Evidence map›Paper›PMID 24308446›Full record

ArticleAmerican journal of respiratory and critical care medicine2014

Mucosal immune responses predict clinical outcomes during influenza infection independently of age and viral load.

Christine M Oshansky, Andrew J Gartland, Sook-San Wong, Trushar Jeevan, David Wang, Philippa L Roddam, Miguela A Caniza, Tomer Hertz, John P Devincenzo, Richard J Webby and 1 more

Abstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 2 pooled it
10.7field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 2 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Pooled it
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  12. Multivariate Host-Pathogen Interactions Driving Heterogeneous Viral Shedding and CD8medRxiv : the preprint server for health sciences · 2025
    Article
  13. Article
  14. Article
  15. ZBP1-driven cell death in severe influenza.Trends in microbiology · 2025
    Review
  16. Deep insight into cytokine storm: from pathogenesis to treatment.Signal transduction and targeted therapy · 2025
    Review
  17. Article
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  19. Review
  20. Article

70 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Christine M Oshansky1 Department of Immunology, and.
Andrew J Gartland
Sook-San Wong
Trushar Jeevan
David Wang
Philippa L Roddam
Miguela A Caniza
Tomer Hertz
John P Devincenzo
Richard J Webby
Paul G Thomas
St. Jude Children's Research Hospital · USFred Hutch Cancer Center · USUniversity of Tennessee Health Science Center · USInstitute of Immunology · HR

Funding

NIAID NIH HHS HHSN266200700005CPHS HHS HSN266200700005C
6 · The paper itself

Abstract

rationaleChildren are an at-risk population for developing complications following influenza infection, but immunologic correlates of disease severity are not understood. We hypothesized that innate cellular immune responses at the site of infection would correlate with disease outcome.

objectivesTo test the immunologic basis of severe illness during natural influenza virus infection of children and adults at the site of infection.

methodsAn observational cohort study with longitudinal sampling of peripheral and mucosal sites in 84 naturally influenza-infected individuals, including infants. Cellular responses, viral loads, and cytokines were quantified from nasal lavages and blood, and correlated to clinical severity. MEASUREMENTS AND MAIN

resultsWe show for the first time that although viral loads in children and adults were similar, innate responses in the airways were stronger in children and varied considerably between plasma and site of infection. Adjusting for age and viral load, an innate immune profile characterized by increased nasal lavage monocyte chemotactic protein-3, IFN-α2, and plasma IL-10 levels at enrollment predicted progression to severe disease. Increased plasma IL-10, monocyte chemotactic protein-3, and IL-6 levels predicted hospitalization. This inflammatory cytokine production correlated significantly with monocyte localization from the blood to the site of infection, with conventional monocytes positively correlating with inflammation. Increased frequencies of CD14(lo) monocytes were in the airways of participants with lower inflammatory cytokine levels.

conclusionsAn innate profile was identified that correlated with disease progression independent of viral dynamics and age. The airways and blood displayed dramatically different immune profiles emphasizing the importance of cellular migration and localized immune phenotypes.

Indexed as

Immunity, InnateSeverity of Illness IndexAdolescentAdultAge FactorsBiomarkersChemotaxis, LeukocyteChildChild, PreschoolCohort StudiesCytokinesFemaleFlow CytometryHospitalizationHumansInfantBiomarkersCytokines

Identifiers

PMID24308446
PMCPMC3977720
OpenAlexW2120977330

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.