Evidence map›Paper›PMID 25760420›Full record

ArticleMucosal immunology2015

MyD88 dependence of beryllium-induced dendritic cell trafficking and CD4⁺ T-cell priming.

A S McKee, D G Mack, F Crawford, A P Fontenot

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. A comprehensive summary of disease variants implicated in metal allergy.Journal of toxicology and environmental health. Part B, Critical reviews · 2022
    Review
  4. Innate and Adaptive Immunity in Noninfectious Granulomatous Lung Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Immunologic Effects of Beryllium Exposure.Annals of the American Thoracic Society · 2018
    Review
  16. Old and new adjuvants.Current opinion in immunology · 2017
    Review
  17. Review
  18. 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

4 authors at 2 institutions in 1 country.

A S McKeeDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
D G MackDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
F CrawfordDepartment of Immunology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
A P FontenotDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
University of Colorado Anschutz Medical Campus · USNational Jewish Health · US

Funding

T Cells in Beryllium Sensitization and DiseaseP01ES011810 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI NEWMAN, LEE S · 2002 to 2013
$14.0M
PATHOGENIC T CELLS IN CHRONIC BERYLLIUM DISEASER01HL062410 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI FONTENOT, ANDREW P. · 1998 to 2017
$5.7M
Innate effects of beryllium on pulmonarydendritic cell function in chronic beryllium diseaseR01HL126736 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKEE, AMY STRAW · 2016 to 2020
$1.9M
Development of an HLA-DP2 Transgenic Murine Model of Chronic Beryllium DiseaseR21HL111760 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI FONTENOT, ANDREW P. · 2012 to 2013
$387k
NHLBI NIH HHS HL111760NHLBI NIH HHS R01 HL062410NHLBI NIH HHS R01 HL126736NHLBI NIH HHS R21 HL111760NIEHS NIH HHS ES11810NIEHS NIH HHS P01 ES011810
6 · The paper itself

Abstract

Beryllium exposure results in beryllium hypersensitivity in a subset of exposed individuals, leading to granulomatous inflammation and fibrosis in the lung. In addition to its antigenic properties, beryllium has potent adjuvant activity that contributes to sensitization via unknown pathways. Here we show that beryllium induces cellular death and release of interleukin (IL)-1α and DNA into the lung. Release of IL-1α was inflammasome independent and required for beryllium-induced neutrophil recruitment into the lung. Beryllium enhanced classical dendritic cell (cDC) migration from the lung to draining lymph nodes (LNs) in an IL-1R-independent manner, and the accumulation of activated cDCs in the LN was associated with increased priming of CD4(+) T cells. DC migration was reduced in Toll-like receptor 9 knockout (TLR9KO) mice; however, cDCs in the LNs of TLR9-deficient mice were highly activated, suggesting a role for more than one innate receptor in the effects on DCs. The adjuvant effects of beryllium on CD4(+) T-cell priming were similar in wild-type, IL-1R-, caspase-1-, TLR2-, TLR4-, TLR7-, and TLR9-deficient mice. In contrast, DC migration, activation, and the adjuvant effects of beryllium were significantly reduced in myeloid differentiation primary response gene 88 knockout (MyD88KO) mice. Collectively, these data suggest that beryllium exposure results in the release of damage-associated molecular patterns that engage MyD88-dependent receptors to enhance pulmonary DC function.

Indexed as

AnimalsBerylliosisBerylliumCD4-Positive T-LymphocytesCell MovementDendritic CellsDisease Models, AnimalFlow CytometryHumansLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMyeloid Differentiation Factor 88NeutrophilsBerylliumMyd88 protein, mouseMyeloid Differentiation Factor 88

Identifiers

PMID25760420
PMCPMC4567547
OpenAlexW1996694053

What OpenQuestion holds

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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.