Key result
Recombinant adeno-associated virus (rAAV) vectors provide a versatile and safe delivery platform for advancing therapeutic approaches including gene replacement, RNA interference, and CRISPR/Cas9 genome editing.
rAAV vectors provide a safe and versatile delivery platform for advancing gene replacement, knockdown, and editing therapies.
Cautions against premature adoption in cardiovascular gene therapy; leaves open validation through prospective clinical trials.
The use of recombinant adeno-associated viruses (rAAVs) ushered in a new millennium of gene transfer for therapeutic treatment of a number of conditions, including congenital blindness, hemophilia, and spinal muscular atrophy. rAAV vectors have remarkable staying power from a therapeutic standpoint, withstanding several ebbs and flows. As new technologies such as clustered regularly interspaced short palindromic repeat genome editing emerge, it is now the delivery tool-the AAV vector-that is the stalwart. The long-standing safety of this vector in a multitude of clinical settings makes rAAV a selling point in the advancement of approaches for gene replacement, gene knockdown, gene editing, and genome modification/engineering. The research community is building on these advances to develop more tailored delivery approaches and to tweak the genome in new and unique ways. Intertwining these approaches with newly engineered rAAV vectors is greatly expanding the available tools to manipulate gene expression with a therapeutic intent.
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Valdmanis et al. (2017) reported a review. Recombinant adeno-associated virus (rAAV) vectors was evaluated. Recombinant adeno-associated virus (rAAV) vectors provide a versatile and safe delivery platform for advancing therapeutic approaches including gene replacement, RNA interference, and CRISPR/Cas9 genome editing.
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