Evidence map›Paper›PMID 33810359›Full record

ArticleInternational journal of molecular sciences2021

HIF-1α and Pro-Inflammatory Signaling Improves the Immunomodulatory Activity of MSC-Derived Extracellular Vesicles.

Marta Gómez-Ferrer, Estela Villanueva-Badenas, Rafael Sánchez-Sánchez, Christian M Sánchez-López, Maria Carmen Baquero, Pilar Sepúlveda, Akaitz Dorronsoro

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-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

41 citing papers in PubMed, 58 citations in OpenAlex.

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  9. Isolation methods of exosomes derived from dental stem cells.International journal of oral science · 2025
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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

7 authors at 3 institutions in 1 country.

Marta Gómez-FerrerRegenerative Medicine and Heart Transplantation Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Estela Villanueva-BadenasRegenerative Medicine and Heart Transplantation Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0001-5185-7598
Rafael Sánchez-SánchezRegenerative Medicine and Heart Transplantation Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Christian M Sánchez-LópezÀrea de Parasitologia, Departament de Farmàcia i Tecnologia Farmacèutica i Parasitologia, Universitat de València, Av. V.A. Estellés s/n, 46100 Valencia, Spain.ORCID 0000-0001-6062-5940
Maria Carmen BaqueroServicio de Cirugía Oral y Maxilofacial, Hospital Universitari I Politècnic La Fe, Avenida, Fernando Abril Martorell, 106, 46026 Valencia, Spain.
Pilar SepúlvedaRegenerative Medicine and Heart Transplantation Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0001-6071-7431
Akaitz DorronsoroRegenerative Medicine and Heart Transplantation Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0001-6141-8484
Instituto de Investigación Sanitaria La Fe · ESHospital Universitari i Politècnic La Fe · ESUniversitat de València · ES

Funding

Conselleria de Innovación, Universidades, Ciencia y Sociedad Digital, Generalitat Valenciana ACIF/2017/318Conselleria de Innovación, Universidades, Ciencia y Sociedad Digital, Generalitat Valenciana ACIF/2018/254Instituto de Salud Carlos III PI16/00107Instituto de Salud Carlos III PI19/00245Instituto de Salud Carlos III RD16/0011/0004
6 · The paper itself

Abstract

Despite the strong evidence for the immunomodulatory activity of mesenchymal stromal cells (MSCs), clinical trials have so far failed to clearly show benefit, likely reflecting methodological shortcomings and lack of standardization. MSC-mediated tissue repair is commonly believed to occur in a paracrine manner, and it has been stated that extracellular vesicles (EVs) secreted by MSCs (EVMSC) are able to recapitulate the immunosuppressive properties of parental cells. As a next step, clinical trials to corroborate preclinical studies should be performed. However, effective dose in large mammals, including humans, is quite high and EVs industrial production is hindered by the proliferative senescence that affects MSCs during massive cell expansion. We generated a genetically modified MSC cell line overexpressing hypoxia-inducible factor 1-alpha and telomerase to increase the therapeutic potency of EVMSC and facilitate their large-scale production. We also developed a cytokine-based preconditioning culture medium to prime the immunomodulatory response of secreted EVs (EV

Indexed as

ImmunomodulationAnimalsCell LineCell ProliferationCells, CulturedCytokinesDental PulpExtracellular VesiclesGenetic VectorsGreen Fluorescent ProteinsHumansHypersensitivity, DelayedHypoxia-Inducible Factor 1, alpha SubunitLentivirusMaleMesenchymal Stem CellsCytokinesGreen Fluorescent ProteinsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitRecombinant ProteinsTelomeraseextracellular vesicleshypoxia-inducible factor 1-alphaimmunomodulationmesenchymal stromal cellsT-cells

Identifiers

PMID33810359
PMCPMC8036951
OpenAlexW3148496375

What OpenQuestion holds

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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.