US2011142919A1PendingUtilityA1

Cytotoxic T-Lymphocyte-Inducing Immunogens for Prevention, Treatment and Diagnosis of Cancer

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Assignee: IMMUNOTOPE INCPriority: Dec 4, 2000Filed: Feb 18, 2011Published: Jun 16, 2011
Est. expiryDec 4, 2020(expired)· nominal 20-yr term from priority
A61K 38/19A61K 2039/53A61K 9/127C07K 14/47C07K 14/71A61K 2039/812C07K 14/485C07K 14/705A61K 38/18C07K 14/4748C07K 14/70546A61K 2039/522C07K 14/4738A61P 35/00A61P 37/04G01N 33/5758A61K 40/42A61K 40/11A61K 39/0011C12N 5/0636A61K 39/00
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Claims

Abstract

The present invention relates to compositions and methods for the prevention, treatment, and diagnosis of cancer, especially carcinomas, such as ovarian carcinoma. The invention discloses peptides, polypeptides, and polynucleotides that can be used to stimulate a CTL response against cancer.

Claims

exact text as granted — not AI-modified
1 . A method for eliciting a CTL response against tumor cells presenting at least one of the following epitopic peptides: SEQ ID NO: 1516, 1517, 1519, 1521, 1527, 1528, or 1529 in a subject, comprising administering to said subject a composition comprising
 at least one polypeptide comprising an epitopic peptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1516, 1517, 1519, 1521, 1527, 1528, and 1529 in an amount sufficient to induce a CTL response to said tumor cells; or   at least one polypeptide comprising an epitopic peptide having no more than one amino acid difference from an amino acid sequence selected from the group consisting of SEQ ID NO: 1516, 1517, 1519, 1521, 1527, 1528, and 1529 in an amount sufficient to induce a CTL response to said tumor cells.   
     
     
         2 . The method of  claim 1 , wherein said amino acid difference is the result of a conservative amino acid substitution. 
     
     
         3 . The method of  claim 1 , wherein said amino acid difference is the result of a substitution of one hydrophobic amino acid with another hydrophobic amino acid. 
     
     
         4 . The method of  claim 1 , wherein said amino acid difference is the result of an addition or deletion of one amino acid to or from said epitopic peptide. 
     
     
         5 . The method of  claim 1 , wherein said composition further comprises an adjuvant. 
     
     
         6 . The method of  claim 5 , wherein said adjuvant is selected from the group consisting of complete Freund's adjuvant, incomplete Freund's adjuvant, Montanide ISA-51, LAG-3, aluminum phosphate, aluminum hydroxide, alum, and saponin. 
     
     
         7 . The method of  claim 1 , wherein said composition further comprises a cytokine. 
     
     
         8 . The method of  claim 7 , wherein said cytokine is GM-CSF. 
     
     
         9 . The method of  claim 1 , wherein said composition further comprises a vehicle. 
     
     
         10 . The method of  claim 9 , where said vehicle is selected from the group consisting of a liposome, an immunostimulating complex (ISCOM), and slow-releasing particles. 
     
     
         11 . The method of  claim 10 , wherein said liposome comprises an emulsion, a foam, a micelle, an insoluble monolayer, a liquid crystal, a phospholipid dispersion, or a lamellar layer. 
     
     
         12 . The method of  claim 1 , wherein said polypeptide consists of
 an amino acid sequence selected from the group consisting of SEQ ID NO: 1516, 1517, 1519, 1521, 1527, 1528, and 1529; or   an amino acid sequence having no more than one amino acid differences from an amino acid sequence selected from the group consisting of SEQ ID NO: 1516, 1517, 1519, 1521, 1527, 1528, and 1529.   
     
     
         13 . The method of  claim 1 , wherein said tumor cells are part of a carcinoma. 
     
     
         14 . The method of  claim 1 , wherein said cancer is tumor cells are part of an ovarian carcinoma. 
     
     
         15 . The method of  claim 1 , wherein said polypeptide comprises at least two epitopic peptides. 
     
     
         16 . The method of  claim 15 , wherein said polypeptide comprises at least three epitopic peptides. 
     
     
         17 . The method of  claim 1 , wherein said composition comprises
 an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1516;   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1517;   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1519;   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1521;   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1527;   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1528; and   an epitopic peptide comprising an amino acid sequence of SEQ ID NO: 1529.

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