Evidence map›Paper›PMID 42082637›Full record

ArticleGene therapy2026

Clinical response to systemic AAV gene therapy in a large animal model of late-stage lysosomal storage disease.

Jacqueline E Hunter, Caitlyn M Molony, Dana L Clarke, Wojciech Panek, Charles H Vite, Sanjeev Chawla, Harish Poptani, John H Wolfe

Abstract read
In one paragraph

Article in Gene therapy, 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

8 authors.

Jacqueline E HunterResearch Institute of Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID 0000-0002-1373-2118
Caitlyn M MolonyW.F. Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Dana L ClarkeW.F. Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Wojciech PanekW.F. Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Charles H ViteW.F. Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Sanjeev ChawlaDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Harish PoptaniDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
John H WolfeResearch Institute of Children's Hospital of Philadelphia, Philadelphia, PA, USA. jhwolfe@vet.upenn.edu.ORCID 0000-0002-7497-3943

Funding

Gene transfer &NMR studies in alpha-mannosidosis brainR01DK063973 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI WOLFE, JOHN H · 2002 to 2025
$11.0M
Referral Ctr-Animal models of human genetic diseaseP40OD010939 · OD · UNIVERSITY OF PENNSYLVANIA · PI CASAL, MARGRET L · 2012 to 2023
$7.9M
Translational studies on cerebrospinal fluid (CSF)-directed gene therapy for global neurometabolic brain diseaseR01NS110349 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI WOLFE, JOHN H · 2019 to 2023
$3.3M
NIDDK NIH HHS R01 DK063973NIH HHS P40 OD010939NINDS NIH HHS R01 NS110349U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) R01-DK063973U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01-NS110349U.S. Department of Health & Human Services | NIH | NIH Office of the Director (OD) R01-DK063973
6 · The paper itself

Abstract

The benefit of early diagnosis and treatment has been demonstrated in animal models of several lysosomal storage diseases. In a clinical setting, however, diagnoses are often not made until after patients become symptomatic. The lysosomal storage disease alpha-mannosidosis is caused by a genetic deficiency of lysosomal alpha-mannosidase, leading to the widespread presence of storage lesions throughout the brain and other tissues. In a feline model of alpha-mannosidosis, we previously demonstrated complete correction of the brain following delivery of AAVhu.32-fMANB via the carotid artery in the early symptomatic stage. Here, we investigate the efficacy of AAV gene therapy on globally distributed storage lesions in animals with advanced disease. Some improvements in clinical parameters were observed, however these improvements were less than in animals with less advanced disease. Although the treated animals were improved compared to untreated animals, increasing the vector dose did not further improve clinical outcomes. These results further demonstrate the importance of early detection and treatment of a lysosomal storage disease to successful outcomes. Despite this, partial correction extended the lifespan of diseased cats and may be medically beneficial to patients by slowing or stabilizing the progressive degenerative course of disease.

Indexed as

alpha-MannosidosisDependovirusGenetic TherapyLysosomal Storage Diseasesalpha-MannosidaseAnimalsBrainCatsDisease Models, AnimalGene Therapy AgentsGenetic VectorsHumansalpha-Mannosidase

Identifiers

PMID42082637
PMCPMC13472877

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.