Evidence map›Paper›PMID 31591593›Full record

ArticleNature medicine2019

Safety profile of autologous macrophage therapy for liver cirrhosis.

Francesca Moroni, Benjamin J Dwyer, Catriona Graham, Chloe Pass, Laura Bailey, Lisa Ritchie, Donna Mitchell, Alison Glover, Audrey Laurie, Stuart Doig and 13 more

Registry-linked trialAbstract readClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in Nature medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06823713 (An Open-label Phase 1/2 Multicentre Study to Evaluate the Safety, Tolerability and Efficacy of RTX001 Autologous Macrophages in Participants With Liver Cirrhosis Who Have Hepatic Decompensation), which is not on this map. Cited by 115 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT06823713 phase1 / phase2active not recruitingnot on this mapstarted 2024, after this paper: background citation

An Open-label Phase 1/2 Multicentre Study to Evaluate the Safety, Tolerability and Efficacy of RTX001 Autologous Macrophages in Participants With Liver Cirrhosis Who Have Hepatic Decompensation (EMERALD)

TypeinterventionalSponsorResolution Therapeutics LimitedRan2024 to 2028Enrolled30ConditionsEnd-stage Liver Disease (ESLD), Cirrhosis, Liver, Cirrhosis, Decompensated, Liver DiseasesArmsRTX001
3 · Its place in the literature

Who cites it

115 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Bone Marrow-Derived Stem Cells for Patients with Liver Cirrhosis: A Systematic Review and Meta-analysis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2021
    Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Reprogramming macrophages to treat liver diseases.Hepatology (Baltimore, Md.) · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Targeting macrophages in liver fibrosis.Frontiers in immunology · 2026
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article

55 more citing papers are in PubMed but not listed here.

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

23 authors.

Francesca MoroniMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Benjamin J DwyerMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Catriona GrahamEdinburgh Clinical Research Facility, University of Edinburgh, Edinburgh, UK.
Chloe PassTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Laura BaileyTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Lisa RitchieTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Donna MitchellTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Alison GloverTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Audrey LaurieTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Stuart DoigTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Emily HargreavesTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Alasdair R FraserTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.ORCID http://orcid.org/0000-0001-7822-650X
Marc L TurnerTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
John D M CampbellTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Neil W A McGowanTissues, Cells and Advanced Therapeutics, Scottish National Blood Transfusion Service (SNBTS), Edinburgh, UK.
Jacqueline BarryCell and Gene Therapy Catapult, 12th Floor Tower Wing, Guy's Hospital, Great Maze Pond, London, UK.
Joanna K MooreMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Peter C HayesCentre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Diana J LeemingNordic Bioscience, Fibrosis Biology and Biomarkers, Herlev, Denmark.
Mette J NielsenNordic Bioscience, Fibrosis Biology and Biomarkers, Herlev, Denmark.
Kishwar MusaNordic Bioscience, Fibrosis Biology and Biomarkers, Herlev, Denmark.
Jonathan A FallowfieldCentre for Inflammation Research, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-5741-1471
Stuart J ForbesMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK. stuart.forbes@ed.ac.uk.ORCID http://orcid.org/0000-0003-3715-2561

Funding

Medical Research Council G84/6205Medical Research Council MC_PC_16043Medical Research Council MR/K017047/1Medical Research Council MR/M007588/1Medical Research Council MR/R015635/1
6 · The paper itself

Abstract

Therapies to reduce liver fibrosis and stimulate organ regeneration are urgently needed. We conducted a first-in-human, phase 1 dose-escalation trial of autologous macrophage therapy in nine adults with cirrhosis and a Model for End-Stage Liver Disease (MELD) score of 10-16 (ISRCTN 10368050). Groups of three participants received a single peripheral infusion of 10

Indexed as

AgedCell- and Tissue-Based TherapyDose-Response Relationship, ImmunologicEnd Stage Liver DiseaseFemaleHumansLiverLiver CirrhosisLiver RegenerationMacrophagesMaleMiddle Aged

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.