Evidence map›Paper›PMID 28441721›Full record

ReviewInternational journal of molecular sciences2017

Pathogenic or Therapeutic Extracellular Vesicles in Rheumatic Diseases: Role of Mesenchymal Stem Cell-Derived Vesicles.

Stella Cosenza, Maxime Ruiz, Marie Maumus, Christian Jorgensen, Danièle Noël

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
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  8. Biomedical Application of MSCs in Corneal Regeneration and Repair.International journal of molecular sciences · 2025
    Review
  9. Bioinspired exosome-SiOTheranostics · 2025
    Article
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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

5 authors at 1 institution in 1 country.

Stella CosenzaInstitute of Regenerative Medicine and Biotherapies, INSERM, University of Montpellier, 34090 Montpellier, France. stella.cosenza@inserm.fr.
Maxime RuizInstitute of Regenerative Medicine and Biotherapies, INSERM, University of Montpellier, 34090 Montpellier, France. maxime.ruiz@inserm.fr.
Marie MaumusInstitute of Regenerative Medicine and Biotherapies, INSERM, University of Montpellier, 34090 Montpellier, France. marie.maumus@inserm.fr.
Christian JorgensenInstitute of Regenerative Medicine and Biotherapies, INSERM, University of Montpellier, 34090 Montpellier, France. christian.jorgensen@inserm.fr.
Danièle NoëlInstitute of Regenerative Medicine and Biotherapies, INSERM, University of Montpellier, 34090 Montpellier, France. daniele.noel@inserm.fr.
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) are important mediators of cell-to-cell communication pathways via the transport of proteins, mRNA, miRNA and lipids. There are three main types of EVs, exosomes, microparticles and apoptotic bodies, which are classified according to their size and biogenesis. EVs are secreted by all cell types and their function reproduces that of the parental cell. They are involved in many biological processes that regulate tissue homeostasis and physiopathology of diseases. In rheumatic diseases, namely osteoarthritis (OA) and rheumatoid arthritis (RA), EVs have been isolated from synovial fluid and shown to play pathogenic roles contributing to progression of both diseases. By contrast, EVs may have therapeutic effect via the delivery of molecules that may stop disease evolution. In particular, EVs derived from mesenchymal stem cells (MSCs) reproduce the main functions of the parental cells and therefore represent the ideal type of EVs for modulating the course of either disease. The aim of this review is to discuss the role of EVs in OA and RA focusing on their potential pathogenic effect and possible therapeutic options. Special attention is given to MSCs and MSC-derived EVs for modulating OA and RA progression with the perspective of developing innovative therapeutic strategies.

Indexed as

AnimalsArthritis, RheumatoidCell-Derived MicroparticlesExosomesExtracellular VesiclesHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationOsteoarthritiscell therapyexosomeextracellular vesiclemesenchymal stem cellmicroparticleosteoarthritisrheumatoid arthritis

Identifiers

PMID28441721
PMCPMC5412468
OpenAlexW2608190391

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.