IP Library Granted Patent US 7,452,864
Granted Patent B2
US 7,452,864 · App. 10/543,659 · Granted Nov 18, 2008

Use of the cathelicidin LL-37 and derivatives thereof for wound healing

Assignee: Lipopeptide AB
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Quick Facts
Patent No.
US 7,452,864
App. No.
10/543,659
Granted
Nov 18, 2008
Kind
B2
Abstract

Use of the antimicrobial cathelicidin peptide ll-37, N-terminal fragments of LL-37 or extended sequences of LL-37 having 1-3 amino acids in the C-terminal end, for stimulating proliferation of epithalial and stromal cells and thereby healing of wounds, such as chronic ulcers. The cytotoxic effect of LL-37 may be reduced by including a bilayer-forming polar lipid, especially a digalactosyldiacylglycerol, in pharmaceutical compositions and growth media comprising LL-37.

Claims (26)

1. A method of regenerating epithelial cells, healing of wound epithelium or healing of wound stroma, which comprises administering to a subject a peptide comprising an amino acid sequence containing at least 25 amino acids of the N-terminal fragment of SEQ ID NO: 1 or a pharmaceutically acceptable salt or ester or amide thereof, wherein said peptide enhances proliferation of epithelial and/or stromal cells through a non-lytic mechanism.

2. The method according to claim 1 , wherein the peptide is LL-37, SEQ ID NO: 1.

3. The method according to claim 1 , wherein the peptide is selected from the group consisting of LL-36, LL-35, LL-34, LL-33, LL-32, LL-31, LL-30, LL-29, LL-28, LL-27, LL-26, and LL-25, having the sequence SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, respectively.

4. The method according to claim 1 , wherein the peptide is in the form of an acetate salt.

5. The method according to claim 1 , wherein the peptide is LL-37 (SEQ ID NO:1) in the form of an acetate salt.

6. A pharmaceutical composition for topical application to epithelial cells comprising:

a) a peptide comprising an amino acid sequence containing at least 25 amino acids of the N-terminal fragment of LL-37 (SEQ ID NO: 1) or a pharmaceutically acceptable salt or ester or amide thereof; and

b) a bilayer forming polar lipid carrier comprising a galactolipid.

7. The pharmaceutical composition according to claim 6 , wherein the peptide is LL-37 (SEQ ID NO:1).

8. The pharmaceutical composition according to claim 6 , wherein the peptide is in the form of an acetate salt.

9. The pharmaceutical composition according to claim 6 , wherein the the peptide is selected from the group consisting of: LL-36, LL-35, LL-34, LL-33, LL-32, LL-31, LL-30, LL-29, LL-28, LL-27, LL-26, and LL-25, having the amino acid sequence SEQ ID NO: 2, SEQ LD NO: 3, SEQ ID NO: 4, SEQ II) NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13, respectively.

10. The pharmaceutical composition according to claim 6 , wherein the peptide is LL-37 in the form of an acetate salt.

11. The pharmaceutical composition according to claim 6 , further comprising an aqueous solution.

12. The pharmaceutical composition according to claim 6 , wherein the bilayer-forming polar lipid cater contains at least 50% (w/v) of a digalactosyldiacylglycerol.

13. The pharmaceutical composition according to claim 6 , wherein the bilayer-forming polar lipid cater contains 50 to 70% (w/w) of digalactosyldiacylglycerols and 30 to 50% (w/w) of other polar lipid.

14. The pharmaceutical composition according to claim 6 , wherein the ratio between the peptide as a salt and the bilayer-forming polar lipid cater is 1:10 to 1:50 by weight.

15. A bandage for wound healing comprising a pharmaceutical composition according to claim 6 .

16. A kit for culturing of epithelial and/or stromal cells comprising:

(a) a peptide comprising an amino acid sequence containing at least 25 amino acids of the N-terminal fragment of LL-37 (SEQ ID NO:1) or a pharmaceutically acceptable salt or ester or amide thereof; and

(b) a cytotoxicity reducing agent comprising a galactolipid.

17. The method according to claim 1 , wherein the subject has a chronic ulcer due to venous insufficiency, metabolic dysfunction, or immunological dysregulation.

18. The method according to claim 1 , wherein the subject has a wound due to trauma or a burn.

19. A growth medium for culturing epithelial and/or stromal cells comprising:

(a) a peptide comprising an amino acid sequence containing at least 25 amino acids of the N-terminal fragment of LL-37 (SEQ ID NO:1), or a pharmaceutically acceptable salt or ester or amide thereof;

(b) a cytotoxicity reducing agent comprising a galactolipid; and

(c) a basal medium.

Assignments (3)
CHANGE OF NAME Recorded Feb 15, 2017
From: LIPOPEPTIDE AB
To: PROMORE PHARMA AB
Reel/Frame 041794/0621 →
CHANGE OF ADDRESS Recorded Mar 28, 2014
From: STALE-BACKDAHL, MONA; HEILBORN, JOHAN; CARLSSON, ANDERS; BOGENTOFT, CONNY
To: LIPOPEPTIDE AB
Reel/Frame 032554/0897 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2005
From: STALE-BACKDAHL, MONA; HEILBORN, JOHAN; CARLSSON, ANDERS; BOGENTOFT, CONNY
To: LIPOPEPTIDE AB
Reel/Frame 017543/0185 →
Priority Claims (1)
SE 0300207 · Jan 29, 2003 · national
Continuity (2)
Provisional Application 6044496400 · Feb 5, 2003
Related Publication 20070149448A1 · Jun 28, 2007