Evidence map›Paper›PMID 31001253›Full record

ArticleFrontiers in immunology2019

Comparison of Mesenchymal Stromal Cells From Different Origins for the Treatment of Graft-vs.-Host-Disease in a Humanized Mouse Model.

Céline Grégoire, Caroline Ritacco, Muriel Hannon, Laurence Seidel, Loïc Delens, Ludovic Belle, Sophie Dubois, Sophie Vériter, Chantal Lechanteur, Alexandra Briquet and 4 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
7.7field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

  1. Pooled it
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  7. [Research advances in mesenchymal stem cell therapy for graft-versus-host disease].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2026
    Review
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  9. Article
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  17. Mesenchymal stromal cell therapy: Progress to date and future outlook.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  18. Article
  19. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  20. Article
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

14 authors at 2 institutions in 1 country.

Céline GrégoireHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Caroline RitaccoHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Muriel HannonHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Laurence SeidelDepartment of Biostatistics, SIMÉ, University Hospital Center of Liège, Liège, Belgium.
Loïc DelensHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Ludovic BelleHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Sophie DuboisHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Sophie VériterEndocrine Cell Therapy, Centre of Tissue and Cellular Therapy, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Chantal LechanteurLaboratory of Cell and Gene Therapy, University Hospital Center and University of Liège, Liège, Belgium.
Alexandra BriquetLaboratory of Cell and Gene Therapy, University Hospital Center and University of Liège, Liège, Belgium.
Sophie ServaisHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Gregory EhxHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Yves BeguinHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
Frédéric BaronHematology Research Unit, GIGA-I3, GIGA Institute, University of Liège, Liège, Belgium.
University of Liège · BECliniques Universitaires Saint-Luc · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) have potent immunomodulatory properties that make them an attractive tool against graft- vs.-host disease (GVHD). However, despite promising results in phase I/II studies, bone marrow (BM-) derived MSCs failed to demonstrate their superiority over placebo in the sole phase III trial reported thus far. MSCs from different tissue origins display different characteristics, but their therapeutic benefits have never been directly compared in GVHD. Here, we compared the impact of BM-, umbilical cord (UC-), and adipose-tissue (AT-) derived MSCs on T-cell function

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsDisease Models, AnimalGraft vs Host DiseaseHumansMesenchymal Stem CellsMiceOrgan SpecificityTh17 CellsT-Lymphocytes, Regulatoryadipose tissuebone marrowgraft-vs.-host-diseasehematopoietic stem cell transplantationmesenchymal stromal cellsNSGumbilical cordxenogeneic

Identifiers

PMID31001253
PMCPMC6454068
OpenAlexW2926032340

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.