Evidence map›Paper›PMID 40558383›Full record

ArticleStem cells translational medicine2025

Amniotic fluid collected from vaginal birth as a source of stem cells for clinical applications and disease modeling.

Mallory L Lennon, Amy Frieman, Alyssa K Salazar, Igor Kogut, Ganna Bilousova, Jeffrey G Jacot

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 3D Bioprinting of Blood Vessel Model for Improving Wound Healing.International journal of molecular sciences · 2026
    Article
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

6 authors.

Mallory L LennonDepartment of Bioengineering, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States.
Amy FriemanDepartment of Dermatology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, United States.
Alyssa K SalazarDepartment of Bioengineering, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States.
Igor KogutDepartment of Dermatology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, United States.
Ganna BilousovaDepartment of Dermatology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, United States.
Jeffrey G JacotDepartment of Bioengineering, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States.ORCID 0000-0002-1272-5055

Funding

NRSA Training CoreTL1TR002533 · NCATS · UNIVERSITY OF COLORADO DENVER · PI CICUTTO, LISA · 2018 to 2022
$3.0M
UC Denver MARC U*STAR Scholars Program SupplementT34GM096958 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ALLEN, RICHARD M, FLORES, SONIA CASTRO · 2013 to 2022
$2.3M
PRE-VASCULARIZED AND DEGRADABLE PATCHES FOR CORRECTION OF CONGENITAL HEART DEFECTSR01HL130436 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI JACOT, JEFFREY G · 2016 to 2020
$2.0M
MicroRNA-based purification of keratinocytes derived from pluripotent stem cells for the treatment of skin diseasesR21AR074642 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI BILOUSOVA, GANNA · 2019 to 2020
$376k
Children's Hospital ColoradoColorado Clinical and Translational Sciences Institute 5TL1TR002533-02Dystrophic Epidermolysis Bullosa Research AssociationGates Grubstake FundGates Institute for Regenerative MedicineNational Science Foundation Graduate Research Fellowship Program DGE-1553798NCATS NIH HHS TL1 TR002533NHLBI NIH HHS R01 HL130436NIAMS NIH HHS R21 AR074642NIGMS NIH HHS T34 GM096958NIH HHS R01HL130436NIH HHS R21 AR074642
6 · The paper itself

Abstract

importanceAmniotic fluid is a promising source of autologous cells for disease modeling, drug screening, and regenerative medicine applications. However, current methods of collecting amniotic fluid are invasive, and samples are limited to pregnancies that require amniocentesis or cesarean section.

objectiveThe purpose of this study was to determine whether amniotic fluid cells could be isolated and cultured from amniotic fluid collected during vaginal deliveries.

interventionAmniotic fluid samples were obtained during delivery of 4 neonates, 3 of which had been prenatally diagnosed with hypoplastic left heart syndrome (HLHS) in utero. Adherent amniotic fluid cells were assessed for maternal cell contamination, proliferation rate, surface marker expression, and differentiation potential. Amniotic fluid cells were also reprogrammed to induced pluripotent stem cells (iPSCs) and differentiated into functional cardiomyocytes.

resultsAmniotic fluid cells collected from vaginal deliveries showed similar surface marker phenotype and differentiation characteristics to amniotic fluid-derived mesenchymal stem cells collected from amniocentesis and cesarean section. Amniotic fluid cells collected during vaginal births of both neonates with HLHS and one neonate with typical heart geometry could be reprogrammed to iPSCs and differentiated to a cardiac lineage with high efficiency. Conclusions and Relevence: These findings suggest that amniotic fluid collected from vaginal births is a readily available source of patient-specific stem cells for banking, in vitro disease modeling, and regenerative medicine applications.

Indexed as

Amniotic FluidInduced Pluripotent Stem CellsAdultAmniocentesisCell DifferentiationCells, CulturedFemaleHumansInfant, NewbornMyocytes, CardiacPregnancyamniotic fluidcongenital heart defectsmesenchymal stem cellsstem cellsvaginal birth

Identifiers

PMID40558383
PMCPMC12188528

What Socratic holds

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LicenceCC BY
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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 Socratic graph.