Evidence map›Paper›PMID 24043462›Full record

ArticlePurinergic signalling2014

CD39-mediated effect of human bone marrow-derived mesenchymal stem cells on the human Th17 cell function.

Jong Joo Lee, Hyun Jeong Jeong, Mee Kum Kim, Won Ryang Wee, Won Woo Lee, Seung U Kim, Changmin Sung, Yung Hun Yang

Open access · bronzeAbstract read
In one paragraph

Article in Purinergic signalling, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Kinetics of MSC-based enzyme therapy for immunoregulation.Journal of translational medicine · 2019
    Article
  10. Review
  11. Empowering the immune fate of bone marrow mesenchymal stromal cells: gene and protein changes.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Stem Cell Considerations for the Clinician.Physical medicine and rehabilitation clinics of North America · 2016
    Review
  17. Article
  18. The role of purinergic receptors in stem cell differentiation.Computational and structural biotechnology journal · 2015
    Review
  19. Review
  20. 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

8 authors at 6 institutions in 4 countries.

Jong Joo LeeDepartment of Ophthalmology, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Hyun Jeong Jeong
Mee Kum Kim
Won Ryang Wee
Won Woo Lee
Seung U Kim
Changmin Sung
Yung Hun Yang
Seoul National University · KRBiomedical Research Institute · USKonkuk University Medical Center · KRNew Generation University College · ETSeoul National University Hospital · KRUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the immune-modulatory effects of human bone marrow-derived mesenchymal stem cells (hBMSCs) on human Th17 cell function through the CD39-mediated adenosine-producing pathway. The suppressive effects of hBMSCs were evaluated by assessing their effects on the proliferation of Th17 cells and the secretion of interferon (IFN)-γ and interleukin (IL)-17A by Th17 cells with or without anti-CD39 treatment. Changes in CD39 and CD73 expression on the T cells with or without co-culture of hBMSCs were evaluated by flow cytometry. hBMSCs effectively suppressed the proliferation of Th17 cells and the secretion of both IL-17A and IFN-γ from Th17 cells using by both flow cytometry and ELISA, while anti-CD39 treatment significantly reduced the inhibitory effects of hBMSCs on the proliferation and secretion of the Th17 cells. The hBMSCs induced increased expression of the CD39 and CD73 on T cells correlated with the suppressive function of hBMSCs, which was accompanied by increased adenosine production. Our data suggests that hBMSCs can effectively suppress immune responses of the Th17 cells via the CD39-CD73-mediated adenosine-producing pathway.

Indexed as

5'-NucleotidaseAdenosineAntigens, CDApyraseBone Marrow CellsCell ProliferationEnzyme-Linked Immunosorbent AssayFlow CytometryGPI-Linked ProteinsHumansImmune ToleranceMesenchymal Stem CellsOligonucleotide Array Sequence AnalysisSignal TransductionTh17 Cells5'-NucleotidaseAdenosineAntigens, CDApyraseCD39 antigenGPI-Linked ProteinsNT5E protein, human

Identifiers

PMID24043462
PMCPMC4040175
OpenAlexW1977454958

What OpenQuestion holds

Textmetadata
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.