Production of recombinant adeno-associated virus vectors
AssigneeApplied Immune Sciences, Inc.
InventorsJane S. Lebkowski, Maureen A. McNally, Thomas B. Okarma
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AssigneeApplied Immune Sciences, Inc.
InventorsJane S. Lebkowski, Maureen A. McNally, Thomas B. Okarma
Estimating the term…
Simplified methods to produce recombinant adeno-associated virus (rAAV) vectors are described. The methods involve the use of chimeric plasmids which incorporate the Epstein Barr nuclear antigen (EBNA) gene, the latent origin of replication of Epstein Barr virus (oriP), and a rAAV genome. The chimeric plasmids themselves are also a part of the present invention. These plasmids are maintained as multicopy extra-chromosomal elements in cells, such as human 293 cells. Permanent cell lines carrying these EBV/AAV plasmids are induced to produce large amounts of rAAV upon addition of wild-type, adeno-associated virus helper functions. Vectors produced in this manner are capable of transducing exogenous genes into other human cell lines and exhibit the attributes of vital elements produced by conventional methods.
A method for producing a recombinant adeno-associated virus comprising the steps of:
A method for producing recombinant adeno-associated virus comprising the steps of:
A cell line comprising an AAV/EBV plasmid vector, said AAV/EBV plasmid vector comprising:
A cell line comprising an AAV/EBV plasmid vector, said AAV/EBV plasmid vector comprising:
Dependencies are inferred from the claim text.