Evidence map›Paper›PMID 29045741›Full record

Observational studyThe Journal of infectious diseases2017

Respiratory Syncytial Virus Genotypes, Host Immune Profiles, and Disease Severity in Young Children Hospitalized With Bronchiolitis.

Rosa Rodriguez-Fernandez, Lorena I Tapia, Chin-Fen Yang, Juan Pablo Torres, Susana Chavez-Bueno, Carla Garcia, Lisa M Jaramillo, Melissa Moore-Clingenpeel, Hasan S Jafri, Mark E Peeples and 3 more

Abstract readObservational Study
In one paragraph

Observational study 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 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–field-weighted citation impact
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

53 citing papers in PubMed.

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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

13 authors.

Rosa Rodriguez-FernandezCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Lorena I TapiaDepartment of Molecular Virology and Microbiology, and Pediatrics, Baylor College of Medicine, Houston, Texas.
Chin-Fen YangDepartment of Research, Medimmune LLC, Mountain View, California.
Juan Pablo TorresDivision of Pediatric Infectious Diseases, University of Texas Southwestern Medical Center, Dallas.
Susana Chavez-BuenoDivision of Pediatric Infectious Diseases, University of Texas Southwestern Medical Center, Dallas.
Carla GarciaDivision of Pediatric Infectious Diseases, University of Texas Southwestern Medical Center, Dallas.
Lisa M JaramilloCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Melissa Moore-ClingenpeelCenter for Biostatistics.
Hasan S JafriDivision of Pediatric Infectious Diseases, University of Texas Southwestern Medical Center, Dallas.
Mark E PeeplesCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Pedro A PiedraDepartment of Molecular Virology and Microbiology, and Pediatrics, Baylor College of Medicine, Houston, Texas.
Octavio RamiloCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Asuncion MejiasCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.

Funding

Project 3: Dr. LiP01AI112524 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI LI, JIANRONG · 2015 to 2019
$6.8M
NIAID NIH HHS P01 AI112524
6 · The paper itself

Abstract

Background: Data on how respiratory syncytial virus (RSV) genotypes influence disease severity and host immune responses is limited. Here, we characterized the genetic variability of RSV during 5 seasons, and evaluated the role of RSV subtypes, genotypes, and viral loads in disease severity and host transcriptional profiles. Methods: A prospective, observational study was carried out, including a convenience sample of healthy infants hospitalized with RSV bronchiolitis. Nasopharyngeal samples for viral load quantitation, typing, and genotyping, and blood samples for transcriptome analyses were obtained within 24 hours of hospitalization. Multivariate models were constructed to identify virologic and clinical variables predictive of clinical outcomes. Results: We enrolled 253 infants (median age 2.1 [25%-75% interquartile range] months). RSV A infections predominated over RSV B and showed greater genotype variability. RSV A/GA2, A/GA5, and RSV B/BA were the most common genotypes identified. Compared to GA2 or BA, infants with GA5 infections had higher viral loads. GA5 infections were associated with longer hospital stay, and with less activation of interferon and increased overexpression of neutrophil genes. Conclusions: RSV A infections were more frequent than RSV B, and displayed greater variability. GA5 infections were associated with enhanced disease severity and distinct host immune responses.

Indexed as

GenotypeBronchiolitis, ViralFemaleGene Expression ProfilingGenetic VariationGenotyping TechniquesHospitalizationHumansInfantInterferonsLength of StayMaleNasopharynxNeutrophilsProspective StudiesRespiratory Syncytial Virus, HumanInterferonsbronchiolitisgenomic loadshost responses

Identifiers

PMID29045741
PMCPMC5853407

What OpenQuestion holds

Textmetadata
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.