Hybrid adenovirus-AAV vector and methods of use therefor

Chemistry: molecular biology and microbiology – Treatment of micro-organisms or enzymes with electrical or... – Modification of viruses

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

4353201, 435369, C12N 1510, C12N 1564, C12N 1586

Patent

active

058561528

ABSTRACT:
The present invention provides a hybrid vector construct which comprises a portion of an adenovirus, 5' and 3' ITR sequences from an AAV, and a selected transgene. Other hybrid vectors form a polycation conjugate and incorporate an AAV rep gene in a single particle. These hybrid virus vectors are characterized by high titer transgene delivery to a host cell and the ability to stably integrate the transgene into the host cell chromosome. Also disclosed is the use of the hybrid vectors to produce large quantities of recombinant AAV.

REFERENCES:
patent: 5166320 (1992-11-01), Wu et al.
patent: 5240846 (1993-08-01), Collins et al.
patent: 5252479 (1993-10-01), Srivastava
patent: 5622856 (1997-04-01), Natsoulis
Orkin et al. "Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy" Dec. 1995.
U. S. Patent Application No. 08/331,381, filed Oct. 28, 1994.
M. Kaplitt et al, "Long-term Gene Expression and Phenotypic Correction Using Adeno-associated Virus Vectors in the Mammalian Brain", Nat. Genet., 8:148-154 (Oct., 1994).
D. Russell et al, "Adeno-associated Virus Vectors Preferentially Transduce Cells in S Phase", Proc. Natl. Acad. Sci. USA, 91:8915-8919 (Sep., 1994).
Y. Watanabe, "Serial Inbreeding of Rabbits with Hereditary Hyperlipidemia (WHHL-Rabbit)", Atherosclerosis, 36:261-268 (1980).
K. Tanzawa et al, "WHHL-Rabbit: A Low Density Lipoprotein Receptor-Deficient Animal Model for Familial Hypercholesterolemia", FEBS Letters, 118(1):81-84 (Aug., 1980).
J. Goldstein et al, "Defective Lipoprotein Receptors and Atherosclerosis--Lessons from an Animal Counterpart of Familial Hypercholesterolemia", New Engl. J. Med., 309(5):288-296 (Aug. 4, 1983).
S. Ishibashi et al, "Hypercholesterolemia in Low Density Lipoprotein Receptor Knockout Mice and its Reversal by Adenovirus-mediated Gene
S. Ishibashi et al, "Massive Xanthomatosis and Atherosclerosis in Cholesterol-fed Low Density Lipoprotein Receptor-negative Mice", J. Clin.
J. Wilson, "Cystic Fibrosis--Vehicles for Gene Therapy", Nature,
M. Horwitz, "Adenoviridae and Their Replication", 2d edition, ed. B. N. Fields, Raven Press, Ltd., New york, Chapter 60, pp. 1679-1721 (1990).
Y. Yang et al, "Cellular Immunity to Viral Antigens Limits E1-deleted Adenoviruses for Gene Therapy", Proc. Natl. Acad. Sci. USA, 91:4407-4411 (May, 1994).
J. Wilson et al, "Correction of the Genetic Defect in Hepatocytes from the Watanabe Heritable Hyperlipidemic Rabbit", Proc. Natl. Acad. Sci. USA,
J. Wilson et al, "Research Article--Transplantation of Allogenic Hepatocytes into LDL Receptor Deficient Rabbits Leads to Transient Improvement in Hypercholesterolemia", Clin. Bio., 3:21-26 (Spring, 1991)
M. Grossman et al, "Towards Liver-Directed Gene Therapy: Retrovirus-Mediated Gene Transfer into Human Hepatocytes", Som. Cell. and Mol. Gen., 17(6):601-607 (Nov., 1991).
M. Boshart et al, "A Very Strong Enhancer is Located Upstream of an Immediate Early Gene of Human Cytomegalovirus", Cell, 41:521-530 (Jun., 1985).
C. Wu et al, "Targeting Genes: Delivery and Persistent Expression of a Foreign Gene Driven by Mammalian Regulatory Elements in vivo", J. Biol. Chem., 264(29):16985-16987 (Oct. 15, 1989).
K. Fisher et al, "Biochemical and Functional Analysis of an Adenovirus-Based Ligand Complex for Gene Transfer", Biochem. J., 299:49-58 (Apr. 1, 1994).
K. Kozarsky et al, "In Vivo Correction of Low-Density Lipoprotein Receptor Deficiency in the Watanabe Heritable Hyperlipidemic Rabbit with Recombinant Adenodviruses", J. Biol. Chem., 269(18):13695-13702 (May 6, 1994).
C. Laughlin et al, "Cloning of Infectious Adeno-associated Virus Genomes in Bacterial Plasmids", Gene, 23:65-73 (Jul., 1983).
J. Price et al, "Lineage Analysis in the Vertebrate Nervous System by Retrovirus-mediated Gene Transfer", Proc. Natl. Acad. Sci. USA, 84:156-160 (Jan., 1987).
J. Wilson et al, "A Novel Mechanism for Acheiving Transgene Persistence in vivo after Somatic Gene Transfer into Hepatocytes", J. Biol. Chem.,
T. Kost et al, "The Nucleotide Sequence of the Chick Cytoplasmic beta-actin Gene", Nucl. Acids Res., 11(23):8287-8301 (Dec. 11, 1983).
J. Schreiber et al, "Recombinant Retroviruses Containing Novel Reporter Genes", BioTechniques, 14(5):818-823 (May, 1993).
J. Riordan et al, "Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA", Science, 245:1066-1073 (Sep. 8, 1989).
M. Brown et al, "A Recceptor-Mediated Pathway for Cholesterol Homeostasis", Science, 232:34-46 (Apr. 4, 1986).
T. Yamamoto et al, "The Human LDL Receptor: A Cysteine-Rich Protein with Multiple Alu Sequences in its mRNA", Cell, 39:27-38 (Nov., 1984).
R. Samulski et al, "Helper-Free Stocks of Recombinant Adeno-Associated Viruses: Normal Integration does not Require Viral Gene Expression", J. Virol., 63(9):3822-3828 (Sep., 1989).
T. Shenk et al, "Genetic Analysis of Adenoviruses" Current Topics in Microbiol. and Immunol., 111:1-39 (1984).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Hybrid adenovirus-AAV vector and methods of use therefor does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Hybrid adenovirus-AAV vector and methods of use therefor, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Hybrid adenovirus-AAV vector and methods of use therefor will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-861371

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.