Evidence map›Paper›PMID 37226203›Full record

ArticleStem cell research & therapy2023

Mesenchymal stem/stromal cells-derived extracellular vesicles as a potentially more beneficial therapeutic strategy than MSC-based treatment in a mild metabolic osteoarthritis model.

Kelly Warmink, Jaqueline L Rios, Suzy Varderidou-Minasian, Marta Torres-Torrillas, Devin R van Valkengoed, Sabine Versteeg, Niels Eijkelkamp, Harrie Weinans, Nicoline M Korthagen, Magdalena J Lorenowicz

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 38 citations in OpenAlex.

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  12. From pathogenesis to therapy: extracellular vesicles in osteoarthritis.Frontiers in bioengineering and biotechnology · 2026
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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.

Kelly WarminkRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Jaqueline L RiosRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Suzy Varderidou-MinasianRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Marta Torres-TorrillasBioregenerative Medicine and Applied Surgery Research Group, Department of Animal Medicine and Surgery, CEU Cardenal Herrera University, CEU Universities, Valencia, Spain.
Devin R van ValkengoedRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Sabine VersteegCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, PO Box 85090, 3508 AB, Utrecht, The Netherlands.
Niels EijkelkampCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, PO Box 85090, 3508 AB, Utrecht, The Netherlands.
Harrie WeinansRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Nicoline M KorthagenRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Magdalena J LorenowiczRegenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands. lorenowicz@bprc.nl.ORCID 0000-0001-8420-2029
University Medical Center Utrecht · NLUtrecht University · NLUniversidad Cardenal Herrera CEU · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stromal/stem cells (MSCs) and MSC-derived extracellular vesicles (MSC-EVs) hold promise as a disease modifying treatment in osteoarthritis (OA). Obesity, and its associated inflammation, contribute to OA development and metabolic OA represents a specific and significant group of the OA patient population. Given their immunomodulatory properties, MSC and MSC-EVs are especially interesting for this group of patients as a therapeutic option. Here, we were the first to compare the therapeutic efficacy of MSCs and MSC-EVs in a mild OA model taking these metabolic aspects into consideration.

methodsMale Wistar-Han rats (Crl:WI(Han) (n = 36) were fed a high fat diet for 24 weeks, with unilateral induction of OA by groove surgery after 12 weeks. Eight days after surgery rats were randomized in three treatment groups receiving MSCs, MSC-EVs or vehicle injection. Pain-associated behavior, joint degeneration, and local and systemic inflammation were measured.

resultsWe demonstrated that despite not having a significant therapeutic effect, MSC-EV treatment results in lower cartilage degeneration, less pain behaviour, osteophytosis and joint inflammation, than MSC treatment. Suggesting that MSC-EVs could be a more promising therapeutic strategy than MSCs in this mild metabolic OA model.

conclusionIn summary, we find that MSC treatment has negative effects on the joint in metabolic mild OA. This is an essential finding for the significant group of patients with metabolic OA phenotype, and might help to understand why clinical translation of MSC treatment shows varying therapeutic efficacy thus far. Our results also suggest that MSC-EV-based treatment might be a promising option for these patients, however MSC-EV therapeutic efficacy will need improvement.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsOsteoarthritisAnimalsHumansInflammationMalePainRatsRats, WistarCartilage regenerationExtracellular vesiclesInflammationMesenchymal stem/stromal cellsOsteoarthritisRat high fat diet groove model

Identifiers

PMID37226203
PMCPMC10210425
OpenAlexW4378173543

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.