Therapeutic retroviral vectors for gene therapy

Drug – bio-affecting and body treating compositions – Whole live micro-organism – cell – or virus containing – Genetically modified micro-organism – cell – or virus

Reexamination Certificate

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C435S320100, C536S024100

Reexamination Certificate

active

07901671

ABSTRACT:
The invention provides improved compositions and methods for achieving gene therapy in hematopoietic cells and hematopoietic precursor cells, including erythrocytes, erythroid progenitors, and embryonic stem cells. The invention further provides improved gene therapy methods for treating hematopoietic-related disorders. Retroviral gene therapy vectors that are optimized for erythroid specific expression and treatment of hemoglobinopathic conditions are disclosed.

REFERENCES:
patent: 5861488 (1999-01-01), LeBoulch et al.
patent: 6136597 (2000-10-01), Hope et al.
patent: 6252048 (2001-06-01), Kelley et al.
patent: 6395549 (2002-05-01), Tuan et al.
patent: 7198950 (2007-04-01), Trono et al.
patent: 2004/0241141 (2004-12-01), Pawliuk
patent: WO 94/23046 (1994-10-01), None
patent: WO 00/23606 (2000-04-01), None
patent: WO 02/082908 (2002-10-01), None
patent: WO-02/087341 (2002-11-01), None
Deonarain, M., 1998, Expert Opin. Ther. Pat., vol. 8, pp. 53-69.
Verma et al., Sep. 1997, Nature, vol. 389, pp. 239-242.
Eck et al., 1996, Goodman & Gilman's The Pharmacological Basis of Therapeutics, McGraw-Hill, New York, p. 77-101.
Gorecki, D., 2001, Expert Opin. Emerging Drugs, 6(2): 187-198.
Copreni et al., 2004, Gene Therapy, vol. 11, p. S67-S75.
Pellinen et al., 2004, International Journal of Oncology, vol. 25, p. 1753-1762.
Rudinger, 1976, Peptide Hormones, Parsons, University Park Press, Baltimore, p. 1-7.
Kaye et al., 1990, Proc. Natl. Acad. Sci. USA, vol. 87, pp. 6922-6926.
Skolnick et al., 2000, Trends in Biotech, vol. 18, p. 34-39.
LeBoulch et al., Geneseq Accession No. ABZ69006, computer printout pp. 1-3.
Bell et al., 2001, Geneseq Accession No. AAF67644, computer printout p. 5-6.
Pawliuk et al. “Correction of Sickle Cell Disease in Transgenic Mouse Models by Hematopoietic Stem Cell Gene Therapy”Blood, vol. 98, No. 11, Part 1, pp. 781a (2001).
Imren et al. “Correction of Anemia in Beta-Thalassemia Mice Transplanted with Syngeneic Marrow Transduced with Entiviral Vector Encoding Human Beta-Globin Gene”Blood, vol. 98, No. 11, Part 1, pp. 692a (2001).
Rivella et al. “Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin”Nature, 406(6791):82-86 (2000).
Pawliuk et al. “Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene Therapy”Science, 294:2368-2371 (2001).
Imren et al. “Permanent and panerythroid correction of murine β thalassemia by multiple lentiviral integration in hematopoietic stem cells”PNAS, 99(2):14380-14385 (2002).
Hino, Shinjiro et al., “Incorporation of Chromatin Insulator from Sea Urchin Arylsulfatase Gene Into Lentiviral Vector Improves Expression in Myeloid Progenitor Cells,”Gene Transfer—Biology and Marking Studies, Abstract No. 5522, p. 484b (2002).
Imren, Suzan et al., “Preferred Intragenic Integration with High-Level Erythroid Expression of a Lentiviral Vector Bearing an Anti-Sickling (β-Globin Transgene in NOD/SCID Mouse Repopulating Human Cord Blood Cells,”Gene Transfer: Biology and Marking Studies, Abstract No. 877, p. 250a (2003).
Iwakuma, Tomoo et al., “Self-Inactivating Lentiviral Vectors with U3 and U5 Modifications,”Virology, vol. 261:120-132 (1999).
Ramezani, Ali et al., “Development of Improved Lentiviral Vectors for Hemophilia A Gene Therapy,”In Vivo Gene Transfer, Abstract No. 3428, p. 869a (2002).
Yannaki, Evangelia et al., “Topological Constraints Governing the Use of the Chicken HS4 Chromatin Insulator in Oncoretrovirus Vectors,”Molecular Therapy, vol. 5(5):589-598 (2002).
Bell, A.C. et al.,“The Protein CTCF is Required for the Enhancer Blocking Activity of Vertebrate Insulators,”Cell, vol. 98:387-396 (1999).
Chung, J.H. et al.,“A 5′ Element of the Chicken β-Globin Domain Serves as an Insulator in Human Erythroid Cells and Protects against Position Effect in Drosphila,”Cell, vol. 74:505-514 (1993).
Chung, J.H. et al.,“Characterization of the chicken β-globin insulator,”Proc. Natl. Acad. Sci. USA, vol. 94:575-580 (1997).

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