Evidence map›Paper›PMID 22815909›Full record

ArticlePloS one2012

IRF7 regulates TLR2-mediated activation of splenic CD11c(hi) dendritic cells.

Benjamin M J Owens, John W J Moore, Paul M Kaye

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. 25HC regulates the polarization of CD163Frontiers in immunology · 2026
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  14. Modulation of tolerogenic dendritic cells and autoimmunity.Seminars in cell & developmental biology · 2015
    Review
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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 2 institutions in 1 country.

Benjamin M J OwensCentre for Immunology and Infection, Hull York Medical School and Department of Biology, University of York, York, United Kingdom.
John W J Moore
Paul M Kaye
University of York · GBHull York Medical School · GB

Funding

Medical Research Council G0400786Medical Research Council G1000230
6 · The paper itself

Abstract

Members of the Interferon Regulatory Factor (IRF) family of transcription factors play an essential role in the development and function of the immune system. Here we investigated the role of IRF7 in the functional activation of conventional CD11c(hi) splenic dendritic cells (cDCs) in vitro and in vivo. Using mice deficient in IRF7, we found that this transcription factor was dispensable for the in vivo development of cDC subsets in the spleen. However, IRF7-deficient cDCs showed enhanced activation in response to microbial stimuli, characterised by exaggerated expression of CD80, CD86 and MHCII upon TLR2 ligation in vitro. The hyper-responsiveness of Irf7(-/-) cDC to TLR ligation could not be reversed with exogenous IFNα, nor by co-culture with wild-type cDCs, suggesting an intrinsic defect due to IRF7-deficiency. Irf7(-/-) cDCs also had impaired capacity to produce IL-12p70 when stimulated ex vivo, instead producing elevated levels of IL-10 that impaired their capacity to drive Th1 responses. Finally, analysis of bone marrow microchimeric mice revealed that cDCs deficient in IRF7 were also hyper-responsive to TLR2-mediated activation in vivo. Our data suggest a previously unknown function for IRF7 as a component of the regulatory network associated with cDC activation and adds to the wide variety of situations in which these transcription factors play a role.

Indexed as

AnimalsB7-1 AntigenB7-2 AntigenCD11c AntigenCoculture TechniquesDendritic CellsHistocompatibility Antigens Class IIImmune SystemInterferon Regulatory Factor-7MiceMice, Inbred C57BLPhenotypeSpleenToll-Like Receptor 2B7-1 AntigenB7-2 AntigenCD11c AntigenHistocompatibility Antigens Class IIInterferon Regulatory Factor-7TLR2 protein, humanToll-Like Receptor 2

Identifiers

PMID22815909
PMCPMC3398003
OpenAlexW2037783277

What OpenQuestion holds

Textmetadata
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.