IP Library Granted Patent US 11,993,787
Granted Patent B2
US 11,993,787 · App. 15/770,881 · Granted May 28, 2024

Neural cell extracellular vesicles

Inventors: Steven L. Stice (Athens, GA); Robin Lynn Webb (Winterville, GA); Tracy A. Stice (Athens, GA)
Assignees: UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC.; Aruna Bio, Inc.
C12N5/0619A61K9/5176A61K35/12A61K35/545C12N5/0622C12N5/0623A61K9/5068A61K35/30A61P25/28C12N2506/02C12N2506/45C12N2533/30G01N33/56966
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Quick Facts
Patent No.
US 11,993,787
App. No.
15/770,881
Granted
May 28, 2024
Kind
B2
Abstract

Disclosed herein are neural extracellular vesicles (EVs) and methods of using these EVs in the treatment of spinal cord injury, stroke, and traumatic brain injury and neurodegenerative diseases.

Claims (14)

1. A pharmaceutical composition comprising a therapeutically effective amount of extracellular vesicles (EVs) obtained from non-transformed human neural progenitor cells that are capable of differentiating into neurons, astrocytes and oligodendrocytes in vitro, and a pharmaceutically acceptable carrier, wherein the EVs comprise melanoma-associated chondroitin sulfate proteoglycan (MCSP), pentraxin-3 (PTX3), angiopoietin-1, insulin-like growth factor-binding protein 2 (IGFBP2), macrophage colony-stimulating factor, and ecto-5′-nucleotidase (NT5E), and wherein the EVs comprise an exogenous agent selected from the group consisting of an siRNA, an antisense oligonucleotide, a peptide, a protein, an antibody, and a small molecule.

2. The pharmaceutical composition of claim 1 , wherein the EVs comprise an exogenous siRNA.

3. The pharmaceutical composition of claim 1 , wherein the EVs comprise an exogenous antisense oligonucleotide.

4. The pharmaceutical composition of claim 1 , wherein the EVs comprise an exogenous peptide or an exogenous protein.

5. The pharmaceutical composition of claim 1 , wherein the EVs comprise an antibody.

6. The pharmaceutical composition of claim 1 , wherein the EVs comprise a small molecule.

7. The pharmaceutical composition of claim 1 , wherein the EVs are exosomes.

8. The pharmaceutical composition of claim 1 , wherein the composition comprises about 1 mg to about 750 mg of EVs.

9. The pharmaceutical composition of claim 1 , wherein the EVs are about 20 nm to 10 μm in size.

10. The pharmaceutical composition of claim 1 , wherein the EVs are about 25 nm to about 250 nm in size.

11. The pharmaceutical composition of claim 1 , wherein the neural progenitor cells are obtained from human pluripotent stem cells.

12. The pharmaceutical composition of claim 1 , wherein the neural progenitor cells are obtained from human induced pluripotent stem cells.

13. The pharmaceutical composition of claim 1 , wherein the neural progenitor cells are obtained from human embryonic stem cells.

14. The pharmaceutical composition of claim 1 , wherein the neural progenitor cells are SOX1 + , SOX2 + and OCT4 − .

Assignments (4)
CHANGE OF NAME Recorded Oct 21, 2022
From: ARUNA BIOMEDICAL, INC.
To: ARUNA BIO, INC.
Reel/Frame 061744/0925 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2021
From: STICE, STEVEN L.; WEBB, ROBIN LYNN
To: UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC.
Reel/Frame 056273/0865 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2021
From: STICE, TRACEY A.
To: ARUNA BIOMEDICAL, INC.
Reel/Frame 056274/0861 →
CONFIRMATORY LICENSE Recorded Oct 3, 2018
From: UNIVERSITY OF GEORGIA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 047190/0051 →
Continuity (2)
Provisional Application 62256823 · Nov 18, 2015
Related Publication 20180327714A1 · Nov 15, 2018
Cited By (1)
US 12,624,343