US2023073246A1PendingUtilityA1

Bag3 as a target for therapy of heart failure

70
Assignee: UNIV TEMPLEPriority: Jan 31, 2014Filed: Oct 5, 2022Published: Mar 9, 2023
Est. expiryJan 31, 2034(~7.6 yrs left)· nominal 20-yr term from priority
A61P 9/06G01N 2800/325A61P 9/00G01N 2500/04C12Q 2600/158A61P 31/12A61K 48/00G01N 33/6893G01N 33/6887C12Q 2600/106G01N 2500/10C12Q 2600/156G01N 2800/50A61P 17/02C12Q 1/6883A61P 29/00A61P 9/10A61P 9/04A61P 9/12A61P 21/00A61P 35/00
70
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Claims

Abstract

Compositions are directed to BCL2-associated athanogene 3 (BAG3) molecules and agents which modulate expression of BAG3 molecules. Pharmaceutical composition for administration to patients, for example, patients with heart failure, comprise one or more BAG3 molecules or agents which modulate expression of BAG3. Methods of treatment and identifying candidate therapeutic agents are also provided.

Claims

exact text as granted — not AI-modified
1 .- 49 . (canceled) 
     
     
         50 . A method of treating a human patient suffering from heart failure with reduced ejection fraction, comprising:
 administering to the human patient's heart a therapeutically effective amount of an isolated BAG3 gene, BAG3 polynucleotide, BAG3 protein, BAG3 polypeptide or an expression vector comprising a BAG3 polynucleotide or cDNA sequence thereof to increase expression or amount of BAG3 polypeptides or proteins in the human patient's heart.   
     
     
         51 . The method of  claim 50 , wherein the human patient has a mutation in their BAG3 polynucleotide or polypeptide. 
     
     
         52 . The method of  claim 50 , wherein the expression vector comprises a viral vector, eukaryotic or prokaryotic plasmid, or yeast vector. 
     
     
         53 . The method of  claim 52 , wherein the viral vector comprises an adeno-associated virus vector (AAV), adenovirus vector, coxsackie virus vector, a cytomegalovirus vector, a lentivirus or retroviral vector. 
     
     
         54 . The method of  claim 53 , wherein the adeno-associated virus comprises: serotype 1 (AAV1), serotype 2 (AAV2), serotype 3 (AAV3), serotype 4 (AAV4), serotype 5 (AAV5), serotype 6 (AAV6), serotype 7 (AAV7), serotype 8 (AAV8), or serotype 9 (AAV9) capsid protein. 
     
     
         55 . The method of  claim 50 , wherein the human patient suffers from familial dilated cardiomyopathy. 
     
     
         56 . The method of  claim 50 , wherein the human patient suffers from non-familial dilated cardiomyopathy. 
     
     
         57 . The method of  claim 50 , wherein the BAG3 gene, BAG3 polynucleotide, BAG3, protein, BAG3 polypeptide or an expression vector comprising a BAG3 polynucleotide or cDNA sequence thereof is comprised in a pharmaceutical composition. 
     
     
         58 . The method of  claim 50 , wherein the expression vector comprising a BAG3 polynucleotide or cDNA sequence thereof further comprises a cardiac specific promoter. 
     
     
         59 . The method of  claim 58 , wherein the expression vector comprising the BAG3 polynucleotide or cDNA sequence that further comprises a cardiac specific promoter is flanked by one or more inverted terminal repeats (ITRs). 
     
     
         60 . The method of  claim 59 , wherein the one or more ITRs comprise AAV2 ITRs. 
     
     
         61 . The method of  claim 50 , wherein the expression vector comprising a BAG3 polynucleotide or cDNA sequence thereof further comprises a CMV promoter. 
     
     
         62 . The method of  claim 61 , wherein the expression vector comprising the BAG3 polynucleotide or cDNA sequence that further comprises a CMV promoter is flanked by one or more inverted terminal repeats (ITRs). 
     
     
         63 . The method of  claim 62 , wherein the one or more ITRs comprise AAV2 ITRs. 
     
     
         64 . The method of  claim 50 , wherein the human patient suffers from ischemic heart disease. 
     
     
         65 . The method of  claim 50 , wherein the human patient suffers from non-ischemic cardiomyopathy. 
     
     
         66 . The method of  claim 50 , wherein the BAG3 gene, BAG3 polynucleotide, BAG3 protein, BAG3 polypeptide or an expression vector comprising a BAG3 polynucleotide or cDNA sequence thereof is intravenously administered.

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