IP Library Granted Patent US 8,962,570
Granted Patent B2
US 8,962,570 · App. 13/473,758 · Granted Feb 24, 2015

Therapeutic use of peptide inhibitors of NADPH oxidase; aerosolization as a delivery mechanism

Inventor: Patrick J. Pagano (Sewickly, PA)
Assignee: University of Pittsburgh—of the Commonwealth System of Higher Education
A61K38/08A61K38/10
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Quick Facts
Patent No.
US 8,962,570
App. No.
13/473,758
Granted
Feb 24, 2015
Kind
B2
Abstract

A method is provided for treatment of a condition mediated by Nox2 in a patient. The method comprises administering to the patient by inhalation a polypeptide as described herein, able to inhibit superoxide production by Nox2. Conditions treatable in this manner include, without limitation, one or more of: right ventricular hypertrophy; pulmonary hypertension; acute lung injury; obstructive sleep apnea; ischemia/reperfusion injury in the lung; pulmonary fibrosis; an obstructive lung disorder such as Chronic Obstructive Pulmonary Disease (COPD), asthma, cystic fibrosis and emphysema; and atherosclerosis.

Claims (10)

1. A method of treating a condition of the heart, lungs, or blood vessels connecting the heart and the lungs mediated by Nox2 in a patient, comprising decreasing superoxide anion production by Nox2 in an amount and duration effective to relieve one or more symptoms of the condition in the patient by administering to the patient by inhalation an aerosolized polypeptide consisting of: a) a 9-12 amino acid fragment comprising the amino acid sequence CSTRIRRQL (SEQ ID NO: 6) and b) a tat cell penetration peptide, wherein the tat cell penetration peptide is conjugated to the amino acid fragment, and wherein the condition is one or more of right ventricular hypertrophy, pulmonary hypertension, acute lung injury, obstructive sleep apnea, ischemia/reperfusion injury in the lung, and pulmonary fibrosis.

2. The method of claim 1 , wherein aerosolized polypeptide consists of RKKRRQRRRCSTRIRRQL (SEQ ID NO: 7).

3. The method of claim 1 , wherein the condition is right ventricular hypertrophy.

4. The method of claim 1 , wherein the condition is pulmonary hypertension.

5. The method of claim 1 , wherein the condition is acute lung injury.

6. The method of claim 1 , wherein the condition is pulmonary fibrosis.

7. The method of claim 1 , wherein the condition is obstructive sleep apnea.

8. The method of claim 1 , wherein the condition is ischemia/reperfusion injury in the lung.

9. The method of claim 1 , wherein the tat cell penetration peptide consists of RKKRRQRRR (SEQ ID NO: 13).

10. The method of claim 1 , wherein the fragment a) consists of CSTRIRRQL (SEQ ID NO: 6).

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 18, 2012
From: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029003/0790 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 24, 2012
From: PAGANO, PATRICK J.
To: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 028844/0630 →
Continuity (2)
Provisional Application 61486837 · May 17, 2011
Related Publication 20120316100A1 · Dec 13, 2012