Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai
Reexamination Certificate
2002-03-22
2008-03-04
Yu, Misook (Department: 1642)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Peptide containing doai
Reexamination Certificate
active
07338929
ABSTRACT:
A method for stimulating a immune response against IL-13Rα2 in a subject having or at risk for developing a disease having cells expressing IL-13Rα2 includes the steps of formulating the anti-cancer vaccine outside of the subject and administering the vaccine to the subject in an amount sufficient to stimulate an immune response against IL-13Rα2 in the subject. A composition for stimulating a immune response against IL-13Rα2 in a subject having or at risk for developing a disease having cells expressing IL-13Rα2 includes an isolated agent that can stimulate immune response against IL-13α2.
REFERENCES:
patent: 5614191 (1997-03-01), Puri et al.
patent: 5710023 (1998-01-01), Collins et al.
patent: 5827703 (1998-10-01), Debs et al.
patent: 5855866 (1999-01-01), Thorpe et al.
patent: 6248714 (2001-06-01), Collins et al.
patent: 2003/0157691 (2003-08-01), Qin et al.
patent: WO 9731946 (1997-09-01), None
patent: WO 01/58479 (2001-08-01), None
patent: WO 02/097114 (2002-12-01), None
patent: WO 03/079757 (2003-10-01), None
Byers, T. (CA Journal, vol. 49, No. 6, Nov./Dec. 1999).
Bellone et al. (Immunology Today, v20 (10), 1999, pp. 457-462).
Gura (Science, v278, 1997, pp. 1041-1042).
Paine-Murrieta et al. (Cancer Chemother.Pharmacol, vol. 40, 1997, pp. 209-214).
Ben-Efraim, Tumor Biology 1999; 20: 1-24.
Marincola et al., TRENDS in Immunology 2003; 24: 334-341.
Frazer, I., Expert. Opin. Pharmacother. 2004; 5: 2427-2434.
Debinski et al., “Human Gliomas Cells Overexpress Receptors for Interleukin 13 and Are Extremely Sensitive to a Novel Chimeric Protein Composed of Interleukin 13 and Pseudomonas Exotoxin1,” Clinical Cancer Research, 1: 1253-1258, 1995.
Debinski et al., “Novel Way To Increase Targeting Specificity to a Numan Glioblastoma-Associated Receptor For Interleukin 13,” Int. J. Cancer, 76: 547-551, 1998.
Caput et al., “Cloning and Characterization of a Specific Interleukin (IL)-13 Binding Protein Structurally Related to the IL-5 Receptor α Chain,” The Journal of Biological Chemistry, 271: 16921-16926, 1996.
Debinski, W., “Recombinant Cytotoxins Specific for Cancer Cells,” Ann. NY Acad. Sci., 297-299, 1999.
Debinski et al., “Receptor for Interleukin 13 Is a Marker and Therapeutic Target for Human High-Grade Gliomas1,” Clinical Cancer Research, 5: 985-990, 1999.
Joshi et al., “Interleukin-13 Receptor α Chain: A Novel Tumor-associated Transmembrane Protein in Primary Explants of Human Malignant Gliomas,” Cancer Research, 60: 1168-1172, 2000.
Barton et al. “Retroviral delivery of small interfering RNA into primary cells”, PNAS, (2002), vol. 99, No. 23, pp. 14943-14945.
Noda et al. “Protection from Anti-TCR/CD3-Induced Apoptosis in Immature Thymocytes by a Signal Through Thymic Shared Antigen-1/Stem Cell Antigen-2”, J. Exp. Med., (1996), vol. 183, pp. 2355-2360.
Treister et al. “Expression of Ly-6, A Marker for Highly Malignant Murine Tumor Cells, is Regulated by Growth Conditions and Stress”, Int. J. Cancer, (1998), vol. 77, pp. 306-313.
McManus et al. “Gene Silencing in Mammals by Small Interfering RNAs”, Nature Reviews/Genetics, (2002), vol. 3, pp. 737-747.
Tuschl et al. “Small Interfering RNAs: A Revolutionary Tool for the Analysis of Gene Function and Gene Therapy”, Molecular Interventions, (2002), vol. 2, No. 3, pp. 158-167.
Rubinson et al. “A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA Interference”, Nature Genetics, (2003), vol. 33, pp. 401-406.
He et al. “Functional Characterization of Hepatoma-Specific Stem Cell Antigen-2”, Molecular Carcinogenesis, (2004), vol. 40, pp. 90-103.
Banerjea et al. “Inhibition of HIV-1 by Lentiviral Vector-Transduced siRNAs in T Lymphocytes Differentiated in SCID-hu Mice and CD34 Progenitor Cell-Derived Macrophages”, Molecular Therapy, (2003), vol. 8, No. 1, pp. 62-71.
Lee et al. “Inhibition of Human Immunodeficiency Virus Type 1 Replication in Primary Macrophages by Using Tat- or CCR5-Specific Small Interfering RNAs Expressed from a Lentivirus Vector”, Journal of Virology, (2003), vol. 77, No. 22, pp. 11964-11972.
Lee et al. “Expression of small interfering RNAs targeted against HIV-1 rev transcripts in human cells”, Nature Biotechnology, (2002), vol. 19, pp. 500-505.
Novina et al. “siRNA-directed inhibition of HIV-1 infection”, Nature Medicine, (2002), vol. 8, No. 7, pp. 681-686.
Coburn et al. “Potent and Specific Inhibition of Human Immunodeficiency Virus Type 1 Replication by RNA Interference”, Journal of Virology, (2002), vol. 76, No. 18, pp. 9225-9231.
Boden et al. “Promoter choice affects the potency of HIV-1 specific RNA interference”, Nucleic Acids Research, (2003), vol. 31, No. 17, pp. 5033-5038.
Pusch et al. “Nucleotide sequence homology requirements of HIV-1-specific short hairpin RNA”, Nucleic Acids Research, (2003), vol. 31, No. 22, pp. 6444-6449.
Chang et al. “Lentiviral siRNAs targeting multiple highly conserved RNA sequences of human immunodeficiency virus type 1”, Gene Therapy, (2005), vol. 12, pp. 1133-1144.
Christensen Neil
Debinski Waldemar
Mintz Akiva
Halvorson Mark
The Penn State Research Foundation
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