Evidence map›Paper›PMID 39059426›Full record

ArticleJournal of neurosurgery2024

Preclinical evaluation of transaxial intraputaminal trajectory for enhanced distribution of grafted cells in Parkinson's disease.

Marina E Emborg, Anthony Mancinelli, Julia C Colwell, Alexandra D Zinnen, Bruce Pape, Kevin Brunner, Viktoriya Bondarenko, Casey Fitz, Jennifer Coonen, Viktorie Menna and 10 more

Abstract read
In one paragraph

Article in Journal of neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

20 authors.

Marina E Emborg1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Anthony Mancinelli1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Julia C Colwell1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Alexandra D Zinnen1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Bruce Pape1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Kevin Brunner1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Viktoriya Bondarenko1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Casey Fitz1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Jennifer Coonen1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Viktorie Menna1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Kerri Fuchs1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Nancy Schultz-Darken1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Heather A Simmons1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.
Ha Tran4Aspen Neuroscience Inc., San Diego, California; and.
Paul Larson5Neurosurgery, Department of Medicine, University of Arizona, Tucson, Arizona.
Miles Olsen6Psychiatry, and.
Sam Hurley7Radiology, University of Wisconsin-Madison, Wisconsin.
Andres M Bratt-Leal4Aspen Neuroscience Inc., San Diego, California; and.
Edward Wirth4Aspen Neuroscience Inc., San Diego, California; and.
Jeanette M Metzger1Wisconsin National Primate Research Center, University of Wisconsin-Madison, Wisconsin.

Funding

WNPRC Supplemental Request for Nonhuman Primate Enclosures to Equip HIV/AIDS-Related Research FacilitiesP51OD011106 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI Dorota A. Grejner-Brzezinska · 2012 to 2026
$150.7M
Wisconsin Alzheimer's Disease Research CenterP30AG062715 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Barbara Brigitta Bendlin · 2019 to 2026
$34.5M
Waisman Center Intellectual and Developmental Disabilities Research CenterP50HD105353 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Brittany Gail Travers · 2021 to 2026
$8.5M
NIA NIH HHS P30 AG062715NICHD NIH HHS P50 HD105353NIH HHS P51 OD011106
6 · The paper itself

Abstract

objectiveThe objective of this study was to develop and evaluate the feasibility and safety of a novel transaxial surgical approach for the delivery of human induced pluripotent stem cell-derived dopaminergic neuroprogenitor cells (DANPCs) into the putamen nucleus using nonhuman primates and surgical techniques and tools relevant to human clinical translation.

methodsNine immunosuppressed, unlesioned adult cynomolgus macaques (4 females, 5 males) received intraputaminal injections of vehicle or DANPCs (0.9 × 105 to 1.1 × 105 cells/µL) under real-time intraoperative MRI guidance. The infusates were combined with 1-mM gadoteridol (for intraoperative MRI visualization) and delivered via two tracks per hemisphere (ventral and dorsal) using a transaxial approach. The total volumes of infusion were 25 µL and 50 µL for the right and left putamen, respectively (infusion rate 2.5 µL/min). Animals were evaluated with a battery of clinical and behavioral outcome measures and euthanized 7 or 30 days postsurgery; full necropsies were performed by a board-certified veterinary pathologist. Brain tissues were collected and processed for immunohistochemistry, including against the human-specific marker STEM121.

resultsThe optimized surgical technique and tools produced successful targeting of the putamen via the transaxial approach. Intraoperative MR images confirmed on-target intraputaminal injections in all animals. All animals survived to scheduled termination without clinical evidence of neurological deficits. The first 4 animals to undergo surgery had mild brain swelling noted at the end of surgery, of which 3 had transient reduced vision; administration of mannitol therapy and reduced intravenous fluid during the surgical procedure addressed these complications. Immunostaining against STEM121 confirmed the presence of grafted cells along the injection track within the targeted putamen area of DANPC-treated animals. All adverse histological findings were limited in scope and consistent with surgical manipulation, injection procedure, and postsurgical inflammatory response to the mechanical disruption caused by the cannula insertion.

conclusionsThe delivery system, injection procedure, and DANPCs were well tolerated in all animals. Prevention of mild brain swelling by mannitol dosing and reduction of intravenous fluids during surgery allowed visual effects to be avoided. The results of the study established that this novel transaxial approach can be used to correctly and safely target cell injections to the postcommissural putamen and support clinical investigation.

Indexed as

Macaca fascicularisPutamenAnimalsDopaminergic NeuronsFeasibility StudiesFemaleHumansInduced Pluripotent Stem CellsMagnetic Resonance ImagingMaleParkinson DiseaseStem Cell Transplantationcell transplantationfunctional neurosurgeryintraoperative MRImacaqueParkinsonputamen

Identifiers

PMID39059426
PMCPMC11609033

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.