Evidence map›Paper›PMID 31400236›Full record

Trial reportClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology2019

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

Abilash Ravi, Meiping Chang, Marianne van de Pol, Shan Yang, Antonios Aliprantis, Bob Thornton, Leonidas N Carayannopoulos, An Bautmans, Martine Robberechts, Inge De Lepeleire and 6 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Rhinovirus-16 induced temporal interferon responses in nasal epithelium links with viral clearance and symptoms.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2019
    Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Article
  13. Review
  14. Does Trypsin Oral Spray (ViruprotectInternational journal of environmental research and public health · 2021
    Article
  15. Article
  16. Article
  17. Mechanism of Rhinovirus Immunity and Asthma.Frontiers in immunology · 2021
    Review
  18. Vaping and Respiratory Viruses: The End for ENDS?American journal of respiratory cell and molecular biology · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 5 countries.

Abilash RaviAmsterdam UMC, Department of Respiratory Medicine, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-7502-7115
Meiping ChangMerck & Co., Inc., Kenilworth, NJ, USA.
Marianne van de PolAmsterdam UMC, Department of Respiratory Medicine, University of Amsterdam, Amsterdam, The Netherlands.
Shan YangMerck & Co., Inc., Kenilworth, NJ, USA.
Antonios AliprantisMerck & Co., Inc., Kenilworth, NJ, USA.
Bob ThorntonMerck & Co., Inc., Kenilworth, NJ, USA.
Leonidas N CarayannopoulosMerck & Co., Inc., Kenilworth, NJ, USA.
An BautmansMerck Sharp and Dohme, Europe Inc., Brussels, Belgium.
Martine RobberechtsMerck Sharp and Dohme, Europe Inc., Brussels, Belgium.
Inge De LepeleireMerck Sharp and Dohme, Europe Inc., Brussels, Belgium.
Dave SinghDivision of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, UK.
Jens M HohlfeldFraunhofer Institute for Toxicology and Experimental Medicine, Hannover, Germany.
Peter J SterkAmsterdam UMC, Department of Respiratory Medicine, University of Amsterdam, Amsterdam, The Netherlands.
Norbert KrugFraunhofer Institute for Toxicology and Experimental Medicine, Hannover, Germany.
René LutterAmsterdam UMC, Department of Respiratory Medicine, University of Amsterdam, Amsterdam, The Netherlands.
U-BIOPRED Study Group
Merck & Co., Inc., Rahway, NJ, USA (United States) · USAmsterdam University Medical Centers · NLMSD (Belgium) · BEFraunhofer Institute for Toxicology and Experimental Medicine · DEUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

objectiveTo 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.

methodsPatients 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.

resultsTop 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.

Indexed as

AsthmaBronchiNasal MucosaPicornaviridae InfectionsAdultFemaleHumansInterferon-alphaInterferon-gammaMaleMiddle AgedRhinovirusIFNG protein, humanInterferon-alphaInterferon-gammaasthmaepitheliuminnate immunityinterferon responsenasal epitheliumrhinovirusvirus

Identifiers

PMID31400236
PMCPMC6972523
OpenAlexW2967915363

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.