US2002192826A1PendingUtilityA1
Recombinant AAV vector-based transduction system and use of same
Priority: Mar 6, 1996Filed: Aug 12, 2002Published: Dec 19, 2002
Est. expiryMar 6, 2016(expired)· nominal 20-yr term from priority
A61P 7/00A61P 43/00A61P 37/00A61P 37/04A61P 25/16A61P 31/00A61P 31/18C12N 15/86A61P 35/00C12N 2750/14143
46
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Claims
Abstract
The present invention relates to a transduction system, comprising (a) a rep-negative AAV vector containing a foreign DNA and (b) a product providing an AAV Rep protein. The invention also relates to the use of the transduction system.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A transduction system comprising:
(a) a rep-negative AAV vector containing a foreign DNA; and (b) a product providing an AAV Rep protein.
2 . The transduction system according to claim 1 , wherein the rep-negative AAV vector is present as DNA.
3 . The transduction system according to claim 1 , wherein the foreign DNA is expressible.
4 . The transduction system according to claim 3 , wherein the foreign DNA is controlled by an inducible promoter.
5 . The transduction system according to claim 1 , wherein the product is an expressible rep-DNA.
6 . The transduction system according to claim 5 , wherein the rep-DNA is controlled by an inducible promoter.
7 . The transduction system according to claims 5 or 6 , wherein the rep-DNA is provided within the genome of an AAV virus particle.
8 . The transduction system according to claim 7 , wherein the genome contains a defective cap gene or a deleted cap gene.
9 . The transduction system according to claim 7 , wherein the genome contains at least one defective ITR sequence.
10 . The transduction system according to claim 1 , wherein the product is an AAV Rep protein.
11 . The transduction system according to claim 1 , wherein the AAV vector is connected with the product.
12 . A method for transducting cells comprising the step of introducing a tranduction system into the cells according to claim 1 .
13 . The method of claim 11 , wherein the cells are determined for gene therapy.
14 . The method of claim 11 , wherein the cells are healthy, diseased or tumor cells.
15 . The method of claim 11 , wherein the cells are present in an organism.
16 . The method of claim 11 , wherein the cells are located outside an organism.Join the waitlist — get patent alerts
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