Melanoma antigen peptide analogues
Some embodiments relate to analogs of peptides corresponding to class I MHC-restricted T cell epitopes and methods for their generation. These analogs can contain amino acid substitutions at residues that directly interact with MHC molecules, and can confer improved, modified or useful immunologic properties. Additionally, classes of analogs, in which the various substitutions comprise the non-standard residues norleucine and/or norvaline, are disclosed.
1. An isolated peptide analogue of an immunogenic peptide expressed by a pSEM plasmid consisting essentially of the sequence:
E{A, L, Nva, Nle}AGIGILT{V,
(SEQ ID NO:91)
Nva, Nle};
or
Y{M, V, Nva, Nle}DGTMSQ{V, Nva,
(SEQ ID NO:92)
Nle};
and wherein the sequence is not E{A, L}AGIGILTV (SEQ ID NO: 93) or YMDGTMSQV (SEQ ID NO: 94).
2. The isolated peptide analogue of claim 1 , wherein said peptide analogue is selected from the group consisting of ELAGIGILTNva (SEQ ID NO: 95), ENvaAGIGILTV (SEQ ID NO: 96), YVDGTMSQNva (SEQ ID NO: 97), YVDGTMSQV (SEQ ID NO: 98) and YMDGTMSQNva (SEQ ID NO: 99).
3. The isolated peptide analogue of claim 2 , consisting essentially of the amino acid sequence ENvaAGIGILTV (SEQ ID NO: 96).
4. The isolated peptide analogue of claim 2 , consisting essentially of the sequence yMdgtmsqNva (SEQ ID NO: 99).
5. An isolated peptide analogue comprising a substitution in at least one position, wherein the at least one position is at amino acid position 2 or 10, in the sequence EAAGIGILTV (SEQ ID NO: 100) having an affinity for a class I MHC binding cleft that is similar to or greater than the affinity of EAAGIGILTV (SEQ ID NO: 100) for said class I MHC binding cleft.
6. The isolated peptide of claim 5 , wherein the halftime of dissociation is similar to or greater than the halftime of dissociation of EAAGIGILTV (SEQ ID NO: 100) from said class I MHC binding cleft.
7. The isolated peptide of claim 5 , that is recognized by T cells with specificity for the peptide EAAGIGILTV (SEQ ID NO: 100).
8. An isolated peptide analogue comprising a substitution in at least one position, wherein the at least one position is at amino acid position 2 or 9, in the sequence YMDGTMSQV (SEQ ID NO: 94) having an affinity for a class I MHC binding cleft that is similar to or greater than the affinity of YMDGTMSOV (SEQ ID NO: 94) for said class I MHC binding cleft.
9. The isolated peptide of claim 8 , wherein the halftime of dissociation is similar to or greater than the halftime of dissociation of YMDGTMSQV (SEQ ID NO: 94) from said class I MHC binding cleft.
10. The isolated peptide of claim 8 , that is recognized by T cells with specificity for the peptide YMDGTMSOV (SEQ ID NO: 94).
11. A class I MHC/peptide complex, wherein the peptide has the sequence of the peptide of claim 1 .
12. The class I MHC/peptide complex of claim 11 , wherein the class I MHC/complex is an HLA-A2/Tyrosinase369-377 complex.
13. A polypeptide comprising the peptide sequence of claim 1 embedded within a liberation sequence.
14. An composition comprising any of the peptide analogues of claim 1 .
15. A nucleic acid encoding the polypeptide of claim 13 .
16. An composition comprising the nucleic acid of claim 15 .
17. A method of inducing, maintaining, or amplifying a CTL response in a mammal comprising intranodal administration of the composition of claim 14 .
18. A method of entraining a class I MHC-restricted T cell response in a mammal comprising intranodal administration of the composition of claim 14 and an immunopotentiating agent.
19. A method of inducing, maintaining, or entraining a CTL response in a mammal comprising intranodal administration of the composition of claim 16 .
20. An isolated peptide analogue of an immunogenic peptide expressed by a pSEM plasmid consisting of the following:
(a) E{A, L, Nva, Nle}AGIGILT{V, Nva, Nle} (SEQ ID NO: 91), wherein the sequence is not E{A, L}AGIGILTV (SEQ ID NO: 93); or
(b) Y{M, V, Nva, Nle}DGTMSQ{V, Nva, Nle} (SEQ ID NO: 92), wherein the sequence is not YMDGTMSQV (SEQ ID NO: 94); or
(c) either of (a) or (b) further consisting of an N-terminal extension, a C-terminal extension, or both.
21. An isolated peptide analogue of an immunogenic peptide expressed by a pSEM plasmid comprising the sequence:
E{A, L, Nva, Nle}AGJGILT{V, Nva, Nle} (SEQ ID NO: 91); or
Y{M, V, Nva, Nle}DGTMSQ{V, Nva, Nle} (SEQ ID NO: 92);
and wherein the sequence is not E{A, L}AGIGILTV (SEQ ID NO: 93) or YMDGTMSQV (SEQ ID NO: 94).
22. An isolated peptide consisting of the sequence P0-P1-P2-P3-P4-P5-P6-P7-P8-P9-P10-P11, in which:
P0 is X, XX, or XXX, wherein X specifies any amino acid or no amino acid; and
P1 is E; and
P2 is A, L, Nva, or Nle; and
P3 is A; and
P4 is G; and
P5 is I; and
P6 is G; and
P7 is I; and
P8 is L; and
P9 is T; and
[[PΩat ]]P10 is V, Nva, or Nle; and
[[PΩ+1]]P11 is X, XX, or XXX, wherein X specifies any amino acid or no amino acid; and
wherein the sequence does not comprise E{A, L}AGIGILTV (SEQ ID NO: 93).
23. An isolated peptide consisting of the sequence P0-P1-P2-P3-P4-P5-P6-P7-P8-P9-P10, in which:
P0 is X, XX, or XXX, wherein X specifies any amino acid or no amino acid; and
P1 is Y; and
P2 is M, V, Nva, or Nie; and
P3 is D; and
P4 is G; and
P5 is T; and
P6 is M; and
P7 is 5; and
P8 is Q; and
[[PΩat P9]]is V, Nva, or Nle; and
[[PΩ+1]]P10 is X, XX, or XXX, wherein X specifies any amino acid or no amino acid; and
and wherein the sequence does not comprise YMDGTMSQV (SEQ ID NO: 94).