Evidence map›Paper›PMID 30713713›Full record

ArticleBMJ open respiratory research2019

Cell therapy for ARDS: efficacy of endobronchial versus intravenous administration and biodistribution of MAPCs in a large animal model.

Nayra Cardenes, Paola Aranda-Valderrama, Jonathan P Carney, Jacobo Sellares Torres, Diana Alvarez, Ergin Kocyildirim, Julie A Wolfram Smith, Antony E Ting, Luigi Lagazzi, Zheming Yu and 4 more

Erratum issuedAbstract read
In one paragraph

Article in BMJ open respiratory research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  8. Exploring pulmonary distribution of intratracheally instilled liquid foams in excised porcine lungs.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Nayra Cardenes *The Dorothy P. and Richard P. Simmons Center for Interstitial Lung Diseases, Pittsburgh, Pennsylvania, USA.
Paola Aranda-Valderrama *The Dorothy P. and Richard P. Simmons Center for Interstitial Lung Diseases, Pittsburgh, Pennsylvania, USA.
Jonathan P CarneyDepartment of Radiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Jacobo Sellares TorresThe Dorothy P. and Richard P. Simmons Center for Interstitial Lung Diseases, Pittsburgh, Pennsylvania, USA.
Diana AlvarezThe Dorothy P. and Richard P. Simmons Center for Interstitial Lung Diseases, Pittsburgh, Pennsylvania, USA.
Ergin KocyildirimDepartment of Cardiothoracic Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Julie A Wolfram SmithCardiopulmonary Program at Athersys, Inc, Cleveland, Ohio, USA.
Antony E TingCardiopulmonary Program at Athersys, Inc, Cleveland, Ohio, USA.
Luigi LagazziDepartment of Cardiothoracic Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Zheming YuDepartment of Radiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Scott MasonDepartment of Radiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Ernesto SantosDepartment of Radiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Brian J LoprestiDepartment of Radiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Mauricio RojasThe Dorothy P. and Richard P. Simmons Center for Interstitial Lung Diseases, Pittsburgh, Pennsylvania, USA.

Funding

Aging of Mesenchymal Stem Cells Missing Link in IPFR01HL123766 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROJAS, MAURICIO · 2015 to 2018
$1.9M
Cell Therapy for the Treatment of Acute Respiratory Distress SyndromeR42AA024003 · NIAAA · ATHERSYS, INC. · PI ROJAS, MAURICIO, TING, ANTHONY · 2014 to 2017
$968k
NHLBI NIH HHS R01 HL123766NIAAA NIH HHS R42 AA024003
6 · The paper itself

Abstract

Introduction: Bone marrow-derived multipotent adult progenitor cells (MAPCs) are adult allogeneic adherent stem cells currently investigated clinically for use in acute respiratory distress syndrome (ARDS). To date, there is no agreement on which is the best method for stem cells delivery in ARDS. Here, we compared the efficacy of two different methods of administration and biodistribution of MAPC for the treatment of ARDS in a sheep model. Methods: MAPC were labelled with [ Results: The distribution and retention of the MAPC was dependent on the method of cell administration. By EB route, PET images showed that MAPC remained at the site of administration and no changes were observed after 5 hours, whereas with intravenous route, the cells had broad biodistribution to different organs, being the lung the main organ of retention at 1 and 5 hours. MAPC demonstrated an equal effect on arterial oxygenation recovery by either route of administration. Conclusion: The EB or intravenous routes of administration of MAPC are both effective for the treatment of ARDS in an acute sheep model, and the effect of MAPC therapy is not dependent of parenchymal integration or systemic biodistribution.

Indexed as

Adult Stem CellsAnimalsBronchiCells, CulturedDisease Models, AnimalFemaleHumansInfusions, IntravenousLipopolysaccharidesMaleMultipotent Stem CellsPositron Emission Tomography Computed TomographyPrimary Cell CultureRespiratory Distress SyndromeSheepTreatment OutcomeLipopolysaccharidesAcute Respiratory Distress Syndrome (ARDS)lung injuryMesenchymal stem cell (MSC)Multipotent Adult Progenitor Cells (MAPC)

Identifiers

PMID30713713
PMCPMC6339992

What OpenQuestion holds

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Registered trials

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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.