IP Library Granted Patent US 11,617,783
Granted Patent B2
US 11,617,783 · App. 15/776,714 · Granted Apr 4, 2023

Repairing a mutant human titin gene using CRISPR technology

Inventors: Louise Rodino-Klapac (E. Groveport, OH); Rachael Potter (Dublin, OH)
Assignee: RESEARCH INSTITUTE AT NATIONWIDE CHILDREN'S HOSPITAL
A61K38/39A61K48/00A61K48/005A61P21/00C07K14/4716C12N9/22C12N15/11C12N15/113C12N15/88C12N15/907C12N2310/20C12N2750/14143C12N2800/80
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Quick Facts
Patent No.
US 11,617,783
App. No.
15/776,714
Granted
Apr 4, 2023
Kind
B2
Abstract

The present application provides materials and methods for treating a patient with a titin-based myopathy, particularly a titin-based cardiomyopathy, and/or other titinopathy. In addition, the present application provides materials and methods for editing the titin gene in a cell by genome editing.

Claims (17)

1. A method of repairing a mutant titin gene in an isolated human cell comprising introducing into the cell

(a) a Cas9 endonuclease or a nucleic acid that encodes a Cas9 endonuclease; and

(b) (i) a nucleic acid encoding a guide ribonucleic acid (gRNA) comprising a spacer sequence having the nucleotide sequence set forth in SEQ ID NO: 19, 23, or 27-41 when the cell has a compound heterozygous mutation in exon 219 of the titin gene;

(ii) a nucleic acid encoding a gRNA comprising a spacer sequence having the nucleotide sequence set forth in SEQ ID NO: 64, 66, 68, 70, 72, 74, or 76 when the cell has a compound heterozygous mutation in exon 326 of the titin gene;

(iii) a nucleic acid encoding a gRNA comprising a spacer sequence having the nucleotide sequence set forth in SEQ ID NO: 1, 5, 9, or 13 and a nucleic acid comprising a donor template comprising the nucleotide sequence set forth in SEQ ID NO: 18 when the cell has a compound heterozygous c.32854G>C mutation in exon 219 of the titin gene; or

(iv) a nucleic acid encoding a gRNA comprising a spacer sequence having the nucleotide sequence set forth in SEQ ID NO: 57, 59, or 61 and a nucleic acid comprising a donor template comprising the nucleotide sequence set forth in SEQ ID NO: 63 when the cell has a compound heterozygous c.37112G>A mutation in intron 242 of the titin gene

resulting in repair of the mutant titin gene and expression of functional titin in the cell.

2. The method of claim 1 , wherein the isolated cell is an isolated heart cell.

3. The method of claim 1 , wherein the isolated cell is an isolated cardiac stem cell (CSC) or primary cardiomyocyte.

4. The method of claim 1 , wherein the nucleic acid is modified.

5. The method of claim 1 , wherein the gRNA is a single-molecule guide RNA (sgRNA).

6. The method of claim 5 , wherein the gRNA or the sgRNA is a modified gRNA or modified sgRNA.

7. The method of claim 1 , wherein the nucleic acid that encodes the Cas9 endonuclease and the nucleic acid that encodes the gRNA are introduced into the cell in a single vector.

8. The method of claim 1 , wherein the nucleic acid that encodes the Cas9 endonuclease and/or the nucleic acid comprising the donor template is/are introduced into the cell in a vector.

9. The method of claim 8 , wherein the vector is AAV.

10. The method of claim 1 , wherein the nucleic acid that encodes the Cas9 endonuclease, the nucleic acid that encodes the gRNA, and/or the nucleic acid comprising the donor template is/are introduced into the cell in a lipid nanoparticle.

11. The method of claim 1 , wherein the nucleic acid that encodes the Cas9 endonuclease introduced into the cell in a lipid nanoparticle and the nucleic acid that encodes the gRNA and/or donor DNA is introduced into the cell in a vector.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 5, 2018
From: RODINO-KLAPAC, LOUISE; POTTER, RACHAEL
To: RESEARCH INSTITUTE AT NATIONWIDE CHILDREN'S HOSPITAL
Reel/Frame 046786/0757 →
Continuity (2)
Provisional Application 62255887 · Nov 16, 2015
Related Publication 20180360921A1 · Dec 20, 2018