Evidence map›Paper›PMID 19815820›Full record

ArticleCirculation research2009

Progenitor cells from the explanted heart generate immunocompatible myocardium within the transplanted donor heart.

David A D'Alessandro, Jan Kajstura, Toru Hosoda, Alessandro Gatti, Ricardo Bello, Federico Mosna, Silvana Bardelli, Hanqiao Zheng, Domenico D'Amario, M Elena Padin-Iruegas and 9 more

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Circulation research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.4field-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.

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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cardiac allograft vasculopathy: a donor or recipient induced pathology?Journal of cardiovascular translational research · 2015
    Review
  5. Article
  6. Surgical options for the management of ischemic cardiomyopathy.Current treatment options in cardiovascular medicine · 2013
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Stem cell update: highlights from the 2010 Lugano Stem Cell Meeting.Journal of cardiovascular translational research · 2011
    Article
  12. Article
  13. Article
  14. Current and future status of stem cell therapy in heart failure.Current treatment options in cardiovascular medicine · 2010
    Article
  15. Article
  16. Stem cell therapy for heart failure.Methodist DeBakey cardiovascular journal
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

David A D'AlessandroDepartment of Cardiothoracic Surgery, Montefiore Medical Center, Albert Einstein College of Medicine, New York, USA.
Jan Kajstura
Toru Hosoda
Alessandro Gatti
Ricardo Bello
Federico Mosna
Silvana Bardelli
Hanqiao Zheng
Domenico D'Amario
M Elena Padin-Iruegas
Adriana Bastos Carvalho
Marcello Rota
Michael O Zembala
David Stern
Ornella Rimoldi
Konrad Urbanek
Robert E Michler
Annarosa Leri
Piero Anversa
Albert Einstein College of Medicine · USMontefiore Medical Center · US

Funding

Rebuilding the Failing HeartP01HL092868 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO · 2008 to 2013
$12.9M
Stem Cells and Cardiac AgingP01AG023071 · NIA · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2004 to 2008
$9.5M
Repair and Angiogenesis by Stem Cells in Human HeartR37HL081737 · NHLBI · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2005 to 2015
$6.5M
IGF-1, Gender, Heart Failure and Longevity: A Paradigm ShiftR01AG017042 · NIA · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2000 to 2010
$5.3M
Coronary Vasculature Progenitor Cell in Human Ischemic Heart FailureR01HL039902 · NHLBI · NEW YORK UNIVERSITY · PI ANVERSA, PIERO, KAJSTURA, JAN · 1989 to 2012
$4.7M
MYOCYTE STEM CELLS IN THE MAMMALIAN HEARTR01HL065577 · NHLBI · NEW YORK MEDICAL COLLEGE · PI LERI, ANNAROSA · 2000 to 2012
$2.9M
Stem Cells in the Developing HeartR01HL091021 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ROTA, MARCELLO · 2009 to 2013
$2.4M
Redefining Human Myocardial BiologyR01HL105532 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO, BUCHHOLZ, BRUCE A · 2011 to 2014
$2.2M
Cardiac Stem Cell Growth, Aging and DeathR01HL075480 · NHLBI · NEW YORK MEDICAL COLLEGE · PI KAJSTURA, JAN · 2004 to 2008
$1.9M
Cardiac Stem Cells and AngiomyogenesisR01HL111183 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA · 2012 to 2015
$1.7M
Aging and Homeostasis of Cardiac Stem Cell NichesR01AG026107 · NIA · NEW YORK MEDICAL COLLEGE · PI LERI, ANNAROSA · 2006 to 2010
$1.7M
Micro-RNA and Differentitation of Cardiac Progenitor CellsR21HL094894 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI HOSODA, TORU · 2009 to 2010
$816k
NHLBI NIH HHS P01 HL092868NHLBI NIH HHS R01 HL039902NHLBI NIH HHS R01 HL065577NHLBI NIH HHS R01 HL075480NHLBI NIH HHS R01 HL091021NHLBI NIH HHS R01 HL111183NHLBI NIH HHS R21 HL094894NHLBI NIH HHS R37 HL081737NIA NIH HHS P01 AG023071NIA NIH HHS R01 AG017042NIA NIH HHS R01 AG026107
6 · The paper itself

Abstract

rationaleChronic rejection, accelerated coronary atherosclerosis, myocardial infarction, and ischemic heart failure determine the unfavorable evolution of the transplanted heart in humans.

objectiveHere we tested whether the pathological manifestations of the transplanted heart can be corrected partly by a strategy that implements the use of cardiac progenitor cells from the recipient to repopulate the donor heart with immunocompatible cardiomyocytes and coronary vessels. METHODS AND

resultsA large number of cardiomyocytes and coronary vessels were created in a rather short period of time from the delivery, engraftment, and differentiation of cardiac progenitor cells from the recipient. A proportion of newly formed cardiomyocytes acquired adult characteristics and was integrated structurally and functionally within the transplant. Similarly, the regenerated arteries, arterioles, and capillaries were operative and contributed to the oxygenation of the chimeric myocardium. Attenuation in the extent of acute damage by repopulating cardiomyocytes and vessels decreased significantly the magnitude of myocardial scarring preserving partly the integrity of the donor heart.

conclusionsOur data suggest that tissue regeneration by differentiation of recipient cardiac progenitor cells restored a significant portion of the rejected donor myocardium. Ultimately, immunosuppressive therapy may be only partially required improving quality of life and lifespan of patients with cardiac transplantation.

Indexed as

Heart TransplantationHistocompatibilityAnimalsBase SequenceCell DifferentiationCell FusionCoronary VesselsDogsFemaleGenotypeGraft RejectionGreen Fluorescent ProteinsHeart FailureImmunosuppressive AgentsMaleMolecular Sequence DataGreen Fluorescent ProteinsImmunosuppressive Agents

Identifiers

PMID19815820
PMCPMC2801080
OpenAlexW2160099049

What OpenQuestion holds

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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.