Evidence map›Paper›PMID 37701336›Full record

ArticleJHEP reports : innovation in hepatology2023

Therapeutic targeting of adipose tissue macrophages ameliorates liver fibrosis in non-alcoholic fatty liver disease.

Celia Martínez-Sánchez, Octavi Bassegoda, Hongping Deng, Xènia Almodóvar, Ainitze Ibarzabal, Ana de Hollanda, Raquel-Adela Martínez García de la Torre, Delia Blaya, Silvia Ariño, Natalia Jiménez-Esquivel and 24 more

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Macrophage Plg-RJournal of thrombosis and haemostasis : JTH · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. 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

34 authors at 6 institutions in 3 countries.

Celia Martínez-SánchezFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Octavi BassegodaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Hongping DengMicro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Xènia AlmodóvarFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Ainitze IbarzabalFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Ana de HollandaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Raquel-Adela Martínez García de la TorreFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Delia BlayaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Silvia AriñoFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Natalia Jiménez-EsquivelLiver Unit, Hospital Clínic of Barcelona, Faculty of Medicine, University of Barcelona, Barcelona, Spain.
Beatriz Aguilar-BravoFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Julia VallverdúCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
Carla MontironiMolecular Biology Core & Pathology Department, Hospital Clínic of Barcelona, Spain.
Oscar Osorio-ConlesCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Yiliam FundoraDepartment of General and Digestive Surgery, Hospital Clinic de Barcelona, Barcelona, Spain.
Francisco Javier Sánchez MorenoDepartment of General and Digestive Surgery, Hospital Clinic de Barcelona, Barcelona, Spain.
Alicia G Gómez-ValadésNeuronal Control of Metabolism (NeuCoMe) Laboratory, Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Laia Aguilar-CorominasFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Anna SoriaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Elisa PoseFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Adrià JuanolaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Marta CerveraFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Martina PerezFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Virginia Hernández-GeaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Silvia AffòFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Kelly S SwansonDivision of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Joana Ferrer-FàbregaCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
Jose Maria BalibreaEndocrine, Metabolic & Bariatric Surgery Unit, Germans Trias i Pujol Hospital, Autonomous University of Barcelona, Barcelona, Spain.
Pau Sancho-BruFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Josep VidalFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Pere GinèsFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Andrew M SmithMicro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Isabel GrauperaFundació de Recerca Clínic Barcelona-Institut d'Investigacións Biomèdiques August Pi i Sunyer (FCRB-IDIABPS), Barcelona, Spain.
Mar CollDepartment of Medicine, University of Barcelona, Barcelona, Spain.
Hospital Clínic de Barcelona · ESFundació Clínic per a la Recerca Biomèdica · ESCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESInstituto de Salud Carlos III · ESUniversity of Illinois Urbana-Champaign · USUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: : The accumulation of adipose tissue macrophages (ATMs) in obesity has been associated with hepatic injury. However, the contribution of ATMs to hepatic fibrosis in non-alcoholic fatty liver disease (NAFLD) remains to be elucidated. Herein, we investigate the relationship between ATMs and liver fibrosis in patients with patients with NAFLD and evaluate the impact of modulation of ATMs over hepatic fibrosis in an experimental non-alcoholic steatohepatitis (NASH) model. Methods: Adipose tissue and liver biopsies from 42 patients with NAFLD with different fibrosis stages were collected. ATMs were characterised by immunohistochemistry and flow cytometry and the correlation between ATMs and liver fibrosis stages was assessed. Selective modulation of the ATM phenotype was achieved by Results: Patients with NAFLD presented an increased accumulation of pro-inflammatory ATMs that correlated with hepatic fibrosis. Long-term modulation of ATMs significantly reduced pro-inflammatory phenotype and ameliorated adipose tissue inflammation. Moreover, ATMs modulation was associated with an improvement in steatosis and hepatic inflammation and significantly reduced fibrosis progression in an experimental NASH model. Conclusions: Pro-inflammatory ATMs increase in parallel with fibrosis degree in patients with NAFLD and their modulation in an experimental NASH model improves liver fibrosis, uncovering the potential of ATMs as a therapeutic target to mitigate liver fibrosis in NAFLD. Impact and implications: We report that human adipose tissue pro-inflammatory macrophages correlate with hepatic fibrosis in non-alcoholic fatty liver disease (NAFLD). Furthermore, the modulation of adipose tissue macrophages (ATMs) by dextran-nanocarrier conjugated with dexamethasone shifts the pro-inflammatory phenotype of ATMs to an anti-inflammatory phenotype in an experimental murine model of non-alcoholic steatohepatitis. This shift ameliorates adipose tissue inflammation, hepatic inflammation, and fibrosis. Our results highlight the relevance of adipose tissue in NAFLD pathophysiology and unveil ATMs as a potential target for NAFLD.

Indexed as

Adipose tissue inflammationDextran dexamethasone conjugatesDrug deliveryLiver injuryNanomedicineNanoparticleNon-alcoholic steatohepatitisTargeted therapy

Identifiers

PMID37701336
PMCPMC10494470
OpenAlexW4382458834

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.