The advent of AAV9 expands applications for brain and spinal cord gene delivery

Abstract

Introduction: Straightforward studies compared adeno-associated virus (AAV) serotypes to determine the most appropriate one for robust expression in the CNS. AAV9 was efficient when directly injected into the brain, but more surprisingly, AAV9 produced global expression in the brain and spinal cord after a peripheral, systemic route of administration to neonatal mice.

Areas covered: Topics include AAV9 gene delivery from intraparenchymal, intravenous, intrathecal and intrauterine routes of administration, and related preclinical studies and disease models. Systemic AAV9 gene transfer yields remarkably consistent neuronal expression, though only in early development. AAV9 is versatile to study neuropathological proteins: microtubule-associated protein tau and transactive response DNA-binding protein 43 kDa (TDP-43).

Expert opinion: AAV9 will be more widely used based on current data, although other natural serotypes and recombineered vectors may also support or improve upon wide-scale expression. A peripheral-to-central gene delivery that can affect the entire CNS without having to inject the CNS is promising for basic functional experiments, and potentially for gene therapy. Systemic or intra-cerebrospinal fluid routes of AAV9 administration should be considered for spinal muscular atrophy, lysosomal storage diseases and amyotrophic lateral sclerosis, if more neuronal expression can be achieved in adults, or if glial expression can be exploited.

Keywords::

• adeno-associated virus
• amyotrophic lateral sclerosis
• frontotemporal lobar degeneration
• gene therapy
• gene transfer
• lysosomal storage disease
• microtubule-associated protein tau
• spinal cord
• spinal muscular atrophy
• TDP-43

Acknowledgements

We are grateful to G Gao, JM Wilson and colleagues at the University of Pennsylvania Gene Therapy Center for providing the materials to make recombinant AAV9. J-C Paterna, D Knight, R Zweig, M Kiaei, Y Keflemariam and I Elnagar critiqued the manuscript.

Notes

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