Evidence map›Paper›PMID 42420476›Full record

ArticleNature biotechnology2026

Efficient targeting of human glial progenitor cells in vivo with engineered AAV vectors and glymphatic delivery.

Alexander Cona, Evan Newbold, Deniz Kesmen, Rajiv Snape, Jessica Danner, Nicholas White, William Borden, Abigail Iseson, Steven J Schanz, Devin Chandler-Militello and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 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

5 · Who and what money

Authors and funding

16 authors.

Alexander Cona *Center for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.ORCID http://orcid.org/0009-0009-8065-9414
Evan Newbold *Center for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Deniz KesmenCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Rajiv SnapeCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.ORCID http://orcid.org/0009-0002-2511-8665
Jessica DannerCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Nicholas WhiteCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.ORCID http://orcid.org/0009-0005-9012-7535
William BordenCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Abigail IsesonCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.ORCID http://orcid.org/0009-0009-6054-5962
Steven J SchanzCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Devin Chandler-MilitelloCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Xiaojie LiCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Jose C CanoCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
John N MarianiCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Maiken NedergaardCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Abdellatif BenraissCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Steven A GoldmanCenter for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA. steven_goldman@urmc.rochester.edu.ORCID http://orcid.org/0000-0002-5498-4303

Funding

The glymphatic system at the crossroad of integrative health approaches inchronic painR01AT011439 · NCCIH · UNIVERSITY OF ROCHESTER · PI NEDERGAARD, MAIKEN · 2021 to 2025
$3.1M
Disruption of restorative processes in chronic stress: An integrated cellular approachR01AT012707 · NCCIH · UNIVERSITY OF WISCONSIN-MADISON · PI Chiara Cirelli, Maiken Nedergaard · 2024 to 2026
$2.0M
TRANSCRIPTIONAL DETERMINANTS OF THE FATE TRAJECTORIES OF SINGLE HUMAN GLIAL PROGENITOR CELLS IN RESPONSE TO DEMYELINATION IN VIVOR01NS110776 · NINDS · UNIVERSITY OF ROCHESTER · PI GOLDMAN, STEVEN ALAN · 2019 to 2023
$1.8M
Cell-intrinsic and contextual determinants of aging by human glial progenitor cellsR01AG072298 · NIA · UNIVERSITY OF ROCHESTER · PI GOLDMAN, STEVEN ALAN · 2021 to 2025
$1.6M
U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AG072298U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AT011439U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AT012707U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01NS110776
6 · The paper itself

Abstract

Treatment of neurological diseases that involve oligodendrocytes or astrocytes would benefit from the selective delivery of viral vectors to their common parent, glial progenitor cells (GPCs). Here, we select adeno-associated virus (AAV) capsids with tropism for human GPCs and demonstrate efficient and widespread delivery of the resultant AAVs throughout the mouse brain through the glymphatic system. In vivo screening of a library of capsid-modified, recombination-reported AAVs in chimeric mice engrafted with PDGFRA-driven Cre recombinase-expressing human GPCs identified a set of AAV5-based vectors that preferentially infect human GPCs and/or their astrocyte and oligodendrocyte progeny in vivo, with minimal systemic infection. To maximize the intracerebral distribution of these vectors while minimizing their dosing and extracerebral spread, we paired intracisternal delivery with systemic hypertonicity to increase glymphatic influx. This method bypasses the blood-brain barrier, delivering AAV directly into the brain parenchyma. Glymphatic delivery of our capsid-modified AAV5s enables efficient transgene delivery to human glia throughout the entire adult mouse brain, with minimal off-target transduction.

Identifiers

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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.