Vaccine compositions and methods for restoring NKG2D pathway function against cancers
The present invention provides compositions and methods for treating cancer in a subject by eliciting an immune response against a MIC polypeptide.
1. A vaccine composition for treating cancer, the composition comprising
(i) as an immunogenic component, an effective amount of a peptide consisting of:
(a) amino acids 181 to 274 of SEQ ID NO: 1;
(b) SEQ ID NO: 2, 11, 12, 13, 21 or 23;
(c) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising 2, 4, 5, 6, 8, or 10 flanking amino acids on either the N-terminal end of the peptide, the C-terminal end of the peptide, or both the N-terminal end and the C-terminal end of the peptide; or
(d) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising one or more flanking amino acids such that the entire peptide consists of about 25 to 30 amino acids;
the effective amount being an amount effective to elicit an immune response against the cancer;
wherein flanking amino acids are amino acids adjacent to SEQ ID NO:11, 12, 13, 21 or 23 in SEQ ID NO: 1 or in SEQ ID NO: 14; and
(ii) an adjuvant selected from an oil-based adjuvant, a CpG DNA adjuvant, a mineral salt adjuvant, a particulate adjuvant, a mucosal adjuvant, a cytokine, a microbial derivative, an emulsion and a Toll-Like Receptor agonist.
2. The vaccine composition of claim 1 , wherein the composition is effective to elicit an in vitro immune response against a MIC polypeptide.
3. The vaccine composition of claim 1 , wherein the composition is effective to elicit an in vivo immune response against a MIC polypeptide.
4. The vaccine composition of claim 2 , wherein the MIC polypeptide is not attached to a cell.
5. The vaccine composition of claim 1 , wherein the composition is effective to elicit an immune response against a cancer cell expressing a MIC polypeptide.
6. The vaccine composition of claim 1 , wherein the MIC polypeptide is a MICA or MICB polypeptide.
7. The vaccine composition of claim 1 , wherein the cancer expresses MICA and/or MICB proteins.
8. The vaccine composition of claim 1 , wherein the cancer is melanoma.
9. The vaccine composition of claim 1 , wherein the peptide consists of SEQ ID NO: 2, 5-13, 15-21 or 23.
10. The vaccine composition of claim 1 , wherein the vaccine composition comprises a plurality of peptides consisting of:
(a) amino acids 181 to 274 of SEQ ID NO: 1;
(b) SEQ ID NO: 2, 11, 12, 13, 21 or 23;
(c) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising 2, 4, 5, 6, 8, or 10 flanking amino acids on either the N-terminal end of the peptide, the C-terminal end of the peptide, or both the N-terminal end and the C-terminal end of the peptide; or
(d) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising one or more flanking amino acids such that the entire peptide consists of about 25 to 30 amino acids.
11. The vaccine composition of claim 1 , wherein the peptide is conjugated to a carrier protein.
12. The vaccine composition of claim 11 , wherein the carrier protein is selected from tetanus toxin and diphtheria toxin.
13. The vaccine composition of claim 1 , wherein the composition comprises a viral capsid protein engineered to display the at least one peptide or plurality of peptides on its surface.
14. The vaccine composition of claim 13 , wherein the viral capsid protein is a hepatitis B capsid protein.
15. The vaccine composition of claim 1 , wherein the composition is in the form of a polymer scaffold comprising the peptide.
16. The vaccine composition of claim 15 , wherein the polymer scaffold is a porous, poly-lactide-co-glycolide (PLG) polymer scaffold.
17. The vaccine composition of claim 16 , wherein the polymer scaffold further comprises one or both of a cytokine and a Toll-like receptor agonist.
18. The vaccine composition of claim 17 , wherein the polymer scaffold further comprises autologous tumor cell lysates of a subject to be treated for cancer with the composition.
19. A method of treating cancer in a subject, the method comprising administering to a subject a vaccine composition of claim 1 .
20. The method of claim 19 , wherein the vaccine composition is administered as part of a therapeutic regimen.
21. The method of claim 20 , wherein the therapeutic regimen further comprises one or more of radiation therapy, targeted therapy, immunotherapy, or chemotherapy.
22. The method of claim 19 , wherein the vaccine composition is administered as part of a prime-boost strategy and the prime-boost strategy further comprises administering at least one, preferably two additional vaccine compositions of the invention, each vaccine composition comprising a different peptide selected from peptides consisting of:
(a) amino acids 181 to 274 of SEQ ID NO: 1;
(b) SEQ ID NO: 2, 11, 12, 13, 21 or 23;
(c) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising 2, 4, 5, 6, 8, or 10 flanking amino acids on either the N-terminal end of the peptide, the C-terminal end of the peptide, or both the N-terminal end and the C-terminal end of the peptide; or
(d) SEQ ID NO: 11, 12, 13, 21 or 23, further comprising one or more flanking amino acids such that the entire peptide consists of about 25 to 30 amino acids.
23. The vaccine composition of claim 3 , wherein the MIC polypeptide is not attached to a cell.
24. The vaccine composition of claim 1 , wherein the mineral salt adjuvant is a mineral salt gel adjuvant.
25. The vaccine composition of claim 1 , wherein the particulate adjuvant is a micro particulate adjuvant.