US2013230547A1PendingUtilityA1
Methods and compositions for prostate cancer immunotherapy
Est. expiryMay 1, 2028(~1.8 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 37/04A61K 45/06A61K 38/10A61P 13/08A61K 38/08A61K 40/4275A61K 40/11A61K 2239/58A61K 39/0011
33
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Claims
Abstract
The present invention features methods and compositions (e.g., immune response stimulating peptides (e.g., ERG or SIM2 peptides), activated immune cells, antigen-presenting cells, and antibodies or antigen-binding fragments thereof) for generating an immune response for the treatment of cancer (e.g., prostate cancer).
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for treating prostate cancer in a subject comprising administering to said subject a composition comprising a peptide having a sequence with at least 90% sequence identity to SEQ ID NO: 3, wherein said peptide has at least 7 but fewer than 50 amino acid residues.
2 . The method of claim 1 , wherein said peptide comprises the sequence of SEQ ID NO: 3.
3 . The method of claim 1 , wherein said peptide comprises a sequence having at least 90% sequence identity to amino acids 319 to 330 of SEQ ID NO:1.
4 . The method of claim 3 , wherein said peptide comprises amino acids 319 to 330 of SEQ ID NO: 1.
5 . The method of claim 1 , wherein said peptide comprises a sequence having at least 90% sequence identity to amino acids 308 to 333 of SEQ ID NO: 1.
6 . The method of claim 5 , wherein said peptide comprises amino acids 308 to 330 of SEQ ID NO: 1.
7 . The method of claim 1 , wherein said peptide comprises the sequence of any one of SEQ ID NOs: 33-38.
8 . The method of claim 1 , wherein said peptide is capable of activating immune cells in said subject when all or a portion of said peptide is bound to an antigen-presenting molecule.
9 . The method of claim 8 , wherein said immune cells are cytotoxic T lymphocytes.
10 . The method of claim 8 , wherein said antigen-presenting molecule is an HLA molecule.
11 . The method of claim 10 , wherein said HLA molecule is an HLA class I molecule.
12 . The method of claim 1 , wherein said subject is a human.
13 . The method of claim 1 , wherein said peptide is conjugated to a heterologous compound.
14 . The method of claim 13 , wherein said heterologous compound is a therapeutic or cytotoxic agent.
15 . The method of claim 1 , wherein said composition is a vaccine.
16 . The method of claim 15 , wherein said composition comprises an adjuvant or an additional therapeutic agent.
17 . The method of claim 1 , wherein said method further comprises administering a cytokine or hormone therapy.
18 . The method of claim 17 , wherein said hormone therapy comprises androgen ablation.
19 . The method of claim 1 , wherein said composition comprises a pharmaceutically acceptable diluent, excipient, or carrier.
20 . The method of claim 1 , wherein said composition is formulated for oral, topical, sublingual, nasal, intraoptical, vaginal, or rectal administration, for administration by inhalation, or for intramuscular, intraperitoneal, intravenous, or intradermal injection.
21 . The method of claim 1 , wherein said composition comprises an isolated antigen-presenting cell comprising a surface-bound antigen-presenting molecule, wherein said peptide is bound to said antigen-presenting molecule.
22 . The method of claim 21 , wherein said antigen-presenting cell is a dendritic cell or a macrophage, and wherein said antigen-presenting molecule is an HLA class I molecule.Join the waitlist — get patent alerts
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