Evidence map›Paper›PMID 28205406›Full record

ArticleStem cells translational medicine2017

Potency of Human Cardiosphere-Derived Cells from Patients with Ischemic Heart Disease Is Associated with Robust Vascular Supportive Ability.

Emma Harvey, Huajun Zhang, Pilar Sepúlveda, Sara P Garcia, Dominic Sweeney, Fizzah A Choudry, Delia Castellano, George N Thomas, Hassan Kattach, Romina Petersen and 5 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

15 authors at 9 institutions in 2 countries.

Emma HarveyRadcliffe Department of Medicine.
Huajun ZhangNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
Pilar SepúlvedaMixed Unit for Cardiovascular Repair, Instituto de Investigación Sanitaria La Fe-Centro de Investigación Príncipe Felipe, Valencia, Spain.
Sara P GarciaDepartment of Haematology.
Dominic SweeneyRadcliffe Department of Medicine.
Fizzah A ChoudryDepartment of Haematology.
Delia CastellanoMixed Unit for Cardiovascular Repair, Instituto de Investigación Sanitaria La Fe-Centro de Investigación Príncipe Felipe, Valencia, Spain.
George N ThomasNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
Hassan KattachNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
Romina PetersenMixed Unit for Cardiovascular Repair, Instituto de Investigación Sanitaria La Fe-Centro de Investigación Príncipe Felipe, Valencia, Spain.
Derek J BlakeMRC Centre for Neuropsychiatric Genetics & Genomics, Cardiff University, Cardiff, United Kingdom.
David P TaggartNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
Mattia FrontiniDepartment of Haematology.
Suzanne M WattRadcliffe Department of Medicine.
Enca Martin-RendonRadcliffe Department of Medicine.
NHS Blood and Transplant · GBCentro de Investigacion Principe Felipe · ESNational Health Service · GBUniversity of Oxford · GBCardiff University · GBInstituto de Investigación Sanitaria La Fe · ESJohn Radcliffe Hospital · GBNuffield Orthopaedic Centre · GBUniversity of Cambridge · GB

Funding

British Heart Foundation RE/13/6/30180Department of Health RP-PG-0310-1003Medical Research Council MR/L010305/1
6 · The paper itself

Abstract

Cardiosphere-derived cell (CDC) infusion into damaged myocardium has shown some reparative effect; this could be improved by better selection of patients and cell subtype. CDCs isolated from patients with ischemic heart disease are able to support vessel formation in vitro but this ability varies between patients. The primary aim of our study was to investigate whether the vascular supportive function of CDCs impacts on their therapeutic potential, with the goal of improving patient stratification. A subgroup of patients produced CDCs which did not efficiently support vessel formation (poor supporter CDCs), had reduced levels of proliferation and increased senescence, despite them being isolated in the same manner and having a similar immunophenotype to CDCs able to support vessel formation. In a rodent model of myocardial infarction, poor supporter CDCs had a limited reparative effect when compared to CDCs which had efficiently supported vessel formation in vitro. This work suggests that not all patients provide cells which are suitable for cell therapy. Assessing the vascular supportive function of cells could be used to stratify which patients will truly benefit from cell therapy and those who would be better suited to an allogeneic transplant or regenerative preconditioning of their cells in a precision medicine fashion. This could reduce costs, culture times and improve clinical outcomes and patient prognosis. Stem Cells Translational Medicine 2017;6:1399-1411.

Indexed as

ApoptosisBlotting, WesternCell MovementCoronary Artery DiseaseFlow CytometryHumansImmunohistochemistryMyocardial IschemiaStem CellsCell-based and tissue-based therapyCoronary artery diseaseHumansMyocardial ischemiaTissue-specific progenitor cells

Identifiers

PMID28205406
PMCPMC5442720
OpenAlexW2591495598

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.