Evidence map›Paper›PMID 29650593›Full record

ArticleStroke2018

Human Neural Stem Cell Extracellular Vesicles Improve Recovery in a Porcine Model of Ischemic Stroke.

Robin L Webb, Erin E Kaiser, Brian J Jurgielewicz, Samantha Spellicy, Shelley L Scoville, Tyler A Thompson, Raymond L Swetenburg, David C Hess, Franklin D West, Steven L Stice

Open access · greenAbstract read
In one paragraph

Article in Stroke, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed, 3 pooled it
10.7field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 3 syntheses or guidelines pooled it, 222 citations in OpenAlex.

  1. Pooled it
  2. Exosomes in pathogenesis, diagnosis, and therapy of ischemic stroke.Frontiers in bioengineering and biotechnology · 2022
    Pooled it
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  19. Stem cell and gene therapies for leukodystrophies.Molecular therapy. Methods & clinical development · 2025
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86 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 3 countries.

Robin L WebbFrom the ArunA Biomedical, Athens, GA (R.L.W., S.L. Scoville, T.A.T., R.L.S).
Erin E KaiserRegenerative Bioscience Center (R.L.W., E.E.K., B.J.J., S.S., F.D.W., S.L. Stice).
Brian J JurgielewiczRegenerative Bioscience Center (R.L.W., E.E.K., B.J.J., S.S., F.D.W., S.L. Stice).
Samantha SpellicyRegenerative Bioscience Center (R.L.W., E.E.K., B.J.J., S.S., F.D.W., S.L. Stice).
Shelley L ScovilleFrom the ArunA Biomedical, Athens, GA (R.L.W., S.L. Scoville, T.A.T., R.L.S).
Tyler A ThompsonFrom the ArunA Biomedical, Athens, GA (R.L.W., S.L. Scoville, T.A.T., R.L.S).
Raymond L SwetenburgFrom the ArunA Biomedical, Athens, GA (R.L.W., S.L. Scoville, T.A.T., R.L.S).
David C HessUniversity of Georgia, Rhodes Center for Animal and Dairy Science, Athens; and Department of Neurology, Augusta University, GA (D.C.H.).
Franklin D WestRegenerative Bioscience Center (R.L.W., E.E.K., B.J.J., S.S., F.D.W., S.L. Stice).
Steven L SticeRegenerative Bioscience Center (R.L.W., E.E.K., B.J.J., S.S., F.D.W., S.L. Stice) sstice@arunabiomedical.com.
Regenerative Medicine Institute · MXAruna Biomedical (United States) · US

Funding

Combined Nanoparticle and Neural Stem Cell Therapies in a Pig Model of StrokeR01NS093314 · NINDS · UNIVERSITY OF GEORGIA · PI WEST, FRANKLIN D · 2015 to 2019
$2.4M
Human Neural Cell Exosomes as a therapeutic treatment for strokeR43NS103596 · NINDS · ARUNA BIOMEDICAL, INC. · PI WEBB, ROBIN L · 2017 to 2017
$500k
NINDS NIH HHS R01 NS093314NINDS NIH HHS R43 NS103596
6 · The paper itself

Abstract

background and purposeRecent work from our group suggests that human neural stem cell-derived extracellular vesicle (NSC EV) treatment improves both tissue and sensorimotor function in a preclinical thromboembolic mouse model of stroke. In this study, NSC EVs were evaluated in a pig ischemic stroke model, where clinically relevant end points were used to assess recovery in a more translational large animal model.

methodsIschemic stroke was induced by permanent middle cerebral artery occlusion (MCAO), and either NSC EV or PBS treatment was administered intravenously at 2, 14, and 24 hours post-MCAO. NSC EV effects on tissue level recovery were evaluated via magnetic resonance imaging at 1 and 84 days post-MCAO. Effects on functional recovery were also assessed through longitudinal behavior and gait analysis testing.

resultsNSC EV treatment was neuroprotective and led to significant improvements at the tissue and functional levels in stroked pigs. NSC EV treatment eliminated intracranial hemorrhage in ischemic lesions in NSC EV pigs (0 of 7) versus control pigs (7 of 8). NSC EV-treated pigs exhibited a significant decrease in cerebral lesion volume and decreased brain swelling relative to control pigs 1-day post-MCAO. NSC EVs significantly reduced edema in treated pigs relative to control pigs, as assessed by improved diffusivity through apparent diffusion coefficient maps. NSC EVs preserved white matter integrity with increased corpus callosum fractional anisotropy values 84 days post-MCAO. Behavior and mobility improvements paralleled structural changes as NSC EV-treated pigs exhibited improved outcomes, including increased exploratory behavior and faster restoration of spatiotemporal gait parameters.

conclusionsThis study demonstrated for the first time that in a large animal model novel NSC EVs significantly improved neural tissue preservation and functional levels post-MCAO, suggesting NSC EVs may be a paradigm changing stroke therapeutic.

Indexed as

Neural Stem CellsRecovery of FunctionAnimalsAnisotropyBehavior, AnimalBrainBrain EdemaBrain IschemiaCorpus CallosumDiffusion Magnetic Resonance ImagingDisease Models, AnimalExploratory BehaviorExtracellular VesiclesGaitHumansInfarction, Middle Cerebral Arterybrain ischemiaextracellular vesiclesmagnetic resonance imagingstrokewhite matter

Identifiers

PMID29650593
PMCPMC5916046
OpenAlexW2796652469

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.