Claims
- 1. A cancer vaccine comprising a lipid-nucleic acid (LNA) formulation in combination with at least one tumor-associated antigen, wherein said at least one tumor-associated antigen is mixed with or associated with said LNA formulation, said LNA formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide,
wherein said vaccine is capable of stimulating a Th-1 biased immune response in vivo to said at least one tumor-associated antigen.
- 2. The vaccine according to claim 1, wherein said at least one tumor-associated antigen comprises a single epitope.
- 3. The vaccine according to claim 1, wherein said at least one tumor-associated antigen comprises a plurality of epitopes from the same antigen.
- 4. The vaccine according to claim 1, wherein said vaccine comprises a plurality of tumor-associated antigens.
- 5. The vaccine according to claim 1, wherein said tumor-associated antigen comprises a self antigen.
- 6. The vaccine according to claim 1, wherein said tumor-associated antigen is associated with said LNA formulation.
- 7. The vaccine according to claim 1, wherein said tumor-associated antigen is mixed with said LNA formulation.
- 8. The vaccine according to claim 1, wherein said at least one oligonucleotide comprises at least one CpG dinucleotide.
- 9. The vaccine according to claim 8, wherein said CpG dinucleotide comprises a methylated cytosine.
- 10. A polytope cancer vaccine comprising a lipid-nucleic acid (LNA) formulation in combination with a plurality of tumor-associated antigens, wherein said plurality of tumor-associated antigens are associated with said LNA formulation, said formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide having at least one CpG dinucleotide,
wherein said vaccine is capable of simultaneously delivering said plurality of tumor-associated antigens to antigen-presenting cells in conjunction with adjuvant immune stimulation by said CpG dinucleotide to induce a Th-1 biased immune response in vivo to said tumor-associated antigens.
- 11. The vaccine according to claim 10, wherein said at least one CpG dinucleotide comprises a methylated cytosine.
- 12. The vaccine according to claim 10, wherein at least one of said plurality of tumor-associated antigens comprises a self antigen, and said vaccine is capable of breaking immune tolerance to said self antigen.
- 13. The vaccine according to claim 10, wherein said plurality of tumor-associated antigens comprise a plurality of tumor-associated self antigens, and said vaccine is capable of breaking immune tolerance to said self antigens.
- 14. The vaccine according to claim 13, where said plurality of tumor-associated antigens comprise a plurality of tissue-specific differentiation antigens.
- 15. A method for stimulating an enhanced host immune response to a tumor comprising administering to said host a cancer vaccine comprising a lipid-nucleic acid (LNA) formulation in combination with at least one tumor-associated antigen, wherein said at least one tumor-associated antigen is mixed with or associated with said LNA formulation, said LNA formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide;
wherein said vaccine is capable of stimulating a Th-1 biased cellular immune response in vivo to said at least one tumor-associated antigen.
- 16. A method for inhibiting the growth of tumor cells in a mammalian host, comprising administering to said host a cancer vaccine comprising a lipid-nucleic acid (LNA) formulation in combination with at least one tumor-associated antigen, wherein said at least one tumor-associated antigen is mixed with or associated with said LNA formulation, said LNA formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide;
wherein said administering is effective to inhibit the growth of said tumor cells in said mammalian host.
- 17. The method according to claim 15 or 16, wherein said at least one tumor-associated antigen comprises a single epitope.
- 18. The method according to claim 15 or 16, wherein said at least one tumor-associated antigen comprises a plurality of epitopes from the same antigen.
- 19. The method according to claim 15 or 16, wherein said vaccine comprises a plurality of tumor-associated antigens.
- 20. The method according to claim 15 or 16, wherein said tumor-associated antigen comprises a self antigen.
- 21. The method according to claim 15 or 16, wherein said tumor-associated antigen is associated with said LNA formulation.
- 22. The method according to claim 15 or 16, wherein said tumor-associated antigen is mixed with said LNA formulation.
- 23. The method according to claim 15 or 16, wherein said at least one oligonucleotide comprises at least one CpG dinucleotide.
- 24. The method according to claim 23, wherein said CpG dinucleotide comprises a methylated cytosine.
- 25. The method according to claim 15 or 16, wherein said vaccine further comprises at least one microbial antigen.
- 26. A method for stimulating a host immune response to a self antigen, comprising administering to said host an immunostimulatory composition comprising a lipid-nucleic acid (LNA) formulation in combination with at least one self antigen, wherein said at least one self antigen is mixed with or associated with said LNA formulation, said LNA formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide;
wherein said administering is effective to break immune tolerance and stimulate a Th-1 biased cellular immune response against said self antigen in vivo.
- 27. A method for breaking immune tolerance to a self antigen in vivo, comprising administering to a mammalian host an immunostimulatory composition comprising a lipid-nucleic acid (LNA) formulation in combination with at least one self antigen, wherein said at least one self antigen is mixed with or associated with said LNA formulation, said LNA formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide;
wherein said administering is effective to stimulate a Th-1 biased cellular immune response against said self antigen in vivo.
- 28. The method according to claim 25 or 26, wherein said self antigen comprises a tissue-specific differentiation antigen
- 29. The method according to claim 25 or 26, wherein said self antigen is selected from the group consisting of tyrosinase, TRP1, TRP2, melanA/MART1, gp75, gp100, prostate specific antigen (PSA), prostatic acid phosphatase (PAP), prostate specific membrane antigen (PMSA), prostate stem cell antigen (PSCA), prostase, and Her2/neu.
- 30. A polytope cancer vaccine comprising a lipid-nucleic acid (LNA) formulation in combination with at least one tumor-associated antigen and at least one microbial antigen, wherein said antigens are associated with said LNA formulation, said formulation comprising:
a) a lipid component comprising at least one cationic lipid; and b) a nucleic acid component comprising at least one oligonucleotide having at least one CpG dinucleotide,
wherein said vaccine is capable of simultaneously delivering said at least one tumor-associated antigen and said at least one microbial antigen to antigen-presenting cells in conjunction with adjuvant immune stimulation by said CpG dinucleotide to induce a Th-1 biased immune response in vivo to said antigens.
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to U.S. Provisional Patent Application Serial No. 60/379,343, filed May 10, 2002; and also to U.S. Provisional Patent Application Serial No. 60/460,646 filed Apr. 4, 2003; and also to U.S. Provisional Patent Application Serial No. 60/454,298, filed Mar. 12, 2003, and also to U.S. patent application Ser. No. 09/649,527, filed Aug. 28, 2000, U.S. Provisional Application Serial No. 60/176,406, filed Jan. 13, 2000, and U.S. Provisional Patent Application Serial No. 60/151,211, filed Aug. 27, 1999; and also to U.S. patent application Ser. No. 10/290,545, filed Nov. 7, 2002, and U.S. Provisional Patent Application Serial No. 60/337,522, filed Nov. 7, 2001, the disclosures of which are expressly incorporated by reference herein.
Provisional Applications (3)
|
Number |
Date |
Country |
|
60460646 |
Apr 2003 |
US |
|
60454298 |
Mar 2003 |
US |
|
60379343 |
May 2002 |
US |