Evidence map›Paper›PMID 34341667›Full record

ArticleStem cells international2021

Epicardially Placed Bioengineered Cardiomyocyte Xenograft in Immune-Competent Rat Model of Heart Failure.

Ikeotunye Royal Chinyere, Pierce Bradley, Joshua Uhlorn, Joshua Eason, Saffie Mohran, Giuliana G Repetti, Sherry Daugherty, Jen Watson Koevary, Steven Goldman, Jordan J Lancaster

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.5field-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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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

10 authors at 1 institution in 1 country.

Ikeotunye Royal ChinyereSarver Heart Center, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0002-1674-8270
Pierce BradleySarver Heart Center, University of Arizona, Tucson, AZ, USA.
Joshua UhlornPhysiological Sciences GIDP, University of Arizona, Tucson, AZ, USA.
Joshua EasonSarver Heart Center, University of Arizona, Tucson, AZ, USA.
Saffie MohranDepartment of Biomedical Engineering, University of Arizona, Tucson, AZ, USA.
Giuliana G RepettiSarver Heart Center, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0001-9172-6787
Sherry DaughertySarver Heart Center, University of Arizona, Tucson, AZ, USA.
Jen Watson KoevaryDepartment of Biomedical Engineering, University of Arizona, Tucson, AZ, USA.
Steven GoldmanSarver Heart Center, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0001-7943-1871
Jordan J LancasterSarver Heart Center, University of Arizona, Tucson, AZ, USA.
University of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are under preclinical investigation as a cell-based therapy for heart failure post-myocardial infarction. In a previous study, tissue-engineered cardiac grafts were found to improve hosts' cardiac electrical and mechanical functions. However, the durability of effect, immune response, and

methodshiPSC-CMs and human dermal fibroblasts were cultured into a synthetic bioabsorbable scaffold. The engineered grafts underwent epicardial implantation in infarcted immune-competent male Sprague-Dawley rats. Plasma samples were collected throughout the study to quantify antibody titers. At the study endpoint, all cohorts underwent echocardiographic, hemodynamic, electrophysiologic, and histopathologic assessments.

resultsThe epicardially placed tissue graft therapy improved (

conclusionsThis hiPSC-CM-derived cardiac graft improved systolic and diastolic cardiac function in immune-competent CHF rats. The improvements were detectable at seven weeks post-graft implantation despite an antibody response beginning at week one and peaking at week three. This suggests that non-integrating cell-based therapy delivered by a bioengineered tissue graft for ischemic cardiomyopathy is a viable treatment option.

Identifiers

PMID34341667
PMCPMC8325579
OpenAlexW3184035643

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.