IP Library › Granted Patent US 7,514,084
Granted Patent B2
US 7,514,084 · App. 10/527,496 · Granted Apr 7, 2009

KDR peptides and vaccines comprising the same

Assignee: Oncotherapy Science, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,514,084
App. No.
10/527,496
Granted
Apr 7, 2009
Kind
B2
Abstract

The present invention provides nonapeptides selected from peptides comprising the amino acid sequence of SEQ ID NO: 2, 3, 5, 8, 11, or 12; nonapeptides or decapeptides selected from peptides comprising the amino acid sequence of SEQ ID NO: 29, 30, 33, 34, 40, or 46; and peptides with cytotoxic T cell inducibility, in which one, two, or several amino acids are substituted or added to the above-mentioned amino acid sequences, as well as pharmaceuticals for treating or preventing tumors, where the pharmaceuticals comprise these peptides. The peptides of this invention can be used as vaccines.

Claims (10)

1. An isolated nonapeptide consisting of an amino acid sequence selected from the group consisting of SEQ ID NO: 30, and SEQ ID NO: 54, wherein zero, one or two amino acids have been substituted, wherein the nonapeptide binds to an HLA-A 0201 restricted T cell receptor with high affinity and induces a high CTL response.

2. The peptide of claim 1 , wherein the second amino acid from the N terminus is leucine or isoleucine.

3. The peptide of claim 1 , wherein the C-terminal amino acid is leucine.

4. A composition comprising one or more peptides of claim 1 .

5. The peptide of claim 1 , wherein said peptide consists of the amino acid sequence as set forth in SEQ ID NO:54.

6. The peptide of claim 1 , wherein said peptide consists of the amino acid sequence as set forth in SEQ ID NO: 30.

7. The peptide of claim 1 , wherein one or zero amino acids have been substituted.

8. The peptide of claim 7 , wherein the second amino acid from the N terminus is substituted.

9. The composition of claim 4 , further comprising a pharmaceutically acceptable carrier.

10. The composition of claim 4 , further comprising an adjuvant.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2006
From: TAHARA, HIDEAKI; WADA, SATOSHI; TSUNODA, TAKUYA
To: KIRIN BEER KABUSHIKI KAISHA
Reel/Frame 017167/0900 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2006
From: KIRIN BEER KABUSHIKI KAISHA
To: TAHARA, HIDEAKI
Reel/Frame 017167/0903 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2006
From: TAHARA, HIDEAKI
To: ONCOTHERAPY SCIENCE, INC.
Reel/Frame 017167/0924 →
Priority Claims (3)
JP 2002-267285 · Sep 12, 2002 · national
JP 2003-062003 · Mar 7, 2003 · national
JP 2003-167042 · Jun 11, 2003 · national
Continuity (1)
Related Publication 20060216301A1 · Sep 28, 2006