Evidence map›Paper›PMID 40086764›Full record

ReviewBrain research bulletin2025

Advantages and challenges of using allogeneic vs. autologous sources for neuronal cell replacement in Parkinson's disease: Insights from non-human primate studies.

Marina E Emborg, Jeanette M Metzger, Kevin D'Amour, Julia C Colwell, Lindsey C Neumann, Ai Zhang, Howard J Federoff

Abstract readReview
In one paragraph

Review in Brain research bulletin, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Novel Pyrido[3,4-ACS medicinal chemistry letters · 2025
    Article
  5. 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

7 authors.

Marina E EmborgPreclinical Parkinson's Research Program, Wisconsin National Primate Research Center, University of Wisconsin-Madison, USA; Department of Medical Physics, University of Wisconsin-Madison, USA; Cellular and Molecular Pathology Graduate Program, University of Wisconsin-Madison, USA. Electronic address: emborg@primate.wisc.edu.
Jeanette M MetzgerPreclinical Parkinson's Research Program, Wisconsin National Primate Research Center, University of Wisconsin-Madison, USA.
Kevin D'AmourStemson Therapeutics, San Diego, CA, USA.
Julia C ColwellPreclinical Parkinson's Research Program, Wisconsin National Primate Research Center, University of Wisconsin-Madison, USA; Cellular and Molecular Pathology Graduate Program, University of Wisconsin-Madison, USA.
Lindsey C NeumannPreclinical Parkinson's Research Program, Wisconsin National Primate Research Center, University of Wisconsin-Madison, USA.
Ai ZhangGenentech, South San Francisco, CA, USA.
Howard J FederoffKenai Therapeutics, San Diego, CA, USA; Georgetown University Medical Center, Washington, DC, USA.

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
Frontotemporal dementia in rhesus macaquesR01NS124857 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI MARINA EMBORG · 2024 to 2026
$2.2M
Graduate Training In Cellular And Molecular Pathogenesis Of Human DiseasesT32GM081061 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FABRY, ZSUZSANNA · 2010 to 2019
$1.8M
Modeling Frontotemporal Dementia in Rhesus MacaquesR33NS115102 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CHEN, RUI, EMBORG, MARINA · 2022 to 2024
$1.8M
In vitro nonhuman primate model of frontotemporal dementiaF31AG084303 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI COLWELL, JULIA CLAIRE · 2024 to 2025
$79k
NIA NIH HHS F31 AG084303NIGMS NIH HHS T32 GM081061NIH HHS P51 OD011106NINDS NIH HHS R01 NS124857NINDS NIH HHS R33 NS115102
6 · The paper itself

Abstract

Intracerebral grafting of dopamine-producing cells is proposed as a strategy to replace the typical neurons lost to Parkinson's disease (PD) and improve PD motor symptoms. Non-human primate studies have provided clues on the relationship between the host's immune response and grafting success. Herein, we discuss how the host's immune system differentially affects the graft depending on the origin of the cells and reflect on the advantages and limitations of the immune paradigms utilized to assess graft-related outcomes. We also consider new strategies to minimize or circumvent the host's immunological response and related preclinical research needed to identify the most promising new approaches to be translated into the clinic.

Indexed as

NeuronsParkinson DiseaseAnimalsDopaminergic NeuronsHumansPrimatesTransplantation, AutologousTransplantation, HomologousAllogeneicAutologousDopamineGraftsParkinson’s diseaseStem cells

Identifiers

PMID40086764
PMCPMC12036832

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.