IP Library Patent Application 17794225
Patent Application
App. No. 17/794,225

GENE THERAPY FOR NEURODEGENERATIVE DISORDERS USING POLYNUCLEOTIDE SILENCING AND REPLACEMENT

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Patent No.
US None
App. No.
17/794,225
Abstract

The disclosure relates to nucleic acid expression cassettes and vectors for the treatment of neurodegenerative disorders. Methods of treating neurodegenerative disorders such as Alzheimer's disease, frontotemporal dementia, frontotemporal lobar degeneration, Pick's disease, Lewy body dementia, memory loss, cognitive impairment, and mild cognitive impairment are also provided.

Claims (37)

1 . An expression cassette comprising:

a. a first polynucleotide encoding one or more short hairpin RNAs or (shRNAs) or micro RNAs (miRNAs), each of which independently targets a coding region or a non-coding region of an endogenous messenger RNA (mRNA) derived from each of a human wild-type and a mutant presenilin 1 (PSEN1) or from each of a human wild-type and a mutant presenilin 2 (PSEN2), wherein each of the one or more shRNAs or miRNAs is operably linked to one or more first promoters; and

b. a second polynucleotide encoding a wild-type presenilin 1 (PSEN1) or presenilin 2 (PSEN2) amino acid sequence, wherein the second polynucleotide is not targeted by any of the shRNAs or miRNAs encoded by the first polynucleotide; and wherein the second polynucleotide is operably linked to a second promoter.

2 . The expression cassette of claim 1 , wherein:

a. the first polynucleotide encodes one or more shRNAs or miRNAs, each of which independently targets a coding region or a non-coding region of an endogenous mRNA derived from each of a human wild-type and a mutant presenilin 1 (PSEN1); and

b. the second polynucleotide encodes a wild-type presenilin 1 (PSEN1), wherein the second polynucleotide is not targeted by any of the shRNAs or miRNAs encoded by the first polynucleotide.

3 . The expression cassette of claim 2 , wherein the first polynucleotide encodes one or more shRNAs or miRNAs, each of which independently comprises one of: a) SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:33, SEQ ID NO: 35, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO: 46, SEQ ID NO:47, nucleotides 448-529 of SEQ ID NO:76, nucleotides 448-529 of SEQ ID NO:77, or nucleotides 448-529 of SEQ ID NO:78; b) a modified version of any of the foregoing SEQ ID NOs, wherein the modification is 1, 2, 3, or 4 nucleotide changes; or c) a 19-21 base nucleotide sequence comprising 7 or more consecutive bases taken from the 5′ or 3′ end of any of the foregoing SEQ ID NOs or the modified version thereof, wherein the 19-21 base nucleotide sequence comprises no more than 4 mismatches with a corresponding portion of an endogenous PSEN1 mRNA.

4 . The expression cassette of claim 3 , wherein the first polynucleotide encodes one or more shRNAs or miRNAs, each of which independently comprises one of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:33, SEQ ID NO: 35, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO: 46, SEQ ID NO:47, nucleotides 448-529 of SEQ ID NO:76, nucleotides 448-529 of SEQ ID NO:77, or nucleotides 448-529 of SEQ ID NO:78.

5 . The expression cassette of claim 4 , wherein the first polynucleotide encodes one or more shRNAs or miRNAs, each of which independently comprises one of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:33, SEQ ID NO: 35, nucleotides 448-529 of SEQ ID NO:76, nucleotides 448-529 of SEQ ID NO:77, or nucleotides 448-529 of SEQ ID NO:78.

6 . The expression cassette of claim 5 , wherein the second polynucleotide comprises SEQ ID NO:39, or a polynucleotide that is codon optimized or modified as compared to SEQ ID NO:39.

7 . The expression cassette of claim 6 , wherein the second polynucleotide sequence comprises SEQ ID NO:39, SEQ ID NO:48, or nucleotides 1906-3303 of SEQ ID NO:68.

8 . The expression cassette of claim 4 , wherein at least one shRNA or miRNA comprises one of SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO: 42, or SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO: 46, SEQ ID NO:47, nucleotides 497-517 of SEQ ID NO:68, nucleotides 497-517 of SEQ ID NO:69, nucleotides 497-517 of SEQ ID NO:70, nucleotides 497-517 of SEQ ID NO:71.

9 . The expression cassette of claim 8 , wherein the second polynucleotide comprises a polynucleotide that is codon modified as compared to SEQ ID NO:39.

10 . The expression cassette of claim 9 , wherein the second polynucleotide sequence comprises SEQ ID NO:41, or nucleotides 1906-3303 of SEQ ID NO:68.

11 . The expression cassette of claim 1 , wherein at least one of the one or more first promoters is an RNA polymerase II or III promoter.

12 . The expression cassette of claim 11 , wherein each of the one or more first promoters is an RNA polymerase II or III promoter.

13 . The expression cassette of claim 11 , wherein the RNA polymerase III promoter is a U6 promoter, a U61 promoter, a U69 promoter, a H1 promoter, or any combination thereof; and the RNA polymerase II promoter is a ubiquitous or neuron-specific promoter.

14 . The expression cassette of claim 1 , wherein the second promoter is a RNA polymerase II promoter.

15 . The expression cassette of claim 14 , wherein the RNA polymerase II promoter is a ubiquitous or neuron-specific promoter.

16 . A vector comprising the expression cassette of claim 1 .

17 . A set of vectors comprising:

a. a first vector comprising an expression cassette comprising a first polynucleotide encoding one or more shRNAs or miRNAs targeting either a coding region or a non-coding region of a mRNA translated from each of a human wild-type and a mutant presenilin 1 (PSEN1), or from each of a human wild-type and a mutant presenilin 2 (PSEN2), wherein each of the one or more shRNAs or miRNAs is operably linked to one or more first promoters; and

b. a second vector comprising a second polynucleotide encoding a wild-type presenilin 1 (PSEN1) amino acid sequence or a wild-type presenilin 2 (PSEN2) amino acid sequence, wherein the second polynucleotide is not targeted by any of the shRNAs or miRNAs encoded by the first vector; and wherein the second polynucleotide is operably linked to a second promoter.

18 . The vector of claim 16 , wherein the vector or vectors are viral vectors.

19 . The vector of claim 18 , wherein the viral vectors are an adeno-associated virus (AAV) vector, a retroviral vector, a lentiviral vector, or an adenoviral vector.

20 . The vector of claim 19 , wherein the AAV vectors are AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAVDJ, AAVrh10, AAV11, AAV12, AAV2/1, AAV2/5, AAV2/6, AAV2/7, AAV2/8, AAV2/9, AAV2/rh10, AAV2/11, AAV2/12, PHP.B, and PHP.B derivatives [PHP.eR, PHP.S], AAV8[K137R], AAV-TT, rAAV-retro, AAV9.HR, AAV1 CAM mutants, or AAV9[586-590] swap mutants.

21 . A kit comprising the vector of claim 16 .

22 . A kit comprising:

a. one or more antisense oligonucleotides, wherein each antisense oligonucleotide independently targets either a coding region or a non-coding region of an mRNA translated from each of a human wild-type and mutant presenilin 1 (PSEN1), each of a human wild-type or mutant presenilin 2 (PSEN2); and

b. a vector comprising a polynucleotide encoding a wild-type presenilin 1 (PSEN1) amino acid sequence or a wild-type presenilin 2 (PSEN2) amino acid sequence, wherein the second polynucleotide is not targeted by any of the one or more antisense oligonucleotides; and wherein the polynucleotide is operably linked to a promoter in the vector.

23 . The kit of claim 22 , wherein each of the one or more antisense oligonucleotides is independently selected from a short hairpin RNA (shRNA), a short interfering RNA (siRNA), a micro interfering RNA (miRNA), a small temporal RNA (stRNA) or an endoribonuclease-prepared siRNA (esiRNA).

24 . The kit of claim 23 , wherein at least one of the one or more antisense oligonucleotides comprises one or more modified nucleobases.

25 . The kit of claim 24 , wherein each of the one or more modified nucleobases is independently selected from a non-naturally occurring nucleobase, a locked nucleic acids (LNA), or a peptide nucleic acids (PNA).

26 . A method of treating a neurodegenerative disease, disorder, or condition comprising administering to a subject in need thereof the vector of claim 16 .

27 . The method of claim 26 , wherein the neurodegenerative disease, disorder, or condition is Alzheimer's disease, sporadic Alzheimer's disease, familial Alzheimer's disease, frontotemporal dementia, frontotemporal lobar degeneration, Pick's disease, Lewy body dementia, memory loss, cognitive impairment, or mild cognitive impairment.

28 . An isolated nucleic acid sequence comprising SEQ ID NO: 41.

29 . A method of treating a neurodegenerative disease, disorder, or condition comprising administering to a subject in need thereof the set of vectors of claim 17 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2024
From: PAROS BIO, INC.
To: THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
Reel/Frame 068092/0937 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2024
From: GANNON, KIMBERLEY S.; GOULET, MARTIN; HACKETT, NEIL R.
To: PAROS BIO, INC.
Reel/Frame 068175/0981 →