IP Library Granted Patent US 10,981,961
Granted Patent B2
US 10,981,961 · App. 14/775,289 · Granted Apr 20, 2021

Delivery of card protein as therapy for occular inflammation

Inventors: Cristhian J. Ildefonso (Gainesville, FL); Alfred S. Lewin (Gainesville, FL); Qiuhong Li (Gainesville, FL)
Assignee: University of Florida Research Foundation, Incorporated
C07K14/4703A61K9/0048A61K48/005A61K38/00A61K48/00C07K2319/02C07K2319/03C07K2319/10C12N15/86C12N2740/15041C12N2750/14141
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Quick Facts
Patent No.
US 10,981,961
App. No.
14/775,289
Granted
Apr 20, 2021
Kind
B2
Abstract

The present invention provides methods and compositions for treating and/or preventing age related macular degeneration and other conditions involving macular degeneration, ocular neovascularization, or ocular inflammation. In an exemplary embodiment, a method is disclosed that involves administering an expression vector that delivers a secretable and cell penetrating CARD to a subject in need of treatment or prevention of age-related macular degeneration or another condition involving macular degeneration or ocular neovascularization.

Claims (10)

1. A method for the amelioration or treatment of an ocular disease or ocular condition in a subject, the method comprising:

intravitreally administering a therapeutically effective amount of a viral vector comprising an expression construct comprising (a) a nucleotide sequence encoding a fusion protein comprising a cell-penetrating peptide derived from the HIV Tat protein (Tat) and a Caspase Activation and Recruitment Domain (CARD) and (b) a nucleotide sequence encoding a secretion signal peptide to the subject's eye, wherein the Tat comprises amino acids 1-9 of the amino acid sequence of SEQ ID NO: 1 and the CARD comprises amino acids 10-100 of the amino acid sequence of SEQ ID NO: 1

wherein the ocular disease or ocular condition is selected from the group consisting of ocular inflammation, macular degeneration, age-related macular degeneration (AMD), geographic atrophy, wet AMD, dry AMD, drusen formation, dry eye, diabetic retinopathy, vitreoretinopathy, corneal inflammation, uveitis, ocular hypertension and glaucoma.

2. The method of claim 1 , wherein said viral vector is an AAV vector.

3. The method of claim 1 , wherein said viral vector is a retroviral vector, a lentiviral vector, an adenoviral vector, a Herpes viral vector, a Hepatitis viral vector, an SV40 vector, an EBV vector, an adeno-associated virus (AAV) vector or a nonviral vector.

4. The method of claim 1 , wherein said method comprises treating a subject who exhibits one or more of the following symptoms: drusen formation, eye pain, eye redness, light sensitivity, tearing, or blurred vision.

5. The method of claim 4 , wherein said method comprises treating a subject who exhibits two or more of the following symptoms: drusen, eye pain, eye redness, light sensitivity, tearing, or blurred vision.

6. The method of claim 4 , wherein said subject exhibits drusen formation.

7. The method of claim 2 , wherein the AAV vector is an AAV2 vector.

8. The method of claim 1 , wherein the secretion signal peptide is an IgK signal peptide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2016
From: ILDEFONSO, CRISTHIAN J.; LEWIN, ALFRED S.; LI, QIUHONG
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 037666/0853 →
Continuity (1)
Related Publication 20160017012A1 · Jan 21, 2016
Cited By (1)
US 12,415,841