Literature DB >> 25588740

Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate rats.

J Hordeaux1, L Dubreil2, J Deniaud2, F Iacobelli2, S Moreau2, M Ledevin2, C Le Guiner3, V Blouin3, J Le Duff3, A Mendes-Madeira3, F Rolling3, Y Cherel2, P Moullier4, M-A Colle2.   

Abstract

Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in several clinical trials. However, delivery into the brain requires multiple injections and is not efficient to target the spinal cord, thus limiting its applications. To assess widespread and less invasive strategies, we tested intravenous (IV) or intrathecal (that is, in the cerebrospinal fluid (CSF)) delivery of a rAAVrh10-egfp vector in adult and neonate rats and studied the effect of the age at injection on neurotropism. IV delivery is more efficient in neonates and targets predominantly Purkinje cells of the cerebellum and sensory neurons of the spinal cord and dorsal root ganglia. A single intra-CSF administration of AAVrh10, single strand or oversized self-complementary, is efficient for the targeting of neurons in the cerebral hemispheres, cerebellum, brainstem and spinal cord. Green fluorescent protein (GFP) expression is more widespread in neonates when compared with adults. More than 50% of motor neurons express GFP in the three segments of the spinal cord in neonates and in the cervical and thoracic regions in adults. Neurons are almost exclusively transduced in neonates, whereas neurons, astrocytes and rare oligodendrocytes are targeted in adults. These results expand the possible routes of delivery of AAVrh10, a serotype that has shown efficacy and safety in clinical trials concerning neurodegenerative diseases.

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Year:  2015        PMID: 25588740     DOI: 10.1038/gt.2014.121

Source DB:  PubMed          Journal:  Gene Ther        ISSN: 0969-7128            Impact factor:   5.250


  43 in total

1.  Transduction characteristics of adeno-associated virus vectors expressing cap serotypes 7, 8, 9, and Rh10 in the mouse brain.

Authors:  Cassia N Cearley; John H Wolfe
Journal:  Mol Ther       Date:  2006-01-18       Impact factor: 11.454

2.  Expansive gene transfer in the rat CNS rapidly produces amyotrophic lateral sclerosis relevant sequelae when TDP-43 is overexpressed.

Authors:  David B Wang; Robert D Dayton; Phillip P Henning; Cooper D Cain; Li Ru Zhao; Lisa M Schrott; Elysse A Orchard; David S Knight; Ronald L Klein
Journal:  Mol Ther       Date:  2010-09-28       Impact factor: 11.454

3.  RH10 provides superior transgene expression in mice when compared with natural AAV serotypes for neonatal gene therapy.

Authors:  Chuhong Hu; Ronald W Busuttil; Gerald S Lipshutz
Journal:  J Gene Med       Date:  2010-09       Impact factor: 4.565

Review 4.  Gene therapy for lysosomal storage diseases (LSDs) in large animal models.

Authors:  Mark Haskins
Journal:  ILAR J       Date:  2009

5.  Characterization of genome integrity for oversized recombinant AAV vector.

Authors:  Biao Dong; Hiroyuki Nakai; Weidong Xiao
Journal:  Mol Ther       Date:  2009-11-10       Impact factor: 11.454

6.  Efficient intracerebral delivery of AAV5 vector encoding human ARSA in non-human primate.

Authors:  Marie-Anne Colle; Françoise Piguet; Lise Bertrand; Sylvie Raoul; Ivan Bieche; Laurence Dubreil; Didi Sloothaak; Céline Bouquet; Philippe Moullier; Patrick Aubourg; Yan Cherel; Nathalie Cartier; Caroline Sevin
Journal:  Hum Mol Genet       Date:  2010-01-01       Impact factor: 6.150

7.  Adeno-associated virus vector-mediated transduction in the cat brain.

Authors:  Charles H Vite; Marco A Passini; Mark E Haskins; John H Wolfe
Journal:  Gene Ther       Date:  2003-10       Impact factor: 5.250

8.  Whole body correction of mucopolysaccharidosis IIIA by intracerebrospinal fluid gene therapy.

Authors:  Virginia Haurigot; Sara Marcó; Albert Ribera; Miguel Garcia; Albert Ruzo; Pilar Villacampa; Eduard Ayuso; Sònia Añor; Anna Andaluz; Mercedes Pineda; Gemma García-Fructuoso; Maria Molas; Luca Maggioni; Sergio Muñoz; Sandra Motas; Jesús Ruberte; Federico Mingozzi; Martí Pumarola; Fatima Bosch
Journal:  J Clin Invest       Date:  2013-07-01       Impact factor: 14.808

9.  Widespread spinal cord transduction by intrathecal injection of rAAV delivers efficacious RNAi therapy for amyotrophic lateral sclerosis.

Authors:  Hongyan Wang; Bin Yang; Linghua Qiu; Chunxing Yang; Joshua Kramer; Qin Su; Yansu Guo; Robert H Brown; Guangping Gao; Zuoshang Xu
Journal:  Hum Mol Genet       Date:  2013-09-18       Impact factor: 6.150

10.  Adeno-associated virus of a single-polarity DNA genome is capable of transduction in vivo.

Authors:  Xiaohuai Zhou; Xinghua Zeng; Zhenghong Fan; Chengwen Li; Thomas McCown; R Jude Samulski; Xiao Xiao
Journal:  Mol Ther       Date:  2008-01-08       Impact factor: 11.454

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  24 in total

Review 1.  Viral vectors for therapy of neurologic diseases.

Authors:  Sourav R Choudhury; Eloise Hudry; Casey A Maguire; Miguel Sena-Esteves; Xandra O Breakefield; Paola Grandi
Journal:  Neuropharmacology       Date:  2016-02-21       Impact factor: 5.250

2.  Efficient CNS targeting in adult mice by intrathecal infusion of single-stranded AAV9-GFP for gene therapy of neurological disorders.

Authors:  K Bey; C Ciron; L Dubreil; J Deniaud; M Ledevin; J Cristini; V Blouin; P Aubourg; M-A Colle
Journal:  Gene Ther       Date:  2017-04-20       Impact factor: 5.250

3.  Slow Infusion of Recombinant Adeno-Associated Viruses into the Mouse Cerebrospinal Fluid Space.

Authors:  Dan Wang; Jia Li; Karen Tran; Daniel R Burt; Li Zhong; Guangping Gao
Journal:  Hum Gene Ther Methods       Date:  2018-03-29       Impact factor: 2.396

4.  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 5.  Strategies to circumvent humoral immunity to adeno-associated viral vectors.

Authors:  Longping V Tse; Sven Moller-Tank; Aravind Asokan
Journal:  Expert Opin Biol Ther       Date:  2015-06       Impact factor: 4.388

6.  Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice.

Authors:  Afrooz Rashnonejad; Gholamhossein Amini Chermahini; Cumhur Gündüz; Hüseyin Onay; Ayça Aykut; Burak Durmaz; Meral Baka; Qin Su; Guangping Gao; Ferda Özkınay
Journal:  Mol Ther       Date:  2019-08-31       Impact factor: 11.454

Review 7.  Crossing the blood-brain barrier with AAV vectors.

Authors:  Dan Liu; Mingyang Zhu; Yuqian Zhang; Yong Diao
Journal:  Metab Brain Dis       Date:  2020-11-17       Impact factor: 3.584

8.  A Single Injection of Recombinant Adeno-Associated Virus into the Lumbar Cistern Delivers Transgene Expression Throughout the Whole Spinal Cord.

Authors:  Yansu Guo; Dan Wang; Tao Qiao; Chunxing Yang; Qin Su; Guangping Gao; Zuoshang Xu
Journal:  Mol Neurobiol       Date:  2015-06-07       Impact factor: 5.590

Review 9.  Intersectional targeting of defined neural circuits by adeno-associated virus vectors.

Authors:  Chase A Weinholtz; Michael J Castle
Journal:  J Neurosci Res       Date:  2020-12-20       Impact factor: 4.164

10.  A Comprehensive Map of CNS Transduction by Eight Recombinant Adeno-associated Virus Serotypes Upon Cerebrospinal Fluid Administration in Pigs.

Authors:  Nicolina Cristina Sorrentino; Veronica Maffia; Sandra Strollo; Vincenzo Cacace; Noemi Romagnoli; Anna Manfredi; Domenico Ventrella; Francesco Dondi; Francesca Barone; Massimo Giunti; Anne-Renee Graham; Yan Huang; Susan L Kalled; Alberto Auricchio; Maria Laura Bacci; Enrico Maria Surace; Alessandro Fraldi
Journal:  Mol Ther       Date:  2015-12-07       Impact factor: 11.454

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