| Literature DB >> 30706404 |
Lakmini P Wasala1, Chady H Hakim2,3, Yongping Yue2, N Nora Yang3, Dongsheng Duan4,5,6,7,8.
Abstract
Many diseases affect multiple tissues and/or organ systems, or affect tissues that are broadly distributed. For these diseases, an effective gene therapy will require systemic delivery of the therapeutic vector to all affected locations. Adeno-associated virus (AAV) has been used as a gene therapy vector for decades in preclinical studies and human trials. These studies have shown outstanding safety and efficacy of the AAV vector for gene therapy. Recent studies have revealed yet another unique feature of the AAV vector. Specifically, AAV can lead to bodywide gene transfer following a single intravascular injection. Here we describe the protocols for effective systemic delivery of AAV in both neonatal and adult mice and dogs. We also share lessons we learned from systemic gene therapy in the murine and canine models of Duchenne muscular dystrophy.Entities:
Keywords: AAV; Adult dogs; Adult mice; DMD; Neonatal dogs; Neonatal mice; Systemic delivery
Mesh:
Year: 2019 PMID: 30706404 PMCID: PMC6690205 DOI: 10.1007/978-1-4939-9065-8_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745