Evidence map›Paper›PMID 24785236›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2014

Differential impact of respiratory syncytial virus and parainfluenza virus on the frequency of acute otitis media is explained by lower adaptive and innate immune responses in otitis-prone children.

David Verhoeven, Qingfu Xu, Michael E Pichichero

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Prevention of antimicrobial prescribing among infants following maternal vaccination against respiratory syncytial virus.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  9. Respiratory Syncytial Virus's Non-structural Proteins: Masters of Interference.Frontiers in cellular and infection microbiology · 2020
    Review
  10. Impaired Proinflammatory Response in Stringently Defined Otitis-prone Children During Viral Upper Respiratory Infections.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Importance of viruses in acute otitis media.Current opinion in pediatrics · 2015
    Review
  16. 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

3 authors at 1 institution in 1 country.

David VerhoevenRochester General Hospital Research Institute, Rochester General Hospital, New York.
Qingfu XuRochester General Hospital Research Institute, Rochester General Hospital, New York.
Michael E PichicheroRochester General Hospital Research Institute, Rochester General Hospital, New York.
Rochester General Hospital · US

Funding

NTHi Immunity in Young ChildrenR01DC008671 · NIDCD · UNIVERSITY OF ROCHESTER · PI PICHICHERO, MICHAEL E · 2007 to 2016
$5.8M
Analysis of Pro-inflammatory Memory CD4 T-cell Subsets to Influenza InfectionK22AI089975 · NIAID · ROCHESTER GENERAL HOSPITAL (NY) · PI VERHOEVEN, DAVID E · 2010 to 2011
$270k
NIAID NIH HHS K22 AI089975NIAID NIH HHS K22AI089975NIDCD NIH HHS R01 DC008671NIDCD NIH HHS R01DC008671
6 · The paper itself

Abstract

backgroundAcute otitis media (AOM) is a leading cause of bacterial pediatric infections associated with viral upper respiratory infections (URIs). We examined the differential impact of respiratory syncytial virus (RSV) and parainfluenza virus URIs on the frequency of AOM caused by Streptococcus pneumoniae (Spn) and nontypeable Haemophilus influenzae (NTHi) in stringently defined otitis-prone (sOP) and non-otitis-prone (NOP) children as a potential mechanism to explain increased susceptibility to AOM.

methodsPeripheral blood and nasal washes were obtained from sOP and NOP children (n = 309). Colonization events and antiviral responses consisting of total specific immunoglobulin G (IgG) responses, neutralizing antibody responses, and T-cell responses were determined. Isolated neutrophils were infected with varying multiplicities of infection of both viruses, and opsonophagocytosis potential was measured.

resultsA significant increase was found in frequency of AOM events caused by Spn and NTHi, with a concurrent RSV infection in sOP children. These results correlated with diminished total RSV-specific IgG, higher viral nasal burdens, and lower IgG neutralizing capacity. The sOP children had diminished T-cell responses to RSV that correlated with lower Toll-like receptor 3/7 transcript and decreased expression of HLA-DR on antigen-presenting cells. RSV interfered with the Spn phagocytic capacity of neutrophils in a dose-dependent manner. Parainfluenza virus infections did not differentially affect AOM events in sOP and NOP children.

conclusionsLower innate and adaptive immune responses to RSV in sOP children may slow the kinetics of viral clearance from the nasopharynx and allow for viral interference with antibacterial immune responses, thus contributing to increased frequency of AOMs.

Indexed as

Adaptive ImmunityImmunity, InnateAcute DiseaseChild, PreschoolFemaleHaemophilus influenzaeHLA-DR AntigensHumansInfantMaleNasopharynxOtitis MediaParamyxoviridaeProspective StudiesRespiratory Syncytial VirusesStreptococcus pneumoniaeHLA-DR AntigensTLR3 protein, humanTLR7 protein, humanToll-Like Receptor 3Toll-Like Receptor 7acute otitis mediaadaptive immune responsesotitis-prone childrenparainfluenza virusrespiratory syncytial virus

Identifiers

PMID24785236
PMCPMC4155442
OpenAlexW2131787276

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.