Evidence map›Paper›PMID 21482736›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Plasmacytoid dendritic cells promote host defense against acute pneumovirus infection via the TLR7-MyD88-dependent signaling pathway.

Sophia Davidson, Gerard Kaiko, Zhixuan Loh, Amit Lalwani, Vivian Zhang, Kirsten Spann, Shen Yun Foo, Nicole Hansbro, Satoshi Uematsu, Shizuo Akira and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. The role of dendritic cells in respiratory viral infection.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  7. Article
  8. Article
  9. CD169eLife · 2022
    Article
  10. Article
  11. Modulation of Vagal Sensory NeuronsFrontiers in physiology · 2021
    Article
  12. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  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

14 authors at 7 institutions in 4 countries.

Sophia DavidsonCentre for Asthma and Respiratory Diseases, University of Newcastle, New South Wales 2300, Australia.
Gerard Kaiko
Zhixuan Loh
Amit Lalwani
Vivian Zhang
Kirsten Spann
Shen Yun Foo
Nicole Hansbro
Satoshi Uematsu
Shizuo Akira
Klaus I Matthaei
Helene F Rosenberg
Paul S Foster
Simon Phipps
University of Queensland · AUHunter Medical Research Institute · AUUniversity of Newcastle Australia · AUAustralian National University · AUNational Institutes of Health · USOsaka International University · JPOsaka University · JP

Funding

Inflammation and Therapy for Respiratory Virus InfectionZIAAI000943 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROSENBERG, HELENE · 2009 to 2020
$7.4M
Intramural NIH HHS Z99 AI999999Intramural NIH HHS ZIA AI000943NIAID NIH HHS Y99 AI999999
6 · The paper itself

Abstract

Human respiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infection in infants. In human infants, plasmacytoid dendritic cells (pDC) are recruited to the nasal compartment during infection and initiate host defense through the secretion of type I IFN, IL-12, and IL-6. However, RSV-infected pDC are refractory to TLR7-mediated activation. In this study, we used the rodent-specific pathogen, pneumonia virus of mice (PVM), to determine the contribution of pDC and TLR7 signaling to the development of the innate inflammatory and early adaptive immune response. In wild-type, but not TLR7- or MyD88-deficient mice, PVM inoculation led to a marked infiltration of pDC and increased expression of type I, II, and III IFNs. The delayed induction of IFNs in the absence of TLR7 or MyD88 was associated with a diminished innate inflammatory response and augmented virus recovery from lung tissue. In the absence of TLR7, PVM-specific CD8(+) T cell cytokine production was abrogated. The adoptive transfer of TLR7-sufficient, but not TLR7-deficient pDC to TLR7 gene-deleted mice recapitulated the antiviral responses observed in wild-type mice and promoted virus clearance. In summary, TLR7-mediated signaling by pDC is required for appropriate innate responses to acute pneumovirus infection. It is conceivable that as-yet-unidentified defects in the TLR7 signaling pathway may be associated with elevated levels of RSV-associated morbidity and mortality among otherwise healthy human infants.

Indexed as

Adaptive ImmunityAdoptive TransferAnimalsDendritic CellsInterferonsMembrane GlycoproteinsMiceMice, Inbred BALB CMice, KnockoutMurine pneumonia virusMyeloid Differentiation Factor 88Pneumovirus InfectionsSignal TransductionToll-Like Receptor 7InterferonsMembrane GlycoproteinsMyd88 protein, mouseMyeloid Differentiation Factor 88Tlr7 protein, mouseToll-Like Receptor 7

Identifiers

PMID21482736
PMCPMC3404606
OpenAlexW2119945903

What OpenQuestion holds

Textmetadata
LicenceTDM
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.