Literature DB >> 25144894

Comparative efficacy and safety of multiple routes of direct CNS administration of adeno-associated virus gene transfer vector serotype rh.10 expressing the human arylsulfatase A cDNA to nonhuman primates.

Jonathan B Rosenberg1, Dolan Sondhi, David G Rubin, Sébastien Monette, Alvin Chen, Sara Cram, Bishnu P De, Stephen M Kaminsky, Caroline Sevin, Patrick Aubourg, Ronald G Crystal.   

Abstract

Metachromatic leukodystrophy (MLD), a fatal disorder caused by deficiency of the lysosomal enzyme arylsulfatase A (ARSA), is associated with an accumulation of sulfatides, causing widespread demyelination in both central and peripheral nervous systems. On the basis of prior studies demonstrating that adeno-associated virus AAVrh.10 can mediate widespread distribution in the CNS of a secreted lysosomal transgene, and as a prelude to human trials, we comparatively assessed the optimal CNS delivery route of an AAVrh.10 vector encoding human ARSA in a large animal model for broadest distribution of ARSA enzyme. Five routes were tested (each total dose, 1.5 × 10(12) genome copies of AAVrh.10hARSA-FLAG): (1) delivery to white matter centrum ovale; (2) deep gray matter delivery (putamen, thalamus, and caudate) plus overlying white matter; (3) convection-enhanced delivery to same deep gray matter locations; (4) lateral cerebral ventricle; and (5) intraarterial delivery with hyperosmotic mannitol to the middle cerebral artery. After 13 weeks, the distribution of ARSA activity subsequent to each of the three direct intraparenchymal administration routes was significantly higher than in phosphate-buffered saline-administered controls, but administration by the intraventricular and intraarterial routes failed to demonstrate measurable levels above controls. Immunohistochemical staining in the cortex, white matter, deep gray matter of the striatum, thalamus, choroid plexus, and spinal cord dorsal root ganglions confirmed these results. Of the five routes studied, administration to the white matter generated the broadest distribution of ARSA, with 80% of the brain displaying more than a therapeutic (10%) increase in ARSA activity above PBS controls. No significant toxicity was observed with any delivery route as measured by safety parameters, although some inflammatory changes were seen by histopathology. We conclude that AAVrh.10-mediated delivery of ARSA via CNS administration into the white matter is likely to be safe and yields the widest distribution of ARSA, making it the most suitable route of vector delivery.

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Year:  2014        PMID: 25144894      PMCID: PMC4227442          DOI: 10.1089/humc.2013.239

Source DB:  PubMed          Journal:  Hum Gene Ther Clin Dev        ISSN: 2324-8637            Impact factor:   5.032


  51 in total

1.  Morphologic study of the internalization of a lysosomal enzyme by the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells.

Authors:  M C Willingham; I H Pastan; G G Sahagian; G W Jourdian; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

2.  Kinetics of central nervous system microglial and macrophage engraftment: analysis using a transgenic bone marrow transplantation model.

Authors:  D W Kennedy; J L Abkowitz
Journal:  Blood       Date:  1997-08-01       Impact factor: 22.113

3.  Accumulation of sulfatide in neuronal and glial cells of arylsulfatase A deficient mice.

Authors:  Marie Molander-Melin; Zarah Pernber; Sebastian Franken; Volkmar Gieselmann; Jan-Eric Månsson; Pam Fredman
Journal:  J Neurocytol       Date:  2004-07

4.  Bone-marrow transplantation for metachromatic leucodystrophy.

Authors:  E Bayever; S Ladisch; M Philippart; N Brill; M Nuwer; R S Sparkes; S A Feig
Journal:  Lancet       Date:  1985-08-31       Impact factor: 79.321

5.  Lysosomal sulfatide storage in the brain of arylsulfatase A-deficient mice: cellular alterations and topographic distribution.

Authors:  D Wittke; D Hartmann; V Gieselmann; R Lüllmann-Rauch
Journal:  Acta Neuropathol       Date:  2004-08-20       Impact factor: 17.088

6.  Expression of the insulin-like growth factor-II/mannose-6-phosphate receptor in multiple human tissues during fetal life and early infancy.

Authors:  B Funk; U Kessler; W Eisenmenger; A Hansmann; H J Kolb; W Kiess
Journal:  J Clin Endocrinol Metab       Date:  1992-08       Impact factor: 5.958

Review 7.  Nerve growth factor: from animal models of cholinergic neuronal degeneration to gene therapy in Alzheimer's disease.

Authors:  Mark H Tuszynski; Armin Blesch
Journal:  Prog Brain Res       Date:  2004       Impact factor: 2.453

8.  Metachromatic leukodystrophy: consequences of sulphatide accumulation.

Authors:  V Gieselmann; S Franken; D Klein; J E Mansson; R Sandhoff; R Lüllmann Rauch; D Hartmann; V P M Saravanan; P P De Deyn; R D'Hooge; A M Van Der Linden; N Schaeren-Wiemers
Journal:  Acta Paediatr Suppl       Date:  2003-12

9.  Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells.

Authors:  Alessandra Biffi; Michele De Palma; Angelo Quattrini; Ubaldo Del Carro; Stefano Amadio; Ilaria Visigalli; Maria Sessa; Stefania Fasano; Riccardo Brambilla; Sergio Marchesini; Claudio Bordignon; Luigi Naldini
Journal:  J Clin Invest       Date:  2004-04       Impact factor: 14.808

Review 10.  Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases.

Authors:  W Krivit; J H Sung; E G Shapiro; L A Lockman
Journal:  Cell Transplant       Date:  1995 Jul-Aug       Impact factor: 4.139

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  24 in total

Review 1.  Gene therapy for metachromatic leukodystrophy.

Authors:  Jonathan B Rosenberg; Stephen M Kaminsky; Patrick Aubourg; Ronald G Crystal; Dolan Sondhi
Journal:  J Neurosci Res       Date:  2016-11       Impact factor: 4.164

2.  AAVrh.10-Mediated APOE2 Central Nervous System Gene Therapy for APOE4-Associated Alzheimer's Disease.

Authors:  Jonathan B Rosenberg; Michael G Kaplitt; Bishnu P De; Alvin Chen; Thomas Flagiello; Christiana Salami; Eduard Pey; Lingzhi Zhao; Rodolfo J Ricart Arbona; Sebastien Monette; Jonathan P Dyke; Douglas J Ballon; Stephen M Kaminsky; Dolan Sondhi; Gregory A Petsko; Steven M Paul; Ronald G Crystal
Journal:  Hum Gene Ther Clin Dev       Date:  2018-03-13       Impact factor: 5.032

Review 3.  Adeno-associated virus-based Alzheimer's disease mouse models and potential new therapeutic avenues.

Authors:  Lars M Ittner; Matthias Klugmann; Yazi D Ke
Journal:  Br J Pharmacol       Date:  2019-04-23       Impact factor: 8.739

Review 4.  Gene therapy for neurological disorders: progress and prospects.

Authors:  Benjamin E Deverman; Bernard M Ravina; Krystof S Bankiewicz; Steven M Paul; Dinah W Y Sah
Journal:  Nat Rev Drug Discov       Date:  2018-08-10       Impact factor: 84.694

5.  Mapping the Structural Determinants Required for AAVrh.10 Transport across the Blood-Brain Barrier.

Authors:  Blake H Albright; Claire M Storey; Giridhar Murlidharan; Ruth M Castellanos Rivera; Garrett E Berry; Victoria J Madigan; Aravind Asokan
Journal:  Mol Ther       Date:  2017-10-26       Impact factor: 11.454

6.  Structure of the AAVhu.37 capsid by cryoelectron microscopy.

Authors:  Jason T Kaelber; Samantha A Yost; Keith A Webber; Emre Firlar; Ye Liu; Olivier Danos; Andrew C Mercer
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2020-02-03       Impact factor: 1.056

7.  Quantitative Whole-Body Imaging of I-124-Labeled Adeno-Associated Viral Vector Biodistribution in Nonhuman Primates.

Authors:  Douglas J Ballon; Jonathan B Rosenberg; Edward K Fung; Anastasia Nikolopoulou; Paresh Kothari; Bishnu P De; Bin He; Alvin Chen; Linda A Heier; Dolan Sondhi; Stephen M Kaminsky; Paul David Mozley; John W Babich; Ronald G Crystal
Journal:  Hum Gene Ther       Date:  2020-12       Impact factor: 5.695

Review 8.  Therapeutic potential of combined viral transduction and CRISPR/Cas9 gene editing in treating neurodegenerative diseases.

Authors:  Joshua Kuruvilla; Andrew Octavian Sasmita; Anna Pick Kiong Ling
Journal:  Neurol Sci       Date:  2018-08-03       Impact factor: 3.307

9.  Glymphatic fluid transport controls paravascular clearance of AAV vectors from the brain.

Authors:  Giridhar Murlidharan; Andrew Crowther; Rebecca A Reardon; Juan Song; Aravind Asokan
Journal:  JCI Insight       Date:  2016-09-08

10.  Long-term functional correction of cystathionine β-synthase deficiency in mice by adeno-associated viral gene therapy.

Authors:  Hyung-Ok Lee; Christiana O Salami; Dolan Sondhi; Stephen M Kaminsky; Ronald G Crystal; Warren D Kruger
Journal:  J Inherit Metab Dis       Date:  2021-10-11       Impact factor: 4.750

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