Evidence map›Paper›PMID 39195868›Full record

ArticleNature cardiovascular research2022

Human umbilical cord mesenchymal stem cell-derived treatment of severe pulmonary arterial hypertension.

Georg Hansmann, Philippe Chouvarine, Franziska Diekmann, Martin Giera, Markus Ralser, Michael Mülleder, Constantin von Kaisenberg, Harald Bertram, Ekaterina Legchenko, Ralf Hass

Abstract read
In one paragraph

Article in Nature cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–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.

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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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  7. Review
  8. Genetic and Environmental Contributors To Congenital Heart Disease.Current treatment options in cardiovascular medicine · 2025
    Review
  9. Mesenchymal stem cell therapy for pulmonary hypertension: an update.Frontiers in bioengineering and biotechnology · 2025
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Pulmonary Hypertension: A Contemporary Review.American journal of respiratory and critical care medicine · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. 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

10 authors.

Georg HansmannDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany. georg.hansmann@gmail.com.ORCID http://orcid.org/0000-0003-0709-3935
Philippe ChouvarineDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Franziska DiekmannDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Martin GieraCenter for Proteomics and Metabolomics, Leiden University Medical Center (LUMC), Leiden, Netherlands.
Markus RalserDepartment of Biochemistry, Charité Universitätsmedizin Berlin, Berlin, Germany.
Michael MüllederDepartment of Biochemistry, Charité Universitätsmedizin Berlin, Berlin, Germany.
Constantin von KaisenbergDepartments of Obstetrics, Gynecology and Reproductive Medicine, Hannover Medical School, Hannover, Germany.
Harald BertramDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Ekaterina LegchenkoDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Ralf HassBiochemistry and Tumor Biology Lab, Department of Gynecology, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0000-0002-2481-7547

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) DFG KFO311, grant HA4348/6-2Novo Nordisk Fonden (Novo Nordisk Foundation) NNF21CC0073729
6 · The paper itself

Abstract

Here we report application of human umbilical cord mesenchymal stem cell (HUCMSC)-derived therapy for pulmonary arterial hypertension (PAH). A 3-year-old female presented with heritable PAH associated with hereditary hemorrhagic telangiectasia and was treated for 6 months with serial intravascular infusions of conditioned media (CM) from allogenic HUCMSCs. The treatment markedly improved clinical and hemodynamic parameters and decreased blood plasma markers of vascular fibrosis, injury and inflammation. A comparative analysis of single-cell RNA sequencing data collected from three HUCMSCs and two human umbilical vein endothelial cell (HUVEC) controls identified eight common cell clusters, all of which indicated regenerative potential specific for HUCMSCs. The properties of HUCMSCs were validated by untargeted label-free quantitation of the cell and CM proteome, suggesting increased activity of regeneration, autophagy and anti-inflammation pathways and mitochondrial function. Prostaglandin analysis demonstrated increased HUCMSC secretion of prostaglandin E2, known for its regenerative capacity. Additional prospective clinical studies are warranted to confirm and further explore the benefits of HUCMSC-derived therapy for PAH.

Identifiers

PMID39195868
PMCPMC11358026

What Socratic 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 Socratic graph.