Independent helper virus packaging cell line for propagating...

Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S354000, C435S366000, C435S320100, C536S023100, C536S024500

Reexamination Certificate

active

07439060

ABSTRACT:
Provided are novel vectors and viral vectors capable of expressing exogenous gene or exogenous nucleic acid sequences in a target cell of interest, such as T cells, bone marrow cells, epithelial cells, liver cells and the like. The nucleic acid components of the vectors may include one or more native promoter/enhancer regions having modified sequence segments, one or more non-native promoter/enhancer or non-native promoter's gene or gene segment, and a native viral vector terminator or processing signal or segment thereof. The viral vectors comprise a virus or viral portion having on the surfaces or envelopes adsorption components, one for a packaging cell line and the other for delivery to a target cell. Packaging cell lines for propagating the vectors and viral vectors are also provided, as are novel processes for propagating any of the disclosed vectors or viral vectors.

REFERENCES:
patent: 5166320 (1992-11-01), Wu et al.
patent: 5278056 (1994-01-01), Bank et al.
patent: 5474935 (1995-12-01), Chatterjee et al.
patent: 5650309 (1997-07-01), Wong-Staal et al.
patent: 5658776 (1997-08-01), Flotte et al.
patent: 5681746 (1997-10-01), Bodner et al.
patent: 5686279 (1997-11-01), Finer et al.
patent: 5814500 (1998-09-01), Dietz
patent: 5856152 (1999-01-01), Wilson et al.
patent: 6013517 (2000-01-01), Respess et al.
patent: 6156497 (2000-12-01), Kaleko et al.
patent: 6271348 (2001-08-01), Bujard et al.
patent: 128332 (1995-08-01), None
patent: 07793652 (1997-06-01), None
patent: WO 9506743 (1995-03-01), None
patent: WO 9613598 (1996-05-01), None
patent: WO 9636705 (1996-11-01), None
patent: WO9837917 (1998-09-01), None
Salmons et al., Human Gene Therapy, vol. 4, pp. 129-141, 1993.
Alan E. Smith, Annu. Rev. Microbiol., vol. 49, pp. 807-838, 1995.
Strair et al., Nucleic Acids Res., 1993, vol. 21, No. 20, pp. 4836-4842.
Morgenstern, J.P. et al, “Choice and Manipulation of Retroviral Vectors,”Gene Transfer and Expression Protocols. Methods in Molecular Biology, vol. 7:181-193; (1991), Murray, E.J., Ed., The Humana Press, New Jersey.
Anderson, W.F, “Human Gene Therapy,”Science 256:808-813 (1992).
Mulligan, R.C, “The Basic Science of Gene Therapy,”Science 260:926-932(1993).
Smith, A.E, “Viral Vectors in Gene Therapy,”Ann Rev. Microbiol, 49:807-38(1995).
Muzyczka, N, “Use of Adeno-Associated Virus as a General Transduction Vector for Mammalian Cells,”Current Topics in Microbiolgy and Immunolgy 158:97-129.
Kotin, R.M, “Prospects for the Use of Adeno-Associated Virus as a Vector for Human Gene Therapy,”Human Gene Therapy 5:793-801 (1994).
Emerman, M et al., “Genes with Promoters in Retrovirus Vectors Can Be Independently Suppressed by an Epigenetic Mechanism,”Cell 39:459-467 (1984).
Emerman, M et al., “Quantitative Analysis of Gene Suprression in Integrated Retrovirus Vectors,”Molecular and Cellular Biology 6(1):792-800 (1986).
Yu, S.F et al., “Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells,”Proc. Natl. Acad. Sci. USA 83:3194-3198 (1986).
Hawley, R.G. et al., “Handicapped retroviral vectors efficiently transduce foreign genes into hematopoietic stem cells,”Proc. Natl. Acad. Sci. USA 84; 2406-2410 (1987).
Yee, J.K et al., “Gene expression from transcriptionally disabled retroviral vectors,”Proc. Natl. Acad. Sci. USA 84:5197-5201 (1987).
Dougherty, J.P and Temin H.M., “A promoterless retroviral vector indicates that there are sequences in U3 required for 3′ RNA processing,”Proc. Natl. Acad. Sci. USA 84:1197-1201 (1987).
Whitcomb, J.M and Hughes, S.H., “Retroviral Reverse Transcription and integration: Progress and Problems”Ann. Rev. Cell Biol. 8:275-306 (1992).
Jaenisch, R et al., “Germline Integration of Moloney Murine Leukemia Virus at the Mov13 Locus Leads to Recessive Lethal Mutation and Early Embryonic Death,”Cell 32:209-216 (1983).
Fung, Y.T. et al., “On the mechanism of retrovirus-induced avin lymphoid leucosis: Deletion and integration of the proviruses,”Proc. Natl. Acad, Sci. USA 78(6):3418-3422 (1981).
Neel, B.G. and Hayward W.S., “Avian Leukosis Virus-Induced Tumors Have Common Proviral Integration Sites and Synthesize Discrete New RNAs: Oncogenesis by Promoter Insertion,”Cell 23:323-334 (1981).
Payne, G.S. et al., “Analysis of Avian Leukosis Virus DNA and RNA in Bursal Tumors: Viral Gene Expression is Not Required for Maintenance of the Tumor Stae,”Cell 23:311-322 (1983).
Samulski, R.J et al., “Targeted integration of adeno-associated virus (AAV) into human chromosome 19,”The EMBO Journal 10(12):3941-3950 (1991).
Kotin, R.M et al., “Mapping and Direct Visualization of a Region-Specific Viral DNA Integration Site on Chromosome 19q13-qter,”Genomics 10:831-834 (1991).
Kotin et al., “Site-specific integration by adeno-associated virus,”Proc. Natl. Acad. Sci. USA 87:2211-2215 (1990).
Manser, T. and Gesteland R.F., “Human U1 Loci: Genes for Human U1 RNA Have Dramatically Similar Genomic Envrionments.”Cell 29:257-264 (1982).
Wells S. et al., “The presence of an autologous marrow stromal cell layer increases glucocerebrosidase gene transduction of long-term culture initiating cells (LTCICs) from the bone marrow of a patient with Gaucher disease,”Gene Therapy 2:512-520 (1995).
Bertolini F. et al., “Engineered Stromal Layers and Continuous Flow Culture Enhance Multidrug Resistance Gene Transfer in Hematopoietic Progenitors,”Cancer Research 56:2566-2572 (1996).
Xu L.C. et al., “Growth Factors and Stromal Support Generate Very Efficient Retroviral Transduction of Peripheral Blood CD34+Cells From Gaucher Patients.”Blood, 86(1):141-146 (1995).
Nolta J.A. et al., “Analysis of Optimal Conditions for Retroviral-Medicated Transduction of Primitive Human Hematopoietic Cells,”Blood 86(1):101-110 (1995).
Lever, A.M.L, “Gene therapy for HIV infection,”British Medical Bulletin, 51(1):149-166 (1995).
Wu C.H. 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.
Wagner E. et al., “Coupling of adenovirus to transferring-polysine/DNA complexes greatly enhances receptor-mediated gene delivery and expression of transfected genes.”Proc. Natl. Acad. Sci. USA 89: 6099-6103 (1992).
Ruoslahti E. et al., “Alignment of Biologically Active Domains in the Fibronectin Molecule,”The Journal of Biological Chemistry 256(14):7277-7281 (1981).
Crisitiano R.J. et al., “Hepatic gene therapy: Adenovirus enhancement of receptor-mediated gene delivery and expression in primary hepatocytes,”Proc Natl. Acad. Sci. USA 90:2122-2136.
Curiel D.T. et al., “Adenovirus enhancement of transferring-polysine-mediated gene delivery,”Proc. Natl. Acad. Sci. USA 88:8850-8854 (1991).
Wagner E. et al., “Influenza virus hemagglutinin HA-2 N-terminal fusogenic peptides augment gene transfer by transferring-polysine-DNA complexes: Toward a synthetic virus-like gene-transfer vehicle,”Proc. Natl. Acad. Sci. USA 89:7934-7938 (1992).
Zieve, G.W and Sauterer R.A., “Cell Biology of the snRNP Particles,”Biochemistry and Molecular Biology 25(1):1-46 (1990).
Argos P. et al., “The integrase family of site-specific recombinases: regional similarities and global diversity,”The EMBO Journal 5(2):433-440 (1986).
Sattentau, Q.J. and Weiss, R.A., “The CD4 Antigen: Physiological Ligand and HIV Receptor,”Cell 52:631-633 (1988).
Craigle, R. et al.,Cell 62:829-837 (1990).
Liu, D. et al., “Stable Human Immunodeficiency Virus Type 1 (HIV-1) Resistance in Transformed CD4+Monocytic Cells Treated with Multitargeting HIV-1 Antisense Sequences Incorporated into U1 snRNA,”Journal of Virology71(5):4079-4085 (1997).
Berkner,

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

Independent helper virus packaging cell line for propagating... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Independent helper virus packaging cell line for propagating..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Independent helper virus packaging cell line for propagating... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3995922

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