IP Library › Granted Patent US 11,364,309
Granted Patent B2
US 11,364,309 · App. 16/181,723 · Granted Jun 21, 2022

Neuronal enhancers

Inventors: Justin Cotney (Guilford, CT); Clifford Kentros (Malvik, NO); Stefan Blankvoort (Trondheim, NO); Rajeevkumar Raveendran Nair (Trondheim, NO)
Assignees: NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY (NTNU); UNIVERSITY OF CONNECTICUT
A61K48/0041A61K48/0058A61P25/28C12N5/10C12N7/00C12N15/113C12N2310/122C12N2310/3519C12N2310/531C12N2750/14143C12N2750/14171
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Quick Facts
Patent No.
US 11,364,309
App. No.
16/181,723
Granted
Jun 21, 2022
Kind
B2
Abstract

A delivery vehicle which comprises a nucleic acid construct, wherein the nucleic acid construct comprises (i) an enhancer which specifically drives gene expression in cells of the entorhinal cortex (ii) a promoter; and (iii) a therapeutic gene, wherein said enhancer, promoter and therapeutic gene are operatively linked, said enhancer and therapeutic gene are heterologous, and said delivery vehicle is suitable for delivery of the nucleic acid construct to the brain of a mammal.

Claims (18)

1. A delivery vehicle comprising a nucleic acid construct, wherein the nucleic acid construct comprises:

(i) an enhancer which specifically drives gene expression in cells of the entorhinal cortex, wherein the enhancer comprises a nucleotide sequence selected from SEQ ID NOs: 1-6, 9, and 10;

(ii) a promoter; and

(iii) a therapeutic gene,

wherein said enhancer, promoter and therapeutic gene are operatively linked, said enhancer and therapeutic gene are heterologous, and said delivery vehicle is suitable for delivery of the nucleic acid construct to the brain of a mammal.

2. The delivery vehicle of claim 1 , wherein said promoter is a minimal promoter.

3. The delivery vehicle of claim 1 , wherein said promoter is heterologous to said enhancer.

4. The delivery vehicle of claim 1 , wherein said enhancer specifically drives gene expression in cells of Layer II of the entorhinal cortex.

5. The delivery vehicle of claim 4 , wherein said enhancer specifically drives gene expression in reelin-positive cells.

6. The delivery vehicle of claim 1 , wherein said enhancer is human.

7. The delivery vehicle of claim 1 , wherein said promoter is selected from an HSP68 minimal promoter, a TRE3G promoter, a TRE3G minimal promoter, a TK minimal promoter, an FGF4 minimal promoter, an Odz3 minimal promoter, or a variant of any one or more of the foregoing promoters.

8. The delivery vehicle of claim 1 , wherein said delivery vehicle is a lipoplex, dendrimer, exosome or viral vector.

9. The delivery vehicle of claim 8 , wherein said viral vector is an adeno-associated virus (AAV).

10. The delivery vehicle of claim 1 , wherein said therapeutic gene encodes a protein or a functional RNA.

11. The delivery vehicle of claim 10 , wherein said functional RNA is an shRNA.

12. The delivery vehicle of claim 1 , wherein said therapeutic gene encodes an α secretase, neprilysin, PGC-1α, LSD1, an inhibitor of glycogen synthase kinase 3, or a Tau phosphorylation pseudosubstrate.

13. A cell comprising a nucleic acid construct as defined in claim 1 .

14. A composition comprising a delivery vehicle as defined in claim 1 and at least one physiologically-acceptable diluent, carrier or excipient.

Continuity (2)
Provisional Application 62584282 · Nov 10, 2017
Related Publication 20190247516A1 · Aug 15, 2019