Evidence map›Paper›PMID 20573305›Full record

ArticleCell transplantation2010

Bone marrow mesenchymal stromal cells attenuate organ injury induced by LPS and burn.

Hiroshi Yagi, Alejandro Soto-Gutierrez, Yuko Kitagawa, Arno W Tilles, Ronald G Tompkins, Martin L Yarmush

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Cell transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06882811 (Clinical Study on Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Sepsis), which is not on this map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% 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.

NCT06882811 early_phase1recruitingnot on this mapstarted 2025, after this paper: background citation

Clinical Study on Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Sepsis

TypeinterventionalSponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical UniversityRan2025 to 2027Enrolled180ConditionsSepsisArmsCD83-positive MSC, regulatory MSC, control solution
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Alternatives to Antibiotics againstAntibiotics (Basel, Switzerland) · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Antibacterial Fusion Protein BPI21/LL-37 Modification Enhances the Therapeutic Efficacy of hUC-MSCs in Sepsis.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  18. Article
  19. Burns in the Elderly: Potential Role of Stem Cells.International journal of molecular sciences · 2020
    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

6 authors at 3 institutions in 2 countries.

Hiroshi YagiDepartment of Surgery, Center for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, MA 02114, USA.
Alejandro Soto-Gutierrez
Yuko Kitagawa
Arno W Tilles
Ronald G Tompkins
Martin L Yarmush
Shriners Hospitals for Children - Erie · USHarvard University · USKeio University · JP

Funding

Engineering of hepatic grafts with decellularized native matricesR00DK083556 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SOTO-GUTIERREZ, ALEJANDRO · 2011 to 2013
$707k
Engineering of hepatic grafts with decellularized native matricesK99DK083556 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SOTO-GUTIERREZ, ALEJANDRO · 2009 to 2010
$180k
NIDDK NIH HHS K99 DK083556NIDDK NIH HHS R00 DK083556
6 · The paper itself

Abstract

Bone marrow mesenchymal stromal cells (MSCs) suppress immune cell responses and have beneficial effects in various inflammatory-related immune disorders. A therapeutic modality for systemic inflammation and its consequences is not available yet. Thus, this work investigates the therapeutic effects of MSCs in injury models induced by lipopolysaccharide (LPS) or burn. Gene expression was analyzed in MSCs when exposed to inflammatory serum from injured animals and it showed remarkable alterations compared to normal culture. In addition, injured animals were transplanted intramuscularly with MSCs. Forty-eight hours after cell transplantation, kidney, lung, and liver were analyzed for infiltration of inflammatory cells and TUNEL-expressing cells. Results showed that MSCs attenuate injury by reducing the infiltration of inflammatory cells in various target organs and by reducing cell death. These data suggest that MSCs emerge as key regulators of immune/inflammatory responses in vivo and as attractive candidates for cell-based treatments for systemic inflammatory-based disorders.

Indexed as

AnimalsBone Marrow CellsBurnsEndotoxemiaGene Expression RegulationHumansInflammationLipopolysaccharidesMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMusclesOrgan SpecificityRatsRats, Sprague-DawleyStromal CellsLipopolysaccharides

Identifiers

PMID20573305
PMCPMC2957544
OpenAlexW2055767345

What OpenQuestion holds

Textmetadata
LicenceTDM
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.