Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of... – Method of regulating cell metabolism or physiology
Reexamination Certificate
2005-03-15
2005-03-15
Lankford, Jr., Leon B. (Department: 1651)
Chemistry: molecular biology and microbiology
Animal cell, per se ; composition thereof; process of...
Method of regulating cell metabolism or physiology
C435S325000, C435S326000, C435S375000, C436S526000
Reexamination Certificate
active
06867041
ABSTRACT:
The present invention relates generally to methods for stimulating cells, and more particularly, to a novel method to concentrate and/or stimulate cells that maximizes stimulation and/or proliferation of such cells. In the various embodiments, cells are stimulated and concentrated with a surface yielding enhanced proliferation, cell signal transduction, and/or cell surface moiety aggregation. In certain aspects methods for stimulating a population of cells such as T-cells, by simultaneous concentration and cell surface moiety ligation are provided by contacting the population of cells with a surface, that has attached thereto one or more agents that ligate a cell surface moiety and applying a force that predominantly drives cell concentration and cell surface moiety ligation, thereby inducing cell stimulation, cell surface moiety aggregation, and/or receptor signaling enhancement. Also provided are methods for producing phenotypically tailored cells, including T-cells for the use in diagnostics, drug discovery, and the treatment of a variety of indications, including cancer, viral infection, and immune related disorders. Compositions of cells having specific phenotypic properties produced by these processes are further provided.
REFERENCES:
patent: 5190878 (1993-03-01), Wilhelm
patent: 5443983 (1995-08-01), Ochoa et al.
patent: 5470730 (1995-11-01), Greenberg et al.
patent: 5674704 (1997-10-01), Goodwin et al.
patent: 5735279 (1998-04-01), Klaveness et al.
patent: 5766944 (1998-06-01), Ruiz
patent: 5804442 (1998-09-01), Romet-Lemonne et al.
patent: 5837477 (1998-11-01), Germain et al.
patent: 5858358 (1999-01-01), June et al.
patent: 5888807 (1999-03-01), Palsson et al.
patent: 5942607 (1999-08-01), Freeman et al.
patent: 5962319 (1999-10-01), Ogawa et al.
patent: 5985653 (1999-11-01), Armstrong et al.
patent: 6096532 (2000-08-01), Armstrong et al.
patent: 6113901 (2000-09-01), Bluestone
patent: 6129916 (2000-10-01), Chang
patent: 6143297 (2000-11-01), Bluestone
patent: 6197298 (2001-03-01), Chang
patent: 6316257 (2001-11-01), Flyer et al.
patent: 6352694 (2002-03-01), June et al.
patent: 6355779 (2002-03-01), Goodwin et al.
patent: 20010031253 (2001-10-01), Gruenberg
patent: 20020090362 (2002-07-01), Strauss
patent: 20020182730 (2002-12-01), Gruenberg
patent: 20030039650 (2003-02-01), Gruenberg
patent: 20030134341 (2003-07-01), Gruenberg
patent: 20030134415 (2003-07-01), Gruenberg
patent: 20030170238 (2003-09-01), Gruenberg
patent: 20030175242 (2003-09-01), Gruenberg
patent: 20030175272 (2003-09-01), Gruenberg
patent: 20030194395 (2003-10-01), Gruenberg et al.
patent: 633930 (2000-04-01), None
patent: WO 9701304 (1997-01-01), None
patent: WO 9705233 (1997-02-01), None
patent: WO 9705239 (1997-02-01), None
patent: WO 0002520 (2000-01-01), None
patent: WO 03024312 (2003-03-01), None
patent: WO 03025158 (2003-03-01), None
patent: WO 03034820 (2003-05-01), None
patent: WO 03043643 (2003-05-01), None
patent: WO 03077658 (2003-09-01), None
Baroja, M.L. et al., “The Anti-T Cell Monoclonal Antibody 9.3 (Anti-CD28) Provides a Helper Signal and Bypasses the Need for Accessory Cells in T Cell Activation with Immobilized Anti-CD3 and Mitogens,”Cellular Immunology120: 205-217, 1989.
Bergstresser, P.R. et al., “T Cell-Mediated Terminal Maturation of Dendritic Cells,” inDendritic Cell in Fundamental and Clinical Immunology, Ricciardi-Castognoli (Ed.), Plenum Press, New York, 1997, pp. 65-69.
Groh, V. et al., “Stimulation of T cell autoreactivity by anomalous expression of NKG2D and its MIC ligands in rheumatoid arthritis,”Proceedings of the National Academy of Sciences100(16): 9452-9457, Aug. 5, 2003.
Lanzavecchia, A., “The Role of Dendritic Cells in the Generation of Effector and Memory T Cell Responses,” fromThe Midwinter Conference of Immunologists, Jan. 22-25, 2000, available at www.midwconfimmunol.org/Midwinter00/sessions/lanzavecchia.html.
Li, Q. et al., “Expanded Tumor-reactive CD4+T-Cell Responses to Human Cancers Induced by Secondary Anti-CD3/Anti-CD28 Activation,”Clinical Cancer Research5: 461-469, Feb. 1999.
Li, Q. et al., “Immunological Effects of BCG as an Adjuvant in Autologous Tumor Vaccines,”Clinical Immunology94(1): 64-72, Jan. 2000.
Zou, J.-P. et al., “Tumor-Bearing Mice Exhibit A Progressive Increase in Tumor Antigen-Presenting Cell Function and A Reciprocal Decrease in Tumor Antigen-Responsive CD4+T Cell Activity,”The Journal of Immunology148(2): 648-655, Jan. 15, 1992.
Bretscher, P., “The two-signal model of lymphocyte activation twenty-one years later,”Immunology Today13(2): 74-76, 1992.
Garland et al., “The use of Teflon cell culture bags to expand functionally active CD8+cytotoxic T lymphocytes,”Journal of Immunological Methods227: 53-63, 1999.
Haanen et al., “Selective Expansion of Cross-reactive CD8+Memory T Cells by Viral Variants,”J. Exp. Med.190(9): 1319-1328, Nov. 1, 1999.
Iezzi et al., “The Duration of Antigenic Stimulation Determines the Fate of Naive and Effector T Cells,”Immunity8: 89-95, Jan. 1998.
June et al., “The B7 and CD28 receptor families,”Immunology Today15(7): 321-331, 1994.
Kato et al., “Gene Transfer of CD40-Ligand Induces Autologous Immune Recognition of Chronic Lymphocytic Leukemia B Cells,”J. Clin. Invest.101(5): 1133-1141, Mar. 1998.
Krawczyk et al., “Cbl-b Is a Negative Regulator of Receptor Clustering and Raft Aggregation in T Cells,”Immunity13: 463-473, Oct. 2000.
Liebowitz et al., “Costimulatory approaches to adoptive immunotherapy,”Current Opinion in Oncology10: 533-541, 1998.
Ranheim and Kipps, “Activated T Cells Induce Expression of B7/BB1 on Normal or Leukemic B Cells through a CD40-dependent Signal,”J. Exp. Med.177: 925-935, Apr. 1993.
Ten Berge et al., “Selective Expansion of a Peripheral Blood CD8+Memory T Cell Subset Expressing Both Granzyme B andL-Selectin During Primary Viral Infection in Renal Allograft Recipients,”Transplantation Proceedings30: 3975-3977, 1998.
Bonyhadi, M. et al., “Xcellearate: An Autologous T Cell Immunotherapy Approach for Treating B-Cell Lymphocytic Leukemia (B-CLL),” inProceedings of the 42ndAnnual Meeting of the American Society of Hematology, San Francisco, Dec. 1-5, 2000, vol. 96, No. 11, part 1, ABSTRACT # 3616.
Creson, J. et al., “The Mode and Duration of Anti-CD28 Costimulation Determine Resistance to Infection by Macrophage-Tropic Strains of Human Immunodeficiency Virus Type 1 in Vitro,”Journal Of Virology, 73(11):9337-9347, Nov. 1999.
Hami, L. et al., “Xcellerate™: A Platform Process for the GMP Manufacture of Activated T Cells for the Treatment of Patients with Cancer and Immune Dysfunction,” inProceedings of the 42ndAnnual Meeting of the American Society of Hematology, San Francisco, Dec. 1-5, 2000, vol. 96, No. 11, part 1, abstract # 3630.
Kalamasz, D. et al., “Storage Shipment of Freshly Harvested or Cryopreserved Xcellerate™ Activated T Cells for Clinical Applications,” inProceedings of the 42ndAnnual Meeting of the American Society of Hematology, San Francisco, Dec. 1-5, 2000, vol. 96, No. 11, part 2, abstract # 5113.
Larsson, S. et al., “Productive Cytomegalovirus (CMV) Infection Exclusively in CD13-Positive Peripheral Blood Mononuclear Cells from CMV-Infected Individuals,”Transplantation, 65(3):411-415, Feb. 15, 1998.
Polanski, M. et al., “Xcellerate( : A Closed, Scalable Process for the GMP Manufacture of Stable Activated T Cells,” inProceedings of the 15thAnnual Scientific Meeting of the Society for Biological Therapy, Seattle, Oct. 26-29, 2000, andJournal of Immunotherapy, (23)5:599, Sep. 2000.
Berenson Ronald
Bonyhadi Mark
Craig Stewart
Hardwick Alan
Kalamasz Dale
Lankford , Jr. Leon B.
Seed IP Law Group PLLC
XCYTE Therapies, Inc.
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