IP Library Granted Patent US 10,214,741
Granted Patent B2
US 10,214,741 · App. 15/118,667 · Granted Feb 26, 2019

Methods and compositions for inhibiting retinopathy of prematurity

Inventor: Mary Elizabeth Hartnett (Salt Lake City, UT)
Assignee: UNIVERSITY OF UTAH RESEARCH FOUNDATION
C12N15/113C12N7/00C12N15/1136C12N15/1138C12N2310/141C12N2310/3519C12N2320/32C12N2330/51C12N2740/15031C12N2740/15043C12N2740/15045
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Quick Facts
Patent No.
US 10,214,741
App. No.
15/118,667
Granted
Feb 26, 2019
Kind
B2
Abstract

Disclosed are vectors and compositions comprising a pol II promoter and an shRNA wherein the shRNA has a sense RNA strand and an antisense RNA strand, wherein the sense and the antisense RNA strands form an RNA duplex, and wherein the sense RNA strand comprises a nucleotide sequence identical to a target sequence in STAT3, VEGFR, or EPOR. Also disclosed are methods of treating retinopathy of prematurity (ROP), methods of inhibiting expression of STAT3, VEGFR, and EPOR, and methods of regulating signaling events associated with intravitreal neovascularization (IVNV).

Claims (10)

1. A method of treating retinopathy of prematurity (ROP) comprising administering to a subject a composition comprising a vector, wherein the vector comprises a polymerase II (pol II) promoter and a first shRNA, wherein the first shRNA is embedded in microRNA, and wherein the first shRNA has a sense RNA strand and an antisense RNA strand, wherein the sense and the antisense RNA strands form an RNA duplex, wherein the sense RNA strand comprises a nucleotide sequence identical to a target sequence in STAT3, VEGFR2, or EPOR mRNA, and wherein the composition is administered via subretinal injection, wherein the first shRNA consists of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:25, SEQ ID NO:26, or SEQ ID NO:27.

2. The method of claim 1 , wherein the vector is a viral vector.

3. The method of claim 1 further comprising administering a second shRNA.

4. The method of claim 3 , wherein the second shRNA has a sense RNA strand and an antisense RNA strand, wherein the sense and the antisense RNA strands form an RNA duplex, and wherein the sense RNA strand comprises a nucleotide sequence identical to a target sequence in STAT3, VEGFR, or EPOR mRNA, and wherein the second shRNA is different than the first shRNA.

5. The method of claim 3 , wherein the second shRNA is in the same vector as the first shRNA.

6. The method of claim 3 , wherein the second shRNA is in a different vector than the first shRNA.

7. The method of claim 3 , wherein the second shRNA is administered in a separate composition from the first shRNA.

8. The method of claim 1 , wherein the pol II promoter is an endothelial cell-specific promoter.

9. The method of claim 8 , wherein the endothelial cell-specific promoter is a VE-cad promoter.

10. The method of claim 1 , wherein the intravitreal neovascularization (IVNV) phase of ROP in inhibited without interfering with physiologic retinal vascular development (PRVD).

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2018
From: HARTNETT, MARY ELIZABETH
To: UNIVERSITY OF UTAH
Reel/Frame 044823/0152 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2018
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 044823/0190 →
CONFIRMATORY LICENSE Recorded Oct 27, 2016
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040498/0777 →
Continuity (3)
Provisional Application 62008148 · Jun 5, 2014
Provisional Application 61940130 · Feb 14, 2014
Related Publication 20170051280A1 · Feb 23, 2017