Chemistry: molecular biology and microbiology – Vector – per se
Reexamination Certificate
2003-04-30
2010-12-28
Sajjadi, Fereydoun G (Department: 1633)
Chemistry: molecular biology and microbiology
Vector, per se
C435S235100, C424S093200
Reexamination Certificate
active
07858367
ABSTRACT:
A recombinant hybrid virus which includes: (a) a deleted adenovirus vector genome having the adenovirus 5′ and 3′ cis-elements for viral replication and encapsidation and a deletion in an adenovirus genomic region selected from the polymerase region and/or the preterminal protein region, wherein the deletion essentially prevents the expression of a functional polymerase and/or preterminal protein from the deleted region and the hybrid virus does not otherwise express a functional polymerase protein; and (b) a recombinant adeno-associated virus (AAV) vector genome flanked by the adenovirus vector genome sequences of (a), wherein the recombinant AAV vector genome includes an AAV packaging sequence and a heterologous nucleic acid sequence, wherein the heterologous nucleic acid sequence is flanked by 5′ and 3′ AAV inverted terminal repeats.
REFERENCES:
patent: 4501729 (1985-02-01), Boucher et al.
patent: 4968603 (1990-11-01), Slamon et al.
patent: 5399346 (1995-03-01), Anderson et al.
patent: 5521291 (1996-05-01), Curiel et al.
patent: 5712136 (1998-01-01), Wickham et al.
patent: 5770442 (1998-06-01), Wickham et al.
patent: 5858351 (1999-01-01), Podsakoff et al.
patent: 5861156 (1999-01-01), George et al.
patent: 5869248 (1999-02-01), Yuan et al.
patent: 5871982 (1999-02-01), Wilson et al.
patent: 5872005 (1999-02-01), Wang et al.
patent: 5877022 (1999-03-01), Stinchcomb et al.
patent: 5922315 (1999-07-01), Roy et al.
patent: 5962313 (1999-10-01), Podsakoff et al.
patent: 6013487 (2000-01-01), Mitchell
patent: 6083702 (2000-07-01), Mitchell et al.
patent: 6156303 (2000-12-01), Russell et al.
patent: 6251677 (2001-06-01), Wilson et al.
patent: 6258595 (2001-07-01), Gao et al.
patent: 6270996 (2001-08-01), Wilson et al.
patent: 6294370 (2001-09-01), Bogedain et al.
patent: 6329181 (2001-12-01), Xiao et al.
patent: 6329958 (2001-12-01), McLean et al.
patent: 6383794 (2002-05-01), Mountz et al.
patent: 2003/0017139 (2003-01-01), Souza et al.
patent: WO90/05142 (1990-05-01), None
patent: WO 00/11149 (2000-03-01), None
patent: WO 02/063025 (2002-08-01), None
Lieber et al. J. Virol. 73(11):9314-9324; 1999.
Samulski et al. J. Virol. 63(9):3822-3828; 1989.
Lieber et al., Integrating Adenovirus-Adeno-Associated Virus Hybrid Vectors Devoid of all Viral Genes,J. of Virology73(11):9314-9324 (Nov. 1999).
Pauley et al., Intercellular Transfer of the Virally Derived Precursor Form of Acid α-Glucosidase Corrects the Enzyme Deficiency in Inherited Cardioskelatal Myopathy Pompe Disease,Human Gene Therapy12:527-538 (Mar. 20, 2001).
Ding et al., Long-Term Efficacy after [E1 , polymerase] Adenovirus-Mediated Transfer of Human Acid-α-Glucosidase Gene into Glycogen Storage Disease Type II Knockout Mice,Human Gene Therapy12:955-965 (May 20, 2001).
Sun et al., Long-Term Correction of Glycogen Storage Disease Type II with a Hybrid Ad-AAV Vector,Molecular Therapy7(2):193-201 (Feb. 2003).
Notification of Transmittal of the International Search Report for PCT/US03/13323 dated Aug. 2, 2004.
Written Opinion for PCT/US03/13323 dated Oct. 19, 2004.
International Preliminary Examination Report corresponding to PCT App. No. PCT/US03/13323 dated Apr. 7, 2005.
Allen et al., “Improved Adeno-Associated Virus Vector Production with Transfection of a Single Helper Adenovirus Gene, E4orf6,” Mol. Ther., vol. 1, pp. 88-95 (2000).
Amalfitano et al., “Production and Characterization of Improved Adenovirus Vectors with the E1, E2b, and E3 Genes Deleted,” J. Virol., vol. 72, pp. 926-933 (1998).
Amalfitano et al., “Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-α-glucosidase,” PNAS, vol. 96, pp. 8861-8866 (1999).
Gao et al., “High-Titer Adeno-Associated Viral Vectors from a Rep/Cap Cell Line and Hybrid Shuttle Virus,” Hum. Gene Ther., vol. 9, pp. 2353-2362 (1998).
Gao et al., “Rep/Cap Gene Amplification and High-Yield Production of AAV in an A549 Cell Line Expressing Rep/Cap,” Mol. Ther., vol. 5, pp. 644-649 (2002).
He et al., “A simplified system for generating recombinant adenoviruses,” PNAS, vol. 95, pp. 2509-2514 (1998).
Hodges et al., “Multiply deleted [E1, polymerase-, and pTP-] adenovirus vector persists despite deletion of the preterminal protein,” J. Gene Med., vol. 2, pp. 250-259 (2000).
Lieber et al., “Recombinant Adenoviruses with Large Deletions Generated by Cre-Mediated Excision Exhibit Different Biological Properties Compared with First-Generation Vectors In Vitro and In Vivo,” J. Virol., vol. 70, pp. 8944-8960 (1996).
Liu et al., “Production of recombinant adeno-associated virus vectors using a packaging cell line and a hybrid recombinant adenovirus,” Gene Ther., vol. 6, pp. 293-299 (1999).
Muzyczka, N., “Use of adeno-associated virus as a general transduction vector for mammalian cells,” Current Topics in Microbiology and Immunology, vol. 158, pp. 97-129 (1992).
Sun et al., “Packaging of an AAV Vector Encoding Human Acid α-Glucosidase for Gene Therapy in Glycogen Storage Disease Type II with a Modified Hybrid Adenovirus-AAV Vector,” Mol. Ther., vol. 7, pp. 467-477 (2003).
Van Hove et al., “High-level production of recombinant human lysosomal acid a-glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe disease,” PNAS, vol. 93, pp. 65-70 (1996).
Weitzman et al., “Recruitment of wild-type and recombinant adeno-associated virus into adenovirus replication centers,” J. Virol., vol. 70, No. 3, pp. 1845-1854 (1996).
Zhang et al., “Recombinant adenovirus expressing adeno-associtated virus cap and rep proteins supports production of high-titer recombinant adeno-associated virus,” Gene Ther., vol. 8, pp. 704-712 (2001).
Allen et al., “Identification and Elimination of Replication-Competent Adeno-Associated Virus (AAV) That Can Arise by Nonhomologous Recombination during AAV Vector Production,” Journal of Virology. vol. 71, No. 9 pp. 6816-6822 (1997).
Conway et al., “High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap,” Gene Therapy. vol. 6 pp. 986-993 (1999).
Coulie et al., “A New Gene Coding for a Differentiation Antigen Recognized by Autologous Cytolytic T Lymphocytes on HLA-A2 Melanomas,” Journal of Experimental Medicine. vol. 180 pp. 35-42 (1994).
Daly et al., “Neonatal gene transfer leads to widespread correction of pathology in a murine model of lysosomal storage disease,” PNAS. vol. 96 pp. 2296-2300 (1999).
Franco et al., “Evasion of Immune Response to Introduced Human Acid α-Glucosidase by Liver-Restricted Expression in Glycogen Storage Disease Type II,” Molecular Therapy. vol. 12, No. 5 pp. 876-884 (2005).
Gorman et al., “Stable alteration of pre-mRNA splicing patterns by modified U7 small nuclear RNAs,” PNAS. vol. 95 pp. 4929-4934 (1998).
Hoefsloot et al., “Primary structure and processing of lysosomal α-glucosidase; homology with the intestinal sucrase—isomaltase complex,” The EMBO Journal. vol. 7, No. 6 pp. 1697-1704 (1988).
Inoue, N., and Russell, D.W., “Packaging Cells Based on Inducible Gene Amplification for the Production of Adeno-Associated Virus Vectors,” Journal of Virology. vol. 72, No. 9 pp. 7024-7031 (1998).
Jung et al., “Adeno-associated viral vector-mediated gene transfer results in long-term enzymatic and functional correction in multiple organs of Fabry mice,” PNAS. vol. 98, No. 5 pp. 2676-2681 (2001).
Kawakami et al., “Cloning of the gene coding for a shared human melanoma antigen recognized by autologous T cells infiltrating into tumor,” PNAS. vol. 91 pp. 3515-3519 (1994).
Kawakami et al., “Identifica
Amalfitano Andrea
Koeberl Dwight D.
Sun Baodong
Duke University
Jenkins Wilson Taylor & Hunt, P.A.
Sajjadi Fereydoun G
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