Evidence map›Paper›PMID 42045131›Full record

ArticleStem cells translational medicine2026

Moderate neuroprotection of combination cell therapy in fetal growth restricted newborns at postnatal day 10.

Kirat K Chand, Kate Beecher, Rachel Nano, Seen-Ling Sim, Jane Sun, Peytn Stokes-Marshall, Lillian Macfarlane, John Luff, Hannah Musco, Paul B Colditz and 3 more

Abstract read
In one paragraph

Article in Stem cells 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

13 authors.

Kirat K ChandUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
Kate BeecherUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.ORCID 0000-0001-7462-1158
Rachel NanoFrazer Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Seen-Ling SimFrazer Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Jane SunFrazer Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Peytn Stokes-MarshallUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
Lillian MacfarlaneUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
John LuffUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
Hannah MuscoUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
Paul B ColditzUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.
Kiarash KhosrotehraniFrazer Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Jatin PatelFrazer Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Julie A WixeyUQ Centre for Clinical Research, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD 4029, Australia.ORCID 0000-0002-9716-8170

Funding

National Heart Foundation of Australia
6 · The paper itself

Abstract

Infants with fetal growth restriction (FGR) are at increased risk of adverse neurodevelopmental conditions, including motor, learning, and behavioral deficits. There are currently no treatments to protect the FGR newborn from lifelong neurological conditions. We have previously reported neuroprotective potential of a single dose of combined mesenchymal stromal cells and endothelial colony-forming cells (ECFCs) therapy, termed cECFC, isolated from healthy human term placenta, in treating brain injury in a preclinical model of FGR. We administered cECFCs to newborn FGR pigs and survived to postnatal day 4 (2-week human equivalence). We reported improved gray and white matter integrity, reduced glial-mediated inflammation and improved microvasculature. Here, we aimed to examine whether this novel therapy presented sustained efficacy in newborn pigs that survived to postnatal day 10 (1-month human equivalence). We determined a single dose of cECFC treatment affords moderate neuroprotective capacity in the cortex but limited efficacy in the periventricular white matter. We also report minimal modulation of the inflammatory environment, with ongoing glial activation observed in most regions examined. Our data suggest a diminution in efficacy of single-dose cECFC 10 days after administration. We propose multiple doses of cECFCs may be required to maintain neuroprotective capacity during early post-natal life in FGR newborns. Overall, these findings demonstrate the importance of extended pre-clinical studies to determine the efficacy of treatments prior to translation to clinical trials.

Indexed as

Cell- and Tissue-Based TherapyFetal Growth RetardationMesenchymal Stem CellsNeuroprotectionAnimalsAnimals, NewbornFemaleHumansInfant, NewbornPregnancySwinebrain injuryfetal growth restrictionneonatestem cells

Identifiers

PMID42045131
PMCPMC13120858

What OpenQuestion holds

Textmetadata
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.