Evidence map›Paper›PMID 30875826›Full record

ArticleInternational journal of molecular sciences2019

Interleukin-1 Receptor Antagonist Modulates Liver Inflammation and Fibrosis in Mice in a Model-Dependent Manner.

Raphael P H Meier, Jeremy Meyer, Elisa Montanari, Stephanie Lacotte, Alexandre Balaphas, Yannick D Muller, Sophie Clément, Francesco Negro, Christian Toso, Philippe Morel and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. COX2Physiological reports · 2026
    Article
  4. Review
  5. Review
  6. IL-1 family of cytokines in gastrointestinal and liver disorders.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. IL-1 receptor antagonist: etiological and drug delivery systems overview.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  12. Article
  13. Review
  14. Review
  15. Therapeutic Perspectives of IL1 Family Members in Liver Diseases: An Update.Journal of clinical and translational hepatology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. 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

11 authors at 2 institutions in 2 countries.

Raphael P H MeierVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Raphael.Meier@hcuge.ch.ORCID 0000-0001-9050-0436
Jeremy MeyerVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Jeremy.Meyer@hcuge.ch.
Elisa MontanariVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Elisa.Montanari@unige.ch.
Stephanie LacotteVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Stephanie.Lacotte@unige.ch.ORCID 0000-0002-5921-6389
Alexandre BalaphasVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Alexandre.Balaphas@hcuge.ch.ORCID 0000-0001-9039-6579
Yannick D MullerTransplant Surgery, University of California San Francisco, San Francisco, CA 94143, USA. Yannick.Muller@ucsf.edu.
Sophie ClémentDivision of Clinical Pathology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Sophie.Clement@unige.ch.
Francesco NegroDivision of Clinical Pathology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Francesco.Negro@hcuge.ch.
Christian TosoVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Christian.Toso@hcuge.ch.
Philippe MorelVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Philippe.Morel@hcuge.ch.
Leo H BuhlerVisceral and Transplant Surgery, Department of Surgery, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland. Leo.Buhler@hcuge.ch.
University Hospital of Geneva · CHUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-1 (IL-1)β and IL-1 receptor antagonist (IL-1Ra) have been proposed as important mediators during chronic liver diseases. We aimed to determine whether the modulation of IL-1β signaling with IL-1Ra impacts on liver fibrosis.

methodsWe assessed the effects of IL-1β on human hepatic stellate cells (HSC) and in mouse models of liver fibrosis induced by bile duct ligation (BDL) or carbon tetrachloride treatment (CCl-4).

resultsHuman HSCs treated with IL-1β had increased IL-1β, IL-1Ra, and MMP-9 expressions in vitro. HSCs treated with IL-1β had reduced α-smooth muscle actin expression. These effects were all prevented by IL-1Ra treatment. In the BDL model, liver fibrosis and Kuppfer cell numbers were increased in IL-1Ra KO mice compared to wild type mice and wild type mice treated with IL-1Ra. In contrast, after CCl-4 treatment, fibrosis, HSC and Kupffer cell numbers were decreased in IL-1Ra KO mice compared to the other groups. IL-1Ra treatment provided a modest protective effect in the BDL model and was pro-fibrotic in the CCl-4 model.

conclusionsWe demonstrated bivalent effects of IL-1Ra during liver fibrosis in mice. IL-1Ra was detrimental in the CCl-4 model, whereas it was protective in the BDL model. Altogether these data suggest that blocking IL-1-mediated inflammation may be beneficial only in selective liver fibrotic disease.

Indexed as

ActinsAnimalsCarbon TetrachlorideCell CountCells, CulturedDisease Models, AnimalGene Expression RegulationGene Knockout TechniquesHumansInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinKupffer CellsLiver CirrhosisMaleMatrix Metalloproteinase 9MiceACTA2 protein, humanActinsCarbon TetrachlorideIL1B protein, humanIL1RN protein, humanInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinMatrix Metalloproteinase 9MMP9 protein, humanbile duct ligationcarbon tetracholorideinsulininterleukin-1interleukin-1 receptor antagonistliver fibrosis

Identifiers

PMID30875826
PMCPMC6471711
OpenAlexW2921992014

What OpenQuestion holds

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LicenceCC BY
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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.