoms. The temporal interferon response in nasal epithelium associates with viral clearance in the nasal compartment.
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spelling pubmed-69725232020-01-27 Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms Ravi, Abilash Chang, Meiping van de Pol, Marianne Yang, Shan Aliprantis, Antonios Thornton, Bob Carayannopoulos, Leonidas N. Bautmans, An Robberechts, Martine De Lepeleire, Inge Singh, Dave Hohlfeld, Jens M. Sterk, Peter J. Krug, Norbert Lutter, René Clin Exp Allergy ORIGINAL ARTICLES BACKGROUND: The temporal in vivo response of epithelial cells to a viral challenge and its association with viral clearance and clinical outcomes has been largely unexplored in asthma. OBJECTIVE: To determine gene expression profiles over time in nasal epithelial cells (NECs) challenged in vivo with rhinovirus‐16 (RV16) and compare to nasal symptoms and viral clearance. METHODS: Patients with stable mild to moderate asthma (n = 20) were challenged intranasally with RV16. Nasal brush samples for RNA sequencing were taken 7 days prior to infection and 3, 6 and 14 days post‐infection, and blood samples 4 days prior to infection and day 6 post‐infection. Viral load was measured in nasal lavage fluid at day 3, 6 and 14. RESULTS: Top differentially (>2.5‐fold increase) expressed gene sets in NECs post‐RV16 at days 3 and 6, compared with baseline, were interferon alpha and gamma response genes. Patients clearing the virus within 6 days (early resolvers) had a significantly increased interferon response at day 6, whereas those having cleared the virus by day 14 (late resolvers) had significantly increased responses at day 3, 6 and 14. Interestingly, patients not having cleared the virus by day 14 (non‐resolvers) had no enhanced interferon responses at any of these days. The daily Cold Symptom Scores (CSS) peaked at days 3 to 5 and correlated positively with interferon response genes at day 3 (R = 0.48), but not at other time‐points. Interferon response genes were also enhanced in blood at day 6 after RV16 challenge. CONCLUSION AND CLINICAL RELEVANCE: This study shows that viral load and clearance varies markedly over time in mild to moderate asthma patients exposed to a fixed RV16 dose. The host's nasal interferon response to RV16 at day 3 is associated with upper respiratory tract symptoms. The temporal interferon response in nasal epithelium associates with viral clearance in the nasal compartment. John Wiley and Sons Inc. 2019-10-31 2019-12 /pmc/articles/PMC6972523/ /pubmed/31400236 http://dx.doi.org/10.1111/cea.13481 Text en © 2019 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ORIGINAL ARTICLES
Ravi, Abilash
Chang, Meiping
van de Pol, Marianne
Yang, Shan
Aliprantis, Antonios
Thornton, Bob
Carayannopoulos, Leonidas N.
Bautmans, An
Robberechts, Martine
De Lepeleire, Inge
Singh, Dave
Hohlfeld, Jens M.
Sterk, Peter J.
Krug, Norbert
Lutter, René
Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title_full Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title_fullStr Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title_full_unstemmed Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title_short Rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
title_sort rhinovirus‐16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972523/
https://www.ncbi.nlm.nih.gov/pubmed/31400236
http://dx.doi.org/10.1111/cea.13481
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