IP Library › Granted Patent US 9,018,169
Granted Patent B2
US 9,018,169 · App. 13/981,238 · Granted Apr 28, 2015

Peptides for suppressing inflammation

Inventors: Daniel T. Laskowitz (Chapel Hill, NC); Hana Dawson (Cary, NC); Brad Kolls (Durham, NC)
Assignee: Duke University
C07K7/06A61K38/00C07K14/775
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 9,018,169
App. No.
13/981,238
Granted
Apr 28, 2015
Kind
B2
Abstract

Provided herein are peptides that exhibit ApoE biological activity, as well as compositions and pharmaceutical formulations that include the peptides. The peptides, compositions, and methods disclosed herein have broad applications as they can be used to treat a broad spectrum of injury, diseases, disorders, and clinical indications.

Claims (21)

1. An isolated pentapeptide of Formula I:

(SEQ ID NO: 1)

X1-X2-X3-X4-X5

or a salt thereof, wherein

X1 is V;

X2 is S;

X3 is K or R;

X4 is K or R; and

X5 is R;

and wherein said pentapeptide is optionally N-terminal acetylated and/or C-terminal amidated.

2. The isolated pentapeptide of claim 1 , wherein said pentapeptide is N-terminal acetylated and/or C-terminal amidated.

3. The pentapeptide of claim 2 , wherein said pentapeptide is N-terminal acetylated and/or C-terminal amidated and has the amino acid sequence of VSRKR (SEQ ID NO:2), VSKRR (SEQ ID NO:3), or VSRRR (SEQ ID NO:4).

4. The pentapeptide of claim 1 , wherein said pentapeptide is VSKRR (SEQ ID NO:3) modified by both N-terminal acetylation and C-terminal amidation.

5. The pentapeptide of claim 1 , wherein said pentapeptide is VSRRR (SEQ ID NO: 4) modified by both N-terminal acetylation and C-terminal amidation.

6. A method of reducing inflammation in a subject in need thereof, the method comprising administering to the subject an effective amount of a pentapeptide of claim 1 .

7. The method of claim 6 , comprising administering the pentapeptide by an injection, inhalation, transdermal, intravenous, intranasal, intracranial, and/or intrathecal route.

8. A composition comprising the pentapeptide of claim 1 and a pharmaceutically acceptable carrier, vehicle, diluent, or adjuvant.

9. A composition comprising the pentapeptide of claim 2 and a pharmaceutically acceptable carrier, vehicle, diluent, or adjuvant.

10. A composition comprising the pentapeptide of claim 3 and a pharmaceutically acceptable carrier, vehicle, diluent, or adjuvant.

11. A composition comprising the pentapeptide of claim 4 and a pharmaceutically acceptable carrier, vehicle, diluent, or adjuvant.

12. A composition comprising the pentapeptide of claim 5 and a pharmaceutically acceptable carrier, vehicle, diluent, or adjuvant.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2013
From: LASKOWITZ, DANIEL T.; KOLLS, BRAD; DAWSON, HANA
To: DUKE UNIVERSITY
Reel/Frame 031529/0052 →
Continuity (2)
Provisional Application 61454342 · Mar 18, 2011
Related Publication 20140038898A1 · Feb 6, 2014