Evidence map›Paper›PMID 24825538›Full record

ArticleJournal of medical primatology2014

Comparisons of phenotype and immunomodulatory capacity among rhesus bone-marrow-derived mesenchymal stem/stromal cells, multipotent adult progenitor cells, and dermal fibroblasts.

Gregory M Sindberg, Beth A Lindborg, Qi Wang, Christina Clarkson, Melanie Graham, Robert Donahue, Bernhard J Hering, Catherine M Verfaillie, Pratima Bansal-Pakala, Timothy D O'Brien

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of medical primatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 17% 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, 16 citations in OpenAlex.

  1. Review
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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 at 3 institutions in 2 countries.

Gregory M Sindberg *Department of Surgery, University of Minnesota, St. Paul, MN, USA.
Beth A Lindborg *Veterinary Population Medicine Department, University of Minnesota, St. Paul, MN, USA.
Qi WangBiostatistical Design and Analysis Center, Clinical and Translational Science Institute, University of Minnesota, St. Paul, MN, USA.
Christina ClarksonStem Cell Institute, University of Minnesota, St. Paul, MN, USA.
Melanie GrahamDepartment of Surgery, University of Minnesota, St. Paul, MN, USA.
Robert DonahueHematology Branch, National Heart Lung Blood Institute, Rockville, MD, USA.
Bernhard J HeringDepartment of Surgery, University of Minnesota, St. Paul, MN, USA.
Catherine M VerfaillieStem Cell Institute, University of Leuven, Leuven, Belgium.
Pratima Bansal-PakalaDepartment of Surgery, University of Minnesota, St. Paul, MN, USA.
Timothy D O'BrienVeterinary Population Medicine Department, University of Minnesota, St. Paul, MN, USA.
University of Minnesota · USKU Leuven · BENational Heart Lung and Blood Institute · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Retroviral Mediated Gene Transfer Into Primate Hematopoietic CellsZICHL002338 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DONAHUE, ROBERT E · 2010 to 2018
$30.5M
Intramural NIH HHS Z99 HL999999Intramural NIH HHS ZIC HL002338NCATS NIH HHS UL1 TR002494NIH HHS P51 OD011107
6 · The paper itself

Abstract

backgroundPotent immunomodulatory effects have been reported for mesenchymal stem/stromal cells (MSCs), multipotent adult progenitor cells (MAPCs), and fibroblasts. However, side-by-side comparisons of these cells specifically regarding immunophenotype, gene expression, and suppression of proliferation of CD4(+) and CD8(+) lymphocyte populations have not been reported.

methodsWe developed MAPC and MSC lines from rhesus macaque bone marrow and fibroblast cell lines from rhesus dermis and assessed phenotypes based upon differentiation potential, flow cytometric analysis of immunophenotype, and quantitative RT-PCR analysis of gene expression. Using allogeneic lymphocyte proliferation assays, we compared the in vitro immunomodulatory potency of each cell type. RESULTS AND

conclusionsExtensive phenotypic similarities exist among each cell type, although immunosuppressive potencies are distinct. MAPCs are most potent, and fibroblasts are the least potent cell type. All three cell types demonstrated immunomodulatory capacity such that each may have potential therapeutic applications such as in organ transplantation, where reduced local immune response is desirable.

Indexed as

Immunosuppression TherapyAdult Stem CellsAnimalsBone Marrow CellsCell LineFemaleFibroblastsMacaca mulattaMaleMesenchymal Stem CellsPhenotypeSkincellular therapyimmunophenotypeT-cell suppression

Identifiers

PMID24825538
PMCPMC4699285
OpenAlexW2041169877

What OpenQuestion holds

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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.