Induction of tumor immunity by variants of folate binding protein
View Patent ↗The present invention is directed to variants of antigens comprising folate binding protein epitopes as a composition associated with providing immunity against a tumor in an individual. The variant is effective in inducing cytotoxic T-lymphocytes but preferably not to the extent that they become sensitive to silencing by elimination, such as by apoptosis, or by anergy, as in unresponsiveness.
1. A method of inducing immunity against a cancer expressing folate binding protein (SEQ ID NO:10) in an individual, the method comprising administering to the individual an effective amount of a first peptide comprising the amino acid sequence of a variant of a peptide fragment of the polypeptide of SEQ ID NO: 10, wherein the peptide is of at least 9 amino acids or up to about 30 amino acids and is selected from the group consisting of:
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein.
2. The method of claim 1 , further comprising administering a second peptide of at least 9 amino acids or up to about 30 amino acids selected from the group consisting of:
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
h) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 7 thereof by threonine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
i) a peptide comprising the amino acid sequence of SEQ ID NO:268 and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
j) a peptide comprising the amino acid sequence of SEQ ID NO:269 and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 269 as contained therein.
3. The method of claim 2 , wherein the first peptide is administered prior to the administration of the second peptide.
4. The method of claim 2 , wherein the first peptide is administered subsequent to the administration of the second peptide.
5. The method of claim 2 , wherein the first peptide is administered both prior to and subsequent to the administration of the second peptide.
6. The method of claim 2 , wherein the second peptide consists of an amino acid sequence selected from the group consisting of SEQ ID NO:268 (E39), SEQ ID NO:269 (E41), SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:8 and SEQ ID NO:271.
7. The method of claim 1 , wherein the individual is substantially susceptible to recurrence of cancer.
8. The method of claim 1 , wherein the cancer is breast cancer, ovarian cancer, endometrial cancer, colorectal cancer, lung cancer, renal cancer, melanoma, kidney cancer, prostate cancer, brain cancer, sarcomas, or a combination thereof.
9. The method of claim 1 , further comprising administering an adjuvant.
10. The method of claim 1 , further comprising administering a booster comprising one or more peptides selected from the group consisting of
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
h) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 7 thereof by threonine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
i) a peptide comprising the amino acid sequence of SEQ ID NO:268 and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
j) a peptide comprising the amino acid sequence of SEQ ID NO:269 and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 269 as contained therein.
11. The method of claim 1 , wherein the peptide is formulated for administration parenterally, topically, or as an inhalant, aerosol or spray.
12. A method for stimulating cytotoxic T-lymphocytes to folate binding protein (SEQ ID NO:10), comprising the step of contacting the cytotoxic T-lymphocytes with an effective amount of a peptide comprising the amino acid sequence of a variant of a peptide fragment of the polypeptide of SEQ ID NO: 10, wherein the peptide is of at least 9 amino acids or up to about 30 amino acids and is selected from the group consisting of:
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein.
13. The method of claim 12 , wherein the cytotoxic T-lymphocytes are located within a human.
14. The method of claim 12 , further comprising administering a peptide fragment of the polypeptide of SEQ ID NO:10, wherein said peptide fragment is of at least 9 amino acids or up to about 30 amino acids, and comprises SEQ ID NO:268.
15. A method of generating an immune response to folate binding protein (SEQ ID NO:10), comprising the step of administering to a human a pharmaceutical composition comprising an immunologically effective amount of a peptide comprising the amino acid sequence of a variant of a peptide fragment of the polypeptide of SEQ ID NO: 10, wherein the peptide is of at least 9 amino acids or up to about 30 amino acids and is selected from the group consisting of:
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein.
16. A method of inducing memory cytotoxic T-lymphocytes to folate binding protein (SEQ ID NO:10) in an individual comprising the step of administering an effective amount of a peptide comprising the amino acid sequence of a variant of a peptide fragment of the polypeptide of SEQ ID NO: 10, wherein the peptide is of at least 9 amino acids or up to about 30 amino acids and is selected from the group consisting of:
a) a peptide comprising the amino acid sequence of SEQ ID NO: 268 but for the substitution therein of amino acids at positions 5 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
b) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acid at position 5 thereof by phenylalanine, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
c) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, 6, and 7 thereof by phenylalanine, phenylalanine, alanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
d) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 6 and 7 thereof by alanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
e) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by phenylalanine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein;
f) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1, 5, and 7 thereof by phenylalanine, phenylalanine, and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein; and
g) a peptide comprising the amino acid sequence of SEQ ID NO:268 but for substitution therein of the amino acids at positions 1 and 7 thereof by glycine and threonine, respectively, and from 0 to 21 additional contiguous amino acids of SEQ ID NO: 10 that flank SEQ ID NO: 268 as contained therein.
17. The method of claim 1 , wherein the first peptide consists of an amino acid sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:8 and SEQ ID NO:271.