IP Library Granted Patent US 11,744,851
Granted Patent B2
US 11,744,851 · App. 17/467,555 · Granted Sep 5, 2023

Enhancing AAV-mediated transduction of ocular tissues with hyaluronic acid

Inventors: Shannon E. Boye (Gainesville, FL); Sanford L. Boye (Gainesville, FL)
Assignee: University of Florida Research Foundation, Incorporated
A61K31/728A61K9/0019A61K9/5184A61K35/761A61P17/00C07K16/2875A61K2039/5258A61K2800/91
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Quick Facts
Patent No.
US 11,744,851
App. No.
17/467,555
Granted
Sep 5, 2023
Kind
B2
Abstract

Disclosed herein are compositions of rAAV particles and methods for administrating rAAV particles having enhanced transduction properties.

Claims (18)

1. A composition comprising a rAAV particle comprising: (a) a capsid admixed with hyaluronic acid and (b) a polynucleotide encoding a therapeutic agent, wherein the hyaluronic acid has an average molecular weight of 4 kDa to 5,000 kDa, wherein the therapeutic agent (a) preserves one or more photoreceptor cells, one or more retinal ganglion cells, one or more retinal bipolar cells, or one or more retinal pigment epithelial (RPE) cells; (b) restores one or more rod-and/or cone-mediated functions; (c) restores visual behavior in one or both eyes; or (d) any combination thereof.

2. The composition of claim 1 , wherein the hyaluronic acid has an average molecular weight of 20 kDa to 5,000 kDa.

3. The composition of claim 1 , wherein the hyaluronic acid is present at a concentration of 0.1% to 1.0% weight by volume.

4. A composition comprising a rAAV particle comprising: (a) a capsid admixed with hyaluronic acid and (b) a polynucleotide encoding a therapeutic agent, wherein the hyaluronic acid has an average molecular weight of 4 kDa to 5,000 kDa, wherein the polynucleotide is operably linked to a regulatory sequence that directs expression of the polynucleotide in a retinal ganglion cell.

5. A composition comprising a rAAV particle comprising: (a) a capsid admixed with hyaluronic acid and (b) a polynucleotide encoding a therapeutic agent, wherein the hyaluronic acid has an average molecular weight of 4 kDa to 5,000 kDa, wherein the therapeutic agent is a neurotrophic factor or an optogenetic actuator.

6. The composition of claim 5 , comprising the neurotropic factor, wherein the neurotropic factor comprises brain derived neurotrophic factor (BDNF), nerve growth factor (NGF), neurotrophin-3, ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), an ephrin, or glial cell line-derived neurotrophic factor (GDNF); or a combination of two or more thereof.

7. The composition of claim 5 , comprising the optogenetic actuator, wherein the optogenetic actuator comprises a bacteriorhodopsin, a halorhodopsin, a channelrhodopsin, a microbial sensory rhodopsin, a mammalian rhodopsin, a cone opsin, or a melanopsin; or a combination of two or more thereof.

8. The composition of claim 1 , comprising a promoter operably linked to the polynucleotide encoding the therapeutic agent.

9. The composition of claim 8 , wherein the promoter is a photoreceptor specific promoter or a retinal pigment epithelial (RPE) cell-specific promoter.

10. The composition of claim 8 , wherein the promoter is a smCBA promoter, a rhodopsin kinase promoter, an IRBP promoter, a bipolar cell promoter, an NRL promoter, a GNAT2 promoter, an opsin promoter, a cone arrestin promoter, a VMD2 (BEST1) promoter, or a RPE65 promoter.

11. The composition of claim 1 , wherein the rAAV particle is present in the composition in a titer having a range of about 1×10 10 vector genomes (vg)/ml to about 5×10 13 vg/ml.

12. The composition of claim 1 , wherein the rAAV particle comprises a capsid selected from AAV2, AAV2(Y444F), AAV2(trpYF), AAV2 (quadYF), AAV2(quadYF+T−V), AAV2/2−MAX, DGE−DF, ME−B, ME−B(Y−F+T−V), P2−V2, and P2−V3.

13. The composition of claim 1 , wherein the rAAV particle comprises a capsid selected from AAV6, AAV7m8, AAV-DJ, AAV3, AAV3b, AAV6-3 pMut, AAVSHh10, AAVSHh10Y, and AAVLK03.

14. The composition of claim 1 , wherein the composition is formulated for intravitreal injection.

15. The composition of claim 14 , wherein the composition is formulated with one or more excipients from the group comprising balanced salt solution, polysorbate 20, poloxamer 188, and TMN200.

16. The composition of claim 14 , wherein the composition is formulated with balanced salt solution and polysorbate 20.

17. The composition of claim 14 , wherein the composition is formulated with poloxamer 188 and TMN200.

18. The composition of claim 4 , wherein the regulatory sequence is selected from the group consisting of: a woodchuck hepatitis virus post-transcription regulatory element (WPRE), a polyadenylation signal sequence, an intron/exon junction/splicing signal, or a combination thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Dec 13, 2023
From: UNIVERSITY OF FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 065968/0398 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: BOYE, SHANNON E.; BOYE, SANFORD L.
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 058458/0647 →
Continuity (3)
Continuation 16914230 · Jun 26, 2020
Provisional Application 62867596 · Jun 27, 2019
Related Publication 20220062325A1 · Mar 3, 2022
Cited By (1)
US 12,605,466