Evidence map›Paper›PMID 36261464›Full record

ArticleNPJ Regenerative medicine2022

Enforced mesenchymal stem cell tissue colonization counteracts immunopathology.

David García-Bernal, Miguel Blanquer, Carlos M Martínez, Ana I García-Guillén, Ana M García-Hernández, M Carmen Algueró, Rosa Yáñez, María L Lamana, Jose M Moraleda, Robert Sackstein

Abstract read
In one paragraph

Article in NPJ Regenerative medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

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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.

David García-BernalHematopoietic Transplant and Cellular Therapy Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.ORCID http://orcid.org/0000-0001-6610-8442
Miguel BlanquerHematopoietic Transplant and Cellular Therapy Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.
Carlos M MartínezExperimental Pathology Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.ORCID http://orcid.org/0000-0003-3307-1326
Ana I García-GuillénExercise Physiology Department, Faculty of Health Sciences, San Antonio Catholic University of Murcia (UCAM), Murcia, Spain.ORCID http://orcid.org/0000-0002-1824-9272
Ana M García-HernándezHematopoietic Transplant and Cellular Therapy Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.
M Carmen AlgueróHematopoietic Transplant and Cellular Therapy Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.
Rosa YáñezHematopoietic Innovative Therapies Division, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBER-ER), Madrid, Spain.ORCID http://orcid.org/0000-0003-0132-3402
María L LamanaHematopoietic Innovative Therapies Division, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBER-ER), Madrid, Spain.
Jose M MoraledaHematopoietic Transplant and Cellular Therapy Unit, Instituto Murciano de Investigación Biosanitaria (IMIB)-Arrixaca, Murcia, Spain.ORCID http://orcid.org/0000-0001-9080-1466
Robert SacksteinDepartment of Translational Medicine, and the Translational Glycobiology Institute, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, USA. sackstein@fiu.edu.ORCID http://orcid.org/0000-0003-1757-891X

Funding

Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI13/00184Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) RD12/0019/0001Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) RD12/0019/0023Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) RD16/0011/0001
6 · The paper itself

Abstract

Mesenchymal stem/stromal cells (MSCs) are distributed within all tissues of the body. Though best known for generating connective tissue and bone, these cells also display immunoregulatory properties. A greater understanding of MSC cell biology is urgently needed because culture-expanded MSCs are increasingly being used in treatment of inflammatory conditions, especially life-threatening immune diseases. While studies in vitro provide abundant evidence of their immunomodulatory capacity, it is unknown whether tissue colonization of MSCs is critical to their ability to dampen/counteract evolving immunopathology in vivo. To address this question, we employed a murine model of fulminant immune-mediated inflammation, acute graft-versus-host disease (aGvHD), provoked by donor splenocyte-enriched full MHC-mismatched hematopoietic stem cell transplant. aGvHD induced the expression of E-selectin within lesional endothelial beds, and tissue-specific recruitment of systemically administered host-derived MSCs was achieved by enforced expression of HCELL, a CD44 glycoform that is a potent E-selectin ligand. Compared to mice receiving HCELL

Identifiers

PMID36261464
PMCPMC9582223

What OpenQuestion holds

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LicenceCC BY
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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.