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US20090041794: Identification of Hla-A2-Presented T-Cell Epitopes Derived from the Oncofoetal Antigen-Immature Laminin Receptor Protein and Uses Thereof
Filing Information
Patent Family
33 Claims, 10 Drawings
Abstract
The present invention relates to the immunotherapB of cancer, in particular several tumor entities including hematological malignancies. The present invention relates to tumor-associated T-helper cell peptide epitopes, alone or in combination with other tumor-associated peptides, that serve as active pharmaceutical ingredients of vaccine compositions that stimulate anti-tumor immune responses. In particular, the present invention relates to two novel peptide sequences derived from HLA class I or II molecules of human oncofoetal antigen immature laminin receptor (OFA/iLR), which can be used in vaccine compositions for eliciting anti-tumor immune responses.
- 1. A tumor associated peptide comprising at least one peptide set forth in SEQ ID NO: 1 or SEQ ID NO: 2 provided that the peptide is not the intact human tumor associated polypeptide and wherein the peptide has the ability to bind to the human major histocompatibility complex (MHC) class-I HLA-A*0201 molecule.
- 5. (canceled)
- 8. (canceled)
- 11. (canceled)
- 16. (canceled)
- 18. (canceled)
- 22.-23. (canceled)
- 28. (canceled)
- 33. A tumor associated peptide that has the ability to bind to the human major histocompatibility complex (MHC) class-I HLA-A*0201 molecule and also bind to a human major histocompatibility complex (MHC) class-II molecule HLA-DRB1 molecule selected from the group consisting of *0101, *0301, *0401, *0701, *1501, wherein the peptide comprises the following motif:
B1-B2-B3-X1-B4-B5-X2-B6-X3-B7-B8-X4-B9-B10-B11
and wherein if the HLA-DRB1 is *0101, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is E, K, V, L, or W;
X2 is L, E or A;
X3 is A, P, or L; and
X4 is A, I, V, or R;
and wherein if the HLA-DRB1 is *0301, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is L, I, or K;
X2 is A, I or W;
X3 is R, N, or K; and
X4 is V, D or R;
and wherein if the HLA-DRB1 is *0401, then
B1, B2, B3, B4, B5, B6, B8, B9, B10 and B11 is any amino acid;
B7 is A, I, or P
X1 is L, I, or V;
X2 is A, I or E;
X3 is R, A, N or P; and
X4 is V, D or A;
and wherein if the HLA-DRB1 is *0701, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is L or I;
X2 is A or I;
X3 is R, N or A; and
X4 is V, D or A;
and wherein if the HLA-DRB1 is *1501, then
B1, B2, B3, B4, B5, B6, B8, B9, B10, B11 and X4 is any amino acid;
B7 is I, L, V or A
X1 is L, K or V;
X2 is A, W, R, or E; and
X3 is R, A, N or P.
- 34. A tumor associated peptide that has the ability to bind to the human major histocompatibility complex (MHC) class-I HLA-A*0201 molecule and also bind to a human major histocompatibility complex (MHC) class-II molecule HLA-DRB1 molecule selected from the group consisting of *0101, *0301, *0401, *0701, *1501, wherein the peptide comprises the following motif:
B1-B2-B3-X1-B4-B5-X2-B6-X3-B7-B8-X4-B9-B10-B11
and wherein if the HLA-DRB1 is *0101, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is Y or I;
X2 is L or C;
X3 is T; and
X4 is L or P;
and wherein if the HLA-DRB1 is *0301, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is C;
X2 is D;
X3 is P; and
X4 is Y;
and wherein if the HLA-DRB1 is *0401, then
B1, B2, B3, B4, B6, B6, B8, B9, B10 and B11 is any amino acid;
B7 is I, C or T
X1 is Y, L or T;
X2 is L or I;
X3 is T, L or N; and
X4 is L, T or S,
and wherein if the HLA-DRB1 is *0701, then
B1, B2, B3, B4, B5, B6, B7, B8, B9, B10 and B11 is any amino acid;
X1 is Y or L;
X2 is L or T;
X3 is T or S; and
X4 is L or R;
and wherein if the HLA-DRB1 is *1501, then
B1, B2, B3, B4, B5, B6, B8, B9, B10, B11 and X4 is any amino acid;
B7 is I, D or P
X1 is P, I or L;
X2 is Y, C or T; and
X3 is R, A, N or P.
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