Evidence map›Paper›PMID 41580705›Full record

ReviewJournal of translational medicine2026

Critical evaluation of compositions and clinical relevance of Wharton's jelly-derived biologics.

Annette M Marleau, Jocelynn R Pearl, Patricia Juarez, Paloma Almeida, Sara Miguel, Erendira Olvera Felix, Francesco M Marincola, Rachel West, Lee Howard, Diego Guerena and 1 more

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Annette M MarleauImmune Advisors, San Diego, CA, 92122, USA. annette.marleau@gmail.com.ORCID 0009-0008-7287-0335
Jocelynn R PearlTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.
Patricia JuarezCenter for Scientific Research and Higher Education at Ensenada, Ensenada, Baja California, 22860, Mexico.
Paloma AlmeidaTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.
Sara MiguelTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.
Erendira Olvera FelixCenter for Scientific Research and Higher Education at Ensenada, Ensenada, Baja California, 22860, Mexico.
Francesco M MarincolaTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.
Rachel WestLongevity LA, Los Angeles, CA, 90025, USA.
Lee HowardCompass Human Performance, Nashville, TN, 37205, USA.
Diego GuerenaTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.
Edward ClayTranslational and Advanced Medical (TAM) Global, Nashville, TN, 37011, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWharton’s jelly, the mucoid connective tissue that surrounds umbilical cord vessels, contains both acellular and cellular components with recognized relevance to regenerative medicine. The acellular extracellular matrix (ECM) is composed of collagen fibers, hyaluronic acid, proteoglycans, glycosaminoglycans, that provides a scaffold for bioactive molecules such as growth factors and cytokines that support structural integrity and tissue repair. The cellular component of native Wharton’s jelly consists primarily of multipotent mesenchymal stromal cells (MSCs), which are leveraged in regenerative medicine for their differentiation capacity, trophic signaling, angiogenic activity, and immune modulatory activities. There is a growing commercial market for injectable, minimally manipulated Wharton’s jelly allograft products for clinical use to provide structural support or cushioning. Although these products comprise ECM, they are often presumed or represented to also contain viable MSCs capable of providing therapeutic benefit.

methodsA comprehensive literature review was performed, examining published data on the biologic components of Wharton’s jelly and common methods of processing and utilizing this tissue as a source of ECM or MSC-based therapeutics. Empirical laboratory analyses were also conducted on minimally manipulated Wharton’s jelly tissue products to microscopically quantify total cell content, viable cell counts, and to assess the percentages of MSCs by flow cytometry.

resultsPublished literature shows that ECM-based preparations can support endogenous repair processes or serve as scaffolds in tissue engineering, but they do not contain therapeutically meaningful quantities of viable primary MSCs. To achieve any measurable biological or clinical effect using MSCs, administration of MSCs at defined therapeutic doses is required, typically ≥10 million MSCs for local delivery and 70–190 million cells for systemic infusion. These doses can only be obtained by intentionally isolating MSCs from fresh Wharton’s jelly tissue and subsequently expanding them in vitro. Indeed, our analyses of minimally manipulated Wharton’s jelly product samples show that these materials contain ECM with only trace levels of residual cells. Total cell counts in Wharton’s jelly tissue preparations ranged from 3,369 to 111,170 cells per cubic centimeter, with 0–19.1% viability, and only rare viable MSCs.

conclusionsMinimally manipulated Wharton’s jelly products should be viewed as acellular ECM preparations, comprising negligible MSCs and lacking the capacity to provide cell-mediated therapeutic benefits. An understanding of the compositions of ECM products and true MSC-based therapies is essential to ensure appropriate clinical use and responsible integration into regenerative medicine practices.

Indexed as

Biological ProductsWharton JellyAnimalsExtracellular MatrixHumansMesenchymal Stem CellsRegenerative MedicineBiological ProductsCell therapyExtracellular matrixMesenchymal stem cellsRegenerative medicineWharton’s jelly

Identifiers

PMID41580705
PMCPMC12903654

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.