Gene therapy 2.0: genetic therapies for non-genetic disorders in neurology

“...the potential benefits from harnessing genetic therapies for relief in a widening range of non-genetic disorders is worth a deliberate effort...” Gene therapy has largely been confined to replacing faulty genes in rare genetic disorders, but a growing body of evidence suggests genetic tools can also be used to correct abnormal neuronal activity in diseases with no genetic cause. Advances in neuroscience have yielded a broad toolkit including miRNAs, ASOs, and CRISPRa capable of precisely modulating specific circuits, with early clinical successes already demonstrated in Parkinson’s disease and epilepsy. Key challenges remain, including the invasiveness of direct brain delivery and the permanence of virally-delivered modifications, though reversible approaches such as chemogenetics and inducible systems offer a path forward.

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Publication Details

Journal
Cell and Gene Therapy Insights
Published
2026-04-29
DOI
https://doi.org/10.18609/cgti.2026.036
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
0.00
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article

Gene therapy 2.0: genetic therapies for non-genetic disorders in neurology

Stéphanie Schorge
Cell and Gene Therapy Insights
Virus-based gene therapy research
article

Gene therapy 2.0: genetic therapies for non-genetic disorders in neurology

Stéphanie Schorge
article en

Abstract

“...the potential benefits from harnessing genetic therapies for relief in a widening range of non-genetic disorders is worth a deliberate effort...” Gene therapy has largely been confined to replacing faulty genes in rare genetic disorders, but a growing body of evidence suggests genetic tools can also be used to correct abnormal neuronal activity in diseases with no genetic cause. Advances in neuroscience have yielded a broad toolkit including miRNAs, ASOs, and CRISPRa capable of precisely modulating specific circuits, with early clinical successes already demonstrated in Parkinson’s disease and epilepsy. Key challenges remain, including the invasiveness of direct brain delivery and the permanence of virally-delivered modifications, though reversible approaches such as chemogenetics and inducible systems offer a path forward.

Cell and Gene Therapy InsightsVol. 12(3)
SOAS University of London (GB), University College London (GB)
Openalex Percentile: Top 10%
Virus-based gene therapy research
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