IP Library Granted Patent US 8,536,117
Granted Patent B2
US 8,536,117 · App. 13/396,098 · Granted Sep 17, 2013

Oxidant resistant apolipoprotein A-1 and mimetic peptides

Inventors: Jonathan D. Smith (Shaker Heights, OH); Stanley L. Hazen (Pepper Pike, OH)
Assignee: The Cleveland Clinic Foundation
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Quick Facts
Patent No.
US 8,536,117
App. No.
13/396,098
Granted
Sep 17, 2013
Kind
B2
Abstract

A method for the treatment of cardiovascular disease or disorder in a subject in need thereof, the method comprising the steps of administering an ApoA1 mimetic that is capable of promoting cholesterol efflux from lipid loaded cells in the subject, wherein the ApoA1 mimetic has an amino acid sequence that includes at least a portion of the amino acid sequence of ApoA1 or a mimetic of ApoA1 that contains at least one tryptophan, at least one tryptophan from the ApoA1 or mimetic of the ApoA1 being substituted with an oxidant resistant amino acid in the amino acid sequence of the ApoA1 mimetic.

Claims (17)

1. A method of treating a cardiovascular disorder in a subject in need thereof, the method comprising the step of:

administering to the subject a therapeutically effective amount of a polypeptide that is capable of promoting cholesterol efflux from lipid loaded cells, the polypeptide consisting of the amino acid sequence of SEQ ID NO:1, in which each X in SEQ ID NO:1 is a phenylalanine amino acid.

2. The method according to claim 1 , wherein the polypeptide is a purified polypeptide.

3. The method according to claim 1 , wherein the polypeptide is a recombinant polypeptide.

4. The method according to claim 3 , wherein the recombinant polypeptide is produced in bacteria, yeast, plant, insect, avian, or mammalian cells.

5. The method according to claim 1 , wherein the cardiovascular disorder is: aneurysms, angina, arrhythmia, atherosclerosis, arteriosclerosis, cardiomyopathy, cerebrovascular disease, congenital heart disease, congestive heart failure, coronary artery disease, hyperlipidemia, hypercholesterolemia, myocarditis, valve disease, dilated cardiomyopathy, diastolic dysfunction, endocarditis, hypertension, hypertrophic cardiomyopathy, mitral valve prolapse, heart attack, vascular stenosis or venous thromboembolism.

6. A method of treating a cardiovascular disorder in a subject in need thereof, the method comprising the step of administering a therapeutically effective amount of a pharmaceutical composition that is capable of promoting cholesterol efflux from lipid loaded cells, the pharmaceutical composition comprising a polypeptide and a pharmaceutically acceptable excipient, wherein said polypeptide consists of the amino acid sequence of SEQ ID NO:1, in which each X in SEQ I D NO:1 is a phenylalanine amino acid.

7. The method according to claim 6 , wherein the polypeptide is a purified polypeptide.

8. The method according to claim 6 , wherein the composition is formulated for administration to the subject by a route selected from the group consisting of: oral administration, nasal administration, rectal administration, intraperitoneal injection, intravascular injection, subcutaneous injection, transcutaneous administration, inhalation administration, and intramuscular injection.

9. The method according to claim 8 , wherein said composition is formulated as a unit dosage formulation.

10. The method according to claim 9 , wherein the pharmaceutical composition is formulated for intravascular administration, subcutaneous injection, transcutaneous administration, or intramuscular injection.

11. The method according to claim 10 , wherein the pharmaceutical composition comprises polymeric, hydrophobic materials, or ion exchange resins.

12. The method according to claim 8 , wherein the pharmaceutical composition is formulated for intravascular administration.

13. The method according to claim 8 , wherein the pharmaceutical composition comprises a powdered form of the polypeptide and a vehicle.

14. The method according to claim 13 , wherein the vehicle comprises sterile pyrogen free water, buffer, or dextrose solution.

15. The method according to claim 13 , wherein the powdered form of the polypeptide comprises lyophilized powdered polypeptide.

16. The method according to claim 6 , wherein the cardiovascular disorder is: aneurysms, angina, arrhythmia, atherosclerosis, arteriosclerosis, cardiomyopathy, cerebrovascular disease, congenital heart disease, congestive heart failure, coronary artery disease, hyperlipidemia, hypercholesterolemia, myocarditis, valve disease, dilated cardiomyopathy, diastolic dysfunction, endocarditis, hypertension, hypertrophic cardiomyopathy, mitral valve prolapse, heart attack, vascular stenosis or venous thromboembolism.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2012
From: SMITH, JONATHAN D.; HAZEN, STANLEY L.
To: THE CLEVELAND CLINIC FOUNDATION
Reel/Frame 028065/0323 →
Continuity (3)
Division 12256822 · Oct 23, 2008
Provisional Application 60981887 · Oct 23, 2007
Related Publication 20120264677A1 · Oct 18, 2012