Evidence map›Paper›PMID 31370879›Full record

ArticleStem cell research & therapy2019

Mesenchymal stem cell repression of Th17 cells is triggered by mitochondrial transfer.

Patricia Luz-Crawford, Javier Hernandez, Farida Djouad, Noymar Luque-Campos, Andres Caicedo, Séverine Carrère-Kremer, Jean-Marc Brondello, Marie-Luce Vignais, Jérôme Pène, Christian Jorgensen

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 132 citations in OpenAlex.

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31 more citing papers are in PubMed but not listed here.

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 6 institutions in 3 countries.

Patricia Luz-CrawfordLaboratorio de Inmunología Celular y Molecular, Centro de Investigación Biomédica, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Javier HernandezIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Farida DjouadIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Noymar Luque-CamposLaboratorio de Inmunología Celular y Molecular, Centro de Investigación Biomédica, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Andres CaicedoUniversidad San Francisco de Quito, Hospital de los Valles, Quito, Ecuador.
Séverine Carrère-KremerIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Jean-Marc BrondelloIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Marie-Luce VignaisIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Jérôme PèneIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France.
Christian JorgensenIRMB, Univ Montpellier, INSERM, Hôpital Saint-Eloi, 80 avenue Augustin Fliche, 34295, Montpellier CEDEX 5, France. christian.jorgensen@inserm.fr.
Inserm · FRHôpital Saint Eloi · FRUniversidad de Los Andes, Chile · CLCentre Hospitalier Universitaire de Montpellier · FRUniversidad San Francisco de Quito · ECUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) are multipotent cells with broad immunosuppressive capacities. Recently, it has been reported that MSCs can transfer mitochondria to various cell types, including fibroblast, cancer, and endothelial cells. It has been suggested that mitochondrial transfer is associated with a physiological response to cues released by damaged cells to restore and regenerate damaged tissue. However, the role of mitochondrial transfer to immune competent cells has been poorly investigated. METHODS AND

resultsHere, we analyzed the capacity of MSCs from the bone marrow (BM) of healthy donors (BM-MSCs) to transfer mitochondria to primary CD4

conclusionsThe present study brings some insights into a novel mechanism of T cell function regulation through mitochondrial transfer from stromal stem cells. The reduced mitochondrial transfer by RA-sMSCs might contribute to the persistence of chronic inflammation in RA synovitis.

Indexed as

Arthritis, RheumatoidBone Marrow CellsCells, CulturedCoculture TechniquesHumansInterleukin-17Mesenchymal Stem CellsMitochondriaOxygen ConsumptionSynovial MembraneTh17 CellsT-Lymphocytes, RegulatoryTumor Necrosis Factor-alphaInterleukin-17Tumor Necrosis Factor-alphaImmunomodulationMesenchymal stem cellsMitochondria transferT cellTh17

Identifiers

PMID31370879
PMCPMC6676586
OpenAlexW2964578086

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.