Evidence map›Paper›PMID 25899567›Full record

ArticleInternational immunology2015

Modulation of dendritic cell alternative activation and function by the vitamin A metabolite retinoic acid.

Lucy H Jones, Peter C Cook, Alasdair C Ivens, Graham D Thomas, Alexander T Phythian-Adams, Judith E Allen, Andrew S MacDonald

Open access · bronzeAbstract read
In one paragraph

Article in International immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. 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

7 authors at 4 institutions in 1 country.

Lucy H JonesInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Scotland, UK.
Peter C CookManchester Collaborative Centre for Inflammation Research, Faculty of Life Sciences, University of Manchester, Manchester M13 9NT, UK.
Alasdair C IvensInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Scotland, UK.
Graham D ThomasInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Scotland, UK.
Alexander T Phythian-AdamsManchester Collaborative Centre for Inflammation Research, Faculty of Life Sciences, University of Manchester, Manchester M13 9NT, UK.
Judith E AllenInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Scotland, UK.
Andrew S MacDonaldManchester Collaborative Centre for Inflammation Research, Faculty of Life Sciences, University of Manchester, Manchester M13 9NT, UK andrew.macdonald@manchester.ac.uk.
University of Edinburgh · GBCentre for Inflammation Research · GBCentre for Immunity, Infection and Evolution · GBUniversity of Manchester · GB

Funding

Medical Research Council G0701437Medical Research Council MR/K01207X/1Wellcome Trust 095831
6 · The paper itself

Abstract

The archetypal Th2 cytokine IL-4 has previously been shown to alternatively activate murine macrophages and, more recently, dendritic cells (DCs) both in vitro and in vivo. IL-4 has also been shown to induce Aldh1a2 (aldehyde dehydrogenase 1a2) expression in murine macrophages recruited to the peritoneal cavity. However, the influence of IL-4 on DC Aldh1a2 induction in vivo has not yet been addressed. In this work, we found that DCs show enhanced aldehyde dehydrogenase enzyme activity in vivo, which led us to investigate the impact of the vitamin A metabolite all-trans retinoic acid (RA) on DC alternative activation and function. Antagonism of RA receptors reduced production of resistin-like molecule alpha by DCs responding to IL-4, while addition of exogenous RA enhanced production of this marker of alternative activation. Functionally, RA increased DC induction of CD4(+) T-cell IL-10, while reducing CD4(+) T-cell IL-4 and IL-13, revealing a previously unidentified role for RA in regulating the ability of alternatively activated DCs to influence Th2 polarization.

Indexed as

Aldehyde DehydrogenaseAnimalsAntigens, SurfaceDendritic CellsEnzyme ActivationFemaleImmunomodulationImmunophenotypingIntercellular Signaling Peptides and ProteinsInterleukin-4MicePhenotypeReceptors, Retinoic AcidSignal TransductionT-LymphocytesTretinoinAldehyde DehydrogenaseAntigens, SurfaceIntercellular Signaling Peptides and ProteinsInterleukin-4Receptors, Retinoic AcidRetnla protein, mouseTretinoinAPCIL-4Th2

Identifiers

PMID25899567
PMCPMC4625886
OpenAlexW2142565008

What OpenQuestion holds

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LicenceCC BY
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.