Convection-enhanced delivery of AAV2 in white matter-A novel method for gene delivery to cerebral cortex

被引:15
作者
Barua, N. U. [1 ]
Woolley, M. [1 ]
Bienemann, A. S. [1 ]
Johnson, D. [1 ]
Wyatt, M. J. [1 ]
Irving, C. [1 ]
Lewis, O. [1 ]
Castrique, E. [1 ]
Gill, S. S. [1 ]
机构
[1] Univ Bristol, AMBI Labs, Funct Neurosurg Res Grp, Bristol BS10 5NB, Avon, England
关键词
Convection-enhanced delivery; Gene therapy; Cerebral cortex; White matter; NEUROTROPHIC FACTOR; TRIAL; THERAPY; GDNF; INFUSION; BRAIN;
D O I
10.1016/j.jneumeth.2013.08.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Convection-enhanced delivery (CED) is currently under investigation for delivering therapeutic agents to subcortical targets in the brain. Direct delivery of therapies to the cerebral cortex, however, remains a significant challenge. New method: We describe a novel method of targeting adeno-associated viral vector (AAV) mediated gene therapies to specific cerebral cortical regions by performing high volume, high flow rate infusions into underlying white matter in a large animal (porcine) model. Results: Infusion volumes of up to 700 mu l at flow rates as high as 10 mu l/min were successfully performed in white matter without adverse neurological sequelae. Co-infusion of AAV2/5-GFP with 0.2% Gadolinium in artificial CSF confirmed transgene expression in the deep layers of cerebral cortex overlying the infused areas of white matter. Comparison with existing methods: AAV-mediated gene therapies have been previously targeted to the cerebral cortex by performing intrathalamic CED and exploiting axonal transport. The novel method described in this study facilitates delivery of gene therapies to specific regions of the cerebral cortex without targeting deep brain structures. Conclusions: AAV-mediated gene therapies can be targeted to specific cortical regions by performing CED into underlying white matter. This technique could be applied to the treatment of neurological disorders characterised by cerebral cortical degeneration. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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