IP Library Granted Patent US 10,485,849
Granted Patent B2
US 10,485,849 · App. 15/882,065 · Granted Nov 26, 2019

Syndecan peptides and polypeptides as inhibitors of vascular endothelial growth factor receptor-2 (VEGFR2) and very late antigen-4 (VLA-4)

Inventors: Alan Rapraeger (Stoughton, WI); Oisun Jung (Madison, WI)
Assignee: Wisconsin Alumni Research Foundation
A61K38/177A61K45/06
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Quick Facts
Patent No.
US 10,485,849
App. No.
15/882,065
Granted
Nov 26, 2019
Kind
B2
Abstract

Peptides from syndecan 1 and methods of use therefor are described. These peptides can inhibit very late antigen-4 (VLA-4) interaction with vascular endothelial growth factor-2 (VEGFR2), thereby preventing tumor cell growth and tissue invasion.

Claims (12)

1. A method of treating an inflammatory or autoimmune disease in a subject by inhibiting very late antigen-4 (VLA-4) interaction with syndecan-1, comprising contacting VLA-4 and/or syndecan-1 on the surface a cell within the subject that is associated with the inflammatory or autoimmune disease with a peptide segment consisting of between 12 and 100 amino acid residues and comprising amino acid residues 210-221, 210-233, 210-236, or 210-240 of SEQ ID NO:1;

whereby the inflammatory or autoimmune disease is treated.

2. The method of claim 1 , wherein the peptide segment is 12, 13, 14, 15, 16, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 40, 45, 49, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100 amino acid residues in length.

3. The method of claim 1 , wherein the peptide segment is between 12 and 50 amino acid residues in length.

4. The method of claim 1 , wherein the peptide segment is between 16 and 30 amino acid residues in length.

5. The method of claim 1 , wherein the peptide segment is between 23 and 27 amino acid residues in length.

6. The method of claim 1 , wherein the peptide segment consists essentially of amino acid residues 210-221 (SEQ ID NO:8), 210-233 (SEQ ID NO:4), 210-236 (SEQ ID NO:2), or 210-240 (SEQ ID NO:3) of SEQ ID NO:1.

7. The method of claim 1 , wherein the peptide segment comprises amino acid residues 210-221 (SEQ ID NO:8), 210-233 (SEQ ID NO:4), 210-236 (SEQ ID NO:2), or 210-240 (SEQ ID NO:3) of SEQ ID NO:1.

8. The method of claim 1 , wherein the peptide segment consists of amino acid residues 210-221 (SEQ ID NO:8), 210-233 (SEQ ID NO:4), 210-236 (SEQ ID NO:2), or 210-240 (SEQ ID NO:3) of SEQ ID NO:1.

9. The method of claim 1 , wherein the cell is an endothelial cell or a lymphoid cell.

10. The method of claim 1 , wherein contacting comprises providing an expression construct comprising a nucleic acid encoding the peptide segment.

11. The method of claim 1 , wherein the inflammatory or autoimmune disease that is treated is ulcerative colitis, Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus (SLE), or multiple sclerosis (MS).

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2018
From: RAPRAEGER, ALAN; JUNG, OISUN
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 045237/0614 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2018
From: RAPRAEGER, ALAN; JUNG, OISUN
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 044854/0608 →
CONFIRMATORY LICENSE Recorded Feb 5, 2018
From: UNIVERSITY OF WISCONSIN-MADISON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045248/0488 →
Continuity (3)
Division 15043951 · Feb 15, 2016
Provisional Application 62119466 · Feb 23, 2015
Related Publication 20180169185A1 · Jun 21, 2018