Evidence map›Paper›PMID 29029245›Full record

ArticleThe Journal of infectious diseases2017

Host Transcription Profile in Nasal Epithelium and Whole Blood of Hospitalized Children Under 2 Years of Age With Respiratory Syncytial Virus Infection.

Lien Anh Ha Do, Johann Pellet, H Rogier van Doorn, Anh Tuan Tran, Bach Hue Nguyen, Thi Thu Loan Tran, Quynh Huong Tran, Quoc Bao Vo, Nguyen Anh Tran Dac, Hong Nhien Trinh and 18 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Age-related Differences in the Nasal Mucosal Immune Response to SARS-CoV-2.American journal of respiratory cell and molecular biology · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Immune response to SARS-CoV-2 in the nasal mucosa in children and adults.medRxiv : the preprint server for health sciences · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Infant Immune Response to Respiratory Viral Infections.Immunology and allergy clinics of North America · 2019
    Review
  19. Article
  20. Review
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

28 authors at 7 institutions in 5 countries.

Lien Anh Ha DoOxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, in partnership with the Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Johann PelletMurdoch Children's Research Institute, Melbourne, Australia.
H Rogier van DoornOxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, in partnership with the Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Anh Tuan TranChildren Hospital 1, Ho Chi Minh City, Vietnam.
Bach Hue NguyenChildren Hospital 1, Ho Chi Minh City, Vietnam.
Thi Thu Loan TranChildren Hospital 2, Ho Chi Minh City, Vietnam.
Quynh Huong TranChildren Hospital 2, Ho Chi Minh City, Vietnam.
Quoc Bao VoChildren Hospital 2, Ho Chi Minh City, Vietnam.
Nguyen Anh Tran DacChildren Hospital 2, Ho Chi Minh City, Vietnam.
Hong Nhien TrinhChildren Hospital 1, Ho Chi Minh City, Vietnam.
Thi Thanh Hai NguyenChildren Hospital 1, Ho Chi Minh City, Vietnam.
Bao Tinh Le BinhChildren Hospital 1, Ho Chi Minh City, Vietnam.
Huu Mai Khanh NguyenChildren Hospital 1, Ho Chi Minh City, Vietnam.
Minh Tien NguyenChildren Hospital 1, Ho Chi Minh City, Vietnam.
Quang Tung ThaiChildren Hospital 1, Ho Chi Minh City, Vietnam.
Thanh Vu VoChildren Hospital 1, Ho Chi Minh City, Vietnam.
Ngoc Quang Minh NgoChildren Hospital 1, Ho Chi Minh City, Vietnam.
Thi Kim Huyen DangChildren Hospital 2, Ho Chi Minh City, Vietnam.
Ngoc Huong CaoChildren Hospital 2, Ho Chi Minh City, Vietnam.
Thu Van TranChildren Hospital 2, Ho Chi Minh City, Vietnam.
Lu Viet HoChildren Hospital 2, Ho Chi Minh City, Vietnam.
Bertrand De MeulderEuropean Institute for Systems Biology and Medicine, Lyon, France.
Charles AuffrayEuropean Institute for Systems Biology and Medicine, Lyon, France.
Jorrit-Jan HofstraDepartment of Medical Microbiology, Academic Medical Center, University of Amsterdam, The Netherlands.
Jeremy FarrarOxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, in partnership with the Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Juliet E BryantOxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, in partnership with the Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Menno de JongOxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, in partnership with the Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Martin L HibberdGenome Institute of Singapore.
Children's Hospital 2 · VNHospital for Tropical Diseases · VNEuropean Institute for Systems Biology and MedicineGenome Institute of Singapore · SGMurdoch Children's Research Institute · AUOxford University Clinical Research Unit · VNUniversity of Amsterdam · NL

Funding

Wellcome TrustWellcome Trust 077078/Z/05/Z
6 · The paper itself

Abstract

Background: Most insights into the cascade of immune events after acute respiratory syncytial virus (RSV) infection have been obtained from animal experiments or in vitro models. Methods: In this study, we investigated host gene expression profiles in nasopharyngeal (NP) swabs and whole blood samples during natural RSV and rhinovirus (hRV) infection (acute versus early recovery phase) in 83 hospitalized patients <2 years old with lower respiratory tract infections. Results: Respiratory syncytial virus infection induced strong and persistent innate immune responses including interferon signaling and pathways related to chemokine/cytokine signaling in both compartments. Interferon-α/β, NOTCH1 signaling pathways and potential biomarkers HIST1H4E, IL7R, ISG15 in NP samples, or BCL6, HIST2H2AC, CCNA1 in blood are leading pathways and hub genes that were associated with both RSV load and severity. The observed RSV-induced gene expression patterns did not differ significantly in NP swab and blood specimens. In contrast, hRV infection did not as strongly induce expression of innate immunity pathways, and significant differences were observed between NP swab and blood specimens. Conclusions: We conclude that RSV induced strong and persistent innate immune responses and that RSV severity may be related to development of T follicular helper cells and antiviral inflammatory sequelae derived from high activation of BCL6.

Indexed as

Gene Expression ProfilingImmunity, InnateBlood CellsChild, PreschoolCohort StudiesCommon ColdFemaleHospitalizationHumansInfantInfant, NewbornMaleRespiratory MucosaRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsRespiratory Tract Infectionschildren under 2 years oldhost expression profilelower respiratory tract infectionsrespiratory syncytial virusrhinovirus

Identifiers

PMID29029245
PMCPMC5853303
OpenAlexW2758001830

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.