Evidence map›Paper›PMID 40047974›Full record

ReviewAngiogenesis2025

Immune-privileged cord blood-derived endothelial colony-forming cells: advancing immunomodulation and vascular regeneration.

David M Smadja, Yanis Berkane, Nun K Bentounes, Jeanne Rancic, Audrey Cras, Cécile Pinault, Marie Ouarne, Elise Paucod, Walid Rachidi, Alexandre G Lellouch and 1 more

Abstract readReview
In one paragraph

Review in Angiogenesis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

11 authors.

David M SmadjaUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Center, Paris, France. david.smadja@aphp.fr.
Yanis BerkaneDepartment of Plastic, Reconstructive and Aesthetic Surgery, Hôpital Sud, CHU Rennes, University of Rennes, Rennes, France.
Nun K BentounesUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Center, Paris, France.
Jeanne RancicUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Center, Paris, France.
Audrey CrasCell Therapy Department, AP-HP, Saint-Louis Hospital, Paris, F-75010, France.
Cécile PinaultUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Center, Paris, France.
Marie OuarneUniv. Grenoble Alpes, CEA, INSERM, IRIG-BGE UA13, Grenoble, 38000, France.
Elise PaucodUniv. Grenoble Alpes, CEA, INSERM, IRIG-BGE UA13, Grenoble, 38000, France.
Walid RachidiUniv. Grenoble Alpes, CEA, INSERM, IRIG-BGE UA13, Grenoble, 38000, France.
Alexandre G LellouchUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Center, Paris, France.
Maxime JeljeliDepartment of Plastic, Reconstructive and Aesthetic Surgery, Cedars Sinai Hospital, Los Angeles, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cord blood-derived endothelial colony-forming cells (CB-ECFCs) hold significant promise for regenerative medicine due to their unique vasculogenic and immunomodulatory properties. These cells exhibit a superior proliferative capacity, robust ability to form vascular networks, and lower immunogenicity compared to adult and embryonic stem cell-derived counterparts. The immune-privileged characteristics of CB-ECFCs, including reduced expression of pro-inflammatory mediators and tolerance-inducing molecules such as HLA-G, further enhance their therapeutic potential. Their low immunogenicity minimizes the risk of immune rejection, making them suitable for allogenic cell therapies. Their application extends to complex tissue engineering and organ revascularization, where their ability to integrate into three-dimensional scaffolds and support vascular tree formation represents a significant advancement. Moreover, CB-ECFCs' capability to adapt to inflammatory stimuli and retain immunological memory highlights their functional versatility in dynamic microenvironments. This review highlights the remarkable ontogeny of ECFCs while unveiling the unparalleled potential of CB-ECFCs in revolutionizing regenerative medicine. From pre-vascularizing engineered tissues and organoids to pioneering cell-based therapies for cardiovascular, dermatological, and degenerative diseases, CB-ECFCs stand at the forefront of cutting-edge biomedical advancements, offering unprecedented opportunities for therapeutic innovation. By leveraging their vasculogenic, immune-regulatory, and regenerative capacities, CB-ECFCs offer a robust alternative for addressing the challenges of vascular repair and organ engineering. Future research should focus on unraveling their transcriptomic and functional profiles to optimize clinical applications and advance the field of regenerative medicine.

Indexed as

Endothelial CellsEndothelial Progenitor CellsFetal BloodImmune PrivilegeImmunomodulationNeovascularization, PhysiologicRegenerationAnimalsHumansRegenerative MedicineTissue EngineeringArtificial skinECFCEndothelial cellsImmunogenicityImmunomodulationOrganoidRegeneration

Identifiers

PMID40047974
PMCPMC11885380

What OpenQuestion holds

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Registered trials

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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.