Evidence map›Paper›PMID 25950840›Full record

ArticlePloS one2015

Effect of mesenchymal precursor cells on the systemic inflammatory response and endothelial dysfunction in an ovine model of collagen-induced arthritis.

Laura M Dooley, Anwar Abdalmula, Elizabeth A Washington, Claire Kaufman, Elizabeth M Tudor, Peter Ghosh, Silviu Itescu, Wayne G Kimpton, Simon R Bailey

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Mesenchymal STRO-1/STRO-3Future cardiology · 2023
    Review
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  8. Article
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  10. Exercise training improves vascular mitochondrial function.American journal of physiology. Heart and circulatory physiology · 2016
    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

9 authors at 1 institution in 1 country.

Laura M DooleyFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Anwar AbdalmulaFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Elizabeth A WashingtonFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Claire KaufmanFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Elizabeth M TudorFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Peter GhoshMesoblast Ltd, Melbourne, Victoria, Australia.
Silviu ItescuMesoblast Ltd, Melbourne, Victoria, Australia.
Wayne G KimptonFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
Simon R BaileyFaculty of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia.
University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimMesenchymal precursor cells (MPC) are reported to possess immunomodulatory properties that may prove beneficial in autoimmune and other inflammatory conditions. However, their mechanism of action is poorly understood. A collagen-induced arthritis model has been previously developed which demonstrates local joint inflammation and systemic inflammatory changes. These include not only increased levels of inflammatory markers, but also vascular endothelial cell dysfunction, characterised by reduced endothelium-dependent vasodilation. This study aimed to characterise the changes in systemic inflammatory markers and endothelial function following the intravenous administration of MPC, in the ovine model.

methodsArthritis was induced in sixteen adult sheep by administration of bovine type II collagen into the hock joint following initial sensitisation. After 24h, sheep were administered either 150 million allogeneic ovine MPCs intravenously, or saline only. Fibrinogen and serum amyloid-A were measured in plasma to assess systemic inflammation, along with pro-inflammatory and anti-inflammatory cytokines. Animals were necropsied two weeks following arthritis induction. Coronary and digital arterial segments were mounted in a Mulvaney-Halpern wire myograph. The relaxant response to endothelium-dependent and endothelium-independent vasodilators was used to assess endothelial dysfunction. RESULTS AND

conclusionArthritic sheep treated with MPC demonstrated a marked spike in plasma IL-10, 24h following MPC administration. They also showed significantly reduced plasma levels of the inflammatory markers, fibrinogen and serum amyloid A, and increased HDL. Coronary arteries from RA sheep treated with MPCs demonstrated a significantly greater maximal relaxation to bradykinin when compared to untreated RA sheep (253.6 ± 17.1% of pre-contracted tone vs. 182.3 ± 27.3% in controls), and digital arteries also demonstrated greater endothelium-dependent vasodilation. This study demonstrated that MPCs given intravenously are able to attenuate systemic inflammatory changes associated with a monoarthritis, including the development of endothelial dysfunction.

Indexed as

Administration, IntravenousAnimalsArthritis, ExperimentalBradykininCattleCoronary VesselsDisease Models, AnimalEndothelium, VascularFibrinogenInterleukin-10Mesenchymal Stem Cell TransplantationSerum Amyloid A ProteinSheepVasodilator AgentsBradykininFibrinogenInterleukin-10Serum Amyloid A ProteinVasodilator Agents

Identifiers

PMID25950840
PMCPMC4423911
OpenAlexW781671099

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.