Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration

Preclinical studies have demonstrated that a single injection of an adeno-associated virus (AAV) vector into the cerebrospinal fluid (CSF) can achieve widespread gene transfer throughout the central nervous system. Successfully translating this approach to humans requires identifying factors that in...

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Main Authors: Christian Hinderer, Nathan Katz, Cecilia Dyer, Tamara Goode, Julia Johansson, Peter Bell, Laura Richman, Elizabeth Buza, James M. Wilson
Format: Article
Language:English
Published: Elsevier 2020-06-01
Series:Molecular Therapy: Methods & Clinical Development
Subjects:
AAV
Online Access:http://www.sciencedirect.com/science/article/pii/S2329050120300723
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spelling doaj-8162add8381d4358846b1c4b48a124372020-11-25T03:50:11ZengElsevierMolecular Therapy: Methods & Clinical Development2329-05012020-06-0117969974Translational Feasibility of Lumbar Puncture for Intrathecal AAV AdministrationChristian Hinderer0Nathan Katz1Cecilia Dyer2Tamara Goode3Julia Johansson4Peter Bell5Laura Richman6Elizabeth Buza7James M. Wilson8Gene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USAGene Therapy Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Corresponding author: James M. Wilson, Gene Therapy Program, Perelman School of Medicine, University of Pennsylvania, 125 S. 31st Street, Suite 1200 TRL, Philadelphia, PA 19104-3403, USA.Preclinical studies have demonstrated that a single injection of an adeno-associated virus (AAV) vector into the cerebrospinal fluid (CSF) can achieve widespread gene transfer throughout the central nervous system. Successfully translating this approach to humans requires identifying factors that influence AAV distribution in the CSF so that optimal parameters can be replicated in the clinic. In the context of developing a motor neuron-targeted gene therapy for spinal muscular atrophy, we conducted studies in nonhuman primates to evaluate the impact of injection volume on spinal cord transduction after AAV delivery via lumbar puncture. Lumbar injection of an AAVhu68 vector targeted motor neurons throughout the spinal cord, but only in juvenile nonhuman primates administered large injection volumes, equivalent to about half of the total CSF volume. Upon repeating this study with clinically relevant injection volumes and larger animals, we found that lumbar puncture failed to achieve significant transduction of the spinal cord. In contrast, vector administered into the cisterna magna distributed reproducibly throughout the spinal cord in both juvenile and adult animals. These findings highlight the challenges of translating AAV delivery via lumbar puncture to humans and suggest that delivery into the cisterna magna may represent a more feasible alternative.http://www.sciencedirect.com/science/article/pii/S2329050120300723AAVcentral nervous systemintrathecalcerebrospinal fluidlumbar puncturecisterna magna
collection DOAJ
language English
format Article
sources DOAJ
author Christian Hinderer
Nathan Katz
Cecilia Dyer
Tamara Goode
Julia Johansson
Peter Bell
Laura Richman
Elizabeth Buza
James M. Wilson
spellingShingle Christian Hinderer
Nathan Katz
Cecilia Dyer
Tamara Goode
Julia Johansson
Peter Bell
Laura Richman
Elizabeth Buza
James M. Wilson
Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
Molecular Therapy: Methods & Clinical Development
AAV
central nervous system
intrathecal
cerebrospinal fluid
lumbar puncture
cisterna magna
author_facet Christian Hinderer
Nathan Katz
Cecilia Dyer
Tamara Goode
Julia Johansson
Peter Bell
Laura Richman
Elizabeth Buza
James M. Wilson
author_sort Christian Hinderer
title Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
title_short Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
title_full Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
title_fullStr Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
title_full_unstemmed Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
title_sort translational feasibility of lumbar puncture for intrathecal aav administration
publisher Elsevier
series Molecular Therapy: Methods & Clinical Development
issn 2329-0501
publishDate 2020-06-01
description Preclinical studies have demonstrated that a single injection of an adeno-associated virus (AAV) vector into the cerebrospinal fluid (CSF) can achieve widespread gene transfer throughout the central nervous system. Successfully translating this approach to humans requires identifying factors that influence AAV distribution in the CSF so that optimal parameters can be replicated in the clinic. In the context of developing a motor neuron-targeted gene therapy for spinal muscular atrophy, we conducted studies in nonhuman primates to evaluate the impact of injection volume on spinal cord transduction after AAV delivery via lumbar puncture. Lumbar injection of an AAVhu68 vector targeted motor neurons throughout the spinal cord, but only in juvenile nonhuman primates administered large injection volumes, equivalent to about half of the total CSF volume. Upon repeating this study with clinically relevant injection volumes and larger animals, we found that lumbar puncture failed to achieve significant transduction of the spinal cord. In contrast, vector administered into the cisterna magna distributed reproducibly throughout the spinal cord in both juvenile and adult animals. These findings highlight the challenges of translating AAV delivery via lumbar puncture to humans and suggest that delivery into the cisterna magna may represent a more feasible alternative.
topic AAV
central nervous system
intrathecal
cerebrospinal fluid
lumbar puncture
cisterna magna
url http://www.sciencedirect.com/science/article/pii/S2329050120300723
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