Evidence map›Paper›PMID 28926619›Full record

ArticlePloS one2017

Liver X receptor activation promotes differentiation of regulatory T cells.

Martin Herold, Johanna Breuer, Stephanie Hucke, Percy Knolle, Nicholas Schwab, Heinz Wiendl, Luisa Klotz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  11. Cholesterol metabolism: a new molecular switch to control inflammation.Clinical science (London, England : 1979) · 2021
    Review
  12. LXR directly regulates glycosphingolipid synthesis and affects human CD4+ T cell function.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. T-cell regulation of fibroblasts and cardiac fibrosis.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Review
  19. Metabolic signaling in T cells.Cell research · 2020
    Review
  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

7 authors.

Martin HeroldDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.ORCID http://orcid.org/0000-0002-3147-1281
Johanna BreuerDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.
Stephanie HuckeDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.
Percy KnolleInstitute of Molecular Immunology & Experimental Oncology, Technical University Munich, Munich, Germany.
Nicholas SchwabDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.
Heinz WiendlDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.
Luisa KlotzDepartment of Neurology, University of Muenster, Albert-Schweitzer-Campus 1, Muenster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nuclear receptor Liver X Receptor (LXR) is a ligand-activated transcription factor that has been implicated in control of chronic inflammation by downregulating pro-inflammatory T cell responses. An impaired function of regulatory T cells, a subset of CD4+ T cells with a crucial role in maintaining lymphocytes homeostasis and immune regulation, is frequently observed in chronic inflammatory diseases. We observed that pharmacological activation of LXR in T cells not only resulted in a thorough suppression of Th1 and Th17 polarization in vitro, but also significantly induced regulatory T cells (Treg) cell differentiation in a receptor-specific fashion. In line with this, systemic LXR activation by oral treatment of mice with the LXR agonist GW3965 induced gut-associated regulatory T cells in vivo. Importantly, such LXR-activated Tregs had a higher suppressive capacity in functional in vitro coculture assays with effector T cells. Our data thus point towards a dual role of LXR-mediated control of inflammation by suppression of pro-inflammatory T cells and reciprocal induction of regulatory T cells.

Indexed as

Administration, OralAnimalsBenzoatesBenzylaminesCD4-Positive T-LymphocytesCell DifferentiationCoculture TechniquesCytokinesEnzyme-Linked Immunosorbent AssayIntestinal MucosaIntestinesLiver X ReceptorsLymph NodesMiceMice, KnockoutTh17 CellsBenzoatesBenzylaminesCytokinesGW 3965Liver X ReceptorsTransforming Growth Factor beta

Identifiers

PMID28926619
PMCPMC5604992
OpenAlexW2754395007

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.