Persistent transgene product in retina, optic nerve and brain after intraocular injection of rAAV

被引:133
作者
Dudus, L
Anand, V
Acland, GM
Chen, SJ
Wilson, JM
Fisher, KJ
Maguire, AM
Bennett, J
机构
[1] Univ Penn, Sch Med, Scheie Eye Inst, Dept Ophthalmol,Stellar Chance Labs, Philadelphia, PA 19104 USA
[2] Univ Penn, Inst Human Gene Therapy, Philadelphia, PA 19104 USA
[3] Tulane Univ, Sch Med, Dept Pathol & Lab Med, New Orleans, LA 70112 USA
[4] Cornell Univ, Coll Vet Med, James A Baker Inst Anim Hlth, Ctr Canine Genet & Reprod, Ithaca, NY 14853 USA
关键词
optic nerve tract; lateral geniculate nucleus; immune response; gene therapy; ganglion cells;
D O I
10.1016/S0042-6989(98)00308-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recombinant adeno-associated virus (rAAV) is a promising vector for retinal application as it transduces photoreceptors and retinal pigment epithelium cells efficiently and in a stable fashion. Because rAAV also transduces retinal ganglion cells, we reasoned that ocular application of rAAV might result in delivery of transgenic protein to the CNS. Here we describe high levels of green fluorescent protein (GFP) persisting at least 6 months in optic nerves and brains of mice and dogs after intravitreal delivery of rAAV-GFP. There was no clinical or histological evidence of inflammatory response although a mild humoral Th-2 response to viral capsid proteins was detected. These findings have important implications with respect to therapeutic applications of rAAV. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2545 / 2553
页数:9
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