Evidence map›Paper›PMID 23272265›Full record

ArticlePLoS neglected tropical diseases2012

Mesenchymal bone marrow cell therapy in a mouse model of chagas disease. Where do the cells go?

Jasmin, Linda A Jelicks, Wade Koba, Herbert B Tanowitz, Rosalia Mendez-Otero, Antonio C Campos de Carvalho, David C Spray

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.3field-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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Cell-Based Therapies for Heart Failure.Frontiers in pharmacology · 2021
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Unexpected encounter of the parasitic kind.World journal of stem cells · 2019
    Review
  11. Article
  12. Article
  13. The role of nanomaterials in cell delivery systems.Medical molecular morphology · 2018
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Developments in the management of Chagas cardiomyopathy.Expert review of cardiovascular therapy · 2015
    Review
  19. Article
  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

7 authors at 2 institutions in 2 countries.

JasminInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Linda A Jelicks
Wade Koba
Herbert B Tanowitz
Rosalia Mendez-Otero
Antonio C Campos de Carvalho
David C Spray
Albert Einstein College of Medicine · USUniversidade Federal do Rio de Janeiro · BR

Funding

Stem Cell Based Therapies in Chagasic CardiomyopathyR01HL073732 · NHLBI · YESHIVA UNIVERSITY · PI CAMPOS DE CARVALHO, ANTONIO CARLOS · 2003 to 2011
$3.2M
Interhemispheric Research/Training in Infectious DiseaseD43TW007129 · FIC · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI TANOWITZ, HERBERT BERNARD · 2004 to 2013
$1.7M
FIC NIH HHS D43 TW007129FIC NIH HHS D43-TW007129NHLBI NIH HHS R01 HL073732NHLBI NIH HHS R01 HL73732
6 · The paper itself

Abstract

backgroundChagas disease, resulting from infection with the parasite Trypanosoma cruzi (T. cruzi), is a major cause of cardiomyopathy in Latin America. Drug therapy for acute and chronic disease is limited. Stem cell therapy with bone marrow mesenchymal cells (MSCs) has emerged as a novel therapeutic option for cell death-related heart diseases, but efficacy of MSC has not been tested in Chagas disease. METHODS AND

resultsWe now report the use of cell-tracking strategies with nanoparticle labeled MSC to investigate migration of transplanted MSC in a murine model of Chagas disease, and correlate MSC biodistribution with glucose metabolism and morphology of heart in chagasic mice by small animal positron emission tomography (microPET). Mice were infected intraperitoneally with trypomastigotes of the Brazil strain of T. cruzi and treated by tail vein injection with MSC one month after infection. MSCs were labeled with near infrared fluorescent nanoparticles and tracked by an in vivo imaging system (IVIS). Our IVIS results two days after transplant revealed that a small, but significant, number of cells migrated to chagasic hearts when compared with control animals, whereas the vast majority of labeled MSC migrated to liver, lungs and spleen. Additionally, the microPET technique demonstrated that therapy with MSC reduced right ventricular dilation, a phenotype of the chagasic mouse model.

conclusionsWe conclude that the beneficial effects of MSC therapy in chagasic mice arise from an indirect action of the cells in the heart rather than a direct action due to incorporation of large numbers of transplanted MSC into working myocardium.

Indexed as

AnimalsBiological AvailabilityBone Marrow CellsBone Marrow TransplantationChagas CardiomyopathyDisease Models, AnimalLiverLungMaleMiceMyocardiumSpleenStaining and Labeling

Identifiers

PMID23272265
PMCPMC3521704
OpenAlexW2056474354

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.