Evidence map›Paper›PMID 40034706›Full record

ArticleFrontiers in immunology2025

Improving the therapeutic profile of MSCs: Cytokine priming reduces donor-dependent heterogeneity and enhances their immunomodulatory capacity.

Jaris Valencia, Rosa M Yáñez, Sandra Muntión, María Fernández-García, Jorge Diego Martín-Rufino, Agustín G Zapata, Juan A Bueren, Ángeles Vicente, Fermín Sánchez-Guijo

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
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  3. Transcriptomics Insights into Spinal Cord Injury for Therapy Development.International journal of molecular sciences · 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

9 authors.

Jaris Valencia *Department of Cell Biology, School of Medicine, Complutense University of Madrid, Madrid, Spain.
Rosa M Yáñez *RICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Sandra MuntiónRICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
María Fernández-GarcíaRICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Jorge Diego Martín-RufinoDivision of Hematology/Oncology, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, United States.
Agustín G ZapataRICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Juan A BuerenRICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Ángeles Vicente *Department of Cell Biology, School of Medicine, Complutense University of Madrid, Madrid, Spain.
Fermín Sánchez-Guijo *RICORS TERAV, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: MSCs exhibit regenerative, anti-inflammatory and immunomodulatory properties due to the large amount of cytokines, chemokines and growth factors they secrete. MSCs have been extensively evaluated in clinical trials, however, in some cases their therapeutic effects are variable. Therefore, strategies to improve their therapeutic potential, such as preconditioning with proinflammatory factors, have been proposed. Several priming approaches have provided non-conclusive results, and the duration of priming effects on MSC properties or their response to a second inflammatory stimulus have not been fully addressed. Methods: We have investigated the impact of triple cytokine priming in MSCs on their characterization and viability, their transcriptomic profile, the functionality of innate and acquired immune cells, as well as the maintenance of the response to priming over time, their subsequent responsiveness to a second inflammatory stimulus. Results: Priming MSCs with proinflammatory cytokines (CK-MSCs) do not modify the differentiation capacity of MSCs, nor their immunophenotype and viability. Moreover, cytokine priming enhances the anti-inflammatory and immunomodulatory properties of MSCs against NK and dendritic cells, while maintaining the same T cell immunomodulatory capacity as unstimulated MSCs. Thus, they decrease T-lymphocytes and NK cell proliferation, inhibit the differentiation and allostimulatory capacity of dendritic cells and promote the differentiation of monocytes with an immunosuppressive profile. In addition, we have shown for the first time that proinflammatory priming reduces the variability between different donors and MSC origins. Finally, the effect on CK-MSC is maintained over time and even after a secondary inflammatory stimulus. Conclusions: Cytokine-priming improves the therapeutic potential of MSCs and reduces inter-donor variability.

Indexed as

CytokinesImmunomodulationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationCell DifferentiationCells, CulturedDendritic CellsHumansKiller Cells, NaturalT-LymphocytesCytokinescytokinesheterogeneityimmunomodulationinnate immune systemmesenchymal stem cellsmesenchymal stromal cellsMSCspriming

Identifiers

PMID40034706
PMCPMC11872697

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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.