US2019298812A1PendingUtilityA1

Adeno-associated virus mediated gene transfer to the central nervous system

Assignee: UNIV MINNESOTAPriority: May 15, 2013Filed: Jun 11, 2019Published: Oct 3, 2019
Est. expiryMay 15, 2033(~6.8 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 3/00A61P 25/28A61P 25/00C12Y 302/01076C12N 2750/14171A61K 38/47C12N 2830/007C12N 2750/14143C12N 7/00C12N 15/86A61K 48/00H05K 999/99A61K 2039/507C12N 15/8645A61K 9/0085A61K 31/7088
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Claims

Abstract

A method to prevent, inhibit or treat one or more symptoms associated with a disease of the central nervous system by intrathecally, intracerebroventricularly or endovascularly administering a rAAV encoding a gene product associated with the disease, e.g., a mammal in which the gene product is absent or present at a reduced level relative to a mammal without the disease.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method to inhibit or treat one or more symptoms associated with a deficiency of glucocerebrosidase in a mammal, comprising:
 administering to a cisterna magna of the mammal in need thereof a composition comprising an amount of a recombinant adeno-associated virus (rAAV) 9 or rAAVrh10 vector comprising an open reading frame encoding glucocerebrosidase effective to inhibit or treat the one or more symptoms associated with the deficiency.   
     
     
         2 . The method of  claim 1 , wherein the mammal has Gaucher disease. 
     
     
         3 . The method of  claim 1 , wherein the mammal has Parkinson disease. 
     
     
         4 . The method of  claim 1 , wherein the mammal is an immunocompetent adult. 
     
     
         5 . The method of  claim 1 , wherein the mammal is a human. 
     
     
         6 . The method of any one of  claims 1 , wherein prior to administration of the composition the mammal is immunotolerized to glucocerebrosidase. 
     
     
         7 . The method of  claim 1  wherein rAAV9 vector is administered. The method of  claim 1 , wherein rAAVrh10 vector is administered. 
     
     
         9 . The method of  claim 1 , further comprising administering to the mammal in need thereof an immune suppressant. 
     
     
         10 . The method of  claim 9 , wherein the immune suppressant comprises cyclophosphamide, a glucocorticoid, cytostatic agents including an alkylating agent, an anti-metabolite, a cytotoxic antibiotic, an antibody, an agent active on immunophilin, a nitrogen mustard, nitrosourea, platinum compound, methotrexate, azathioprine, mercaptopurine, fluorouracil, dactinomycin, an anthracycline, mitomycin C, bleomycin, mithramycin, IL-2 receptor-(CD25-) or CD3-directed antibodies, anti-IL-2 antibodies, ciclosporin, tacrolimus, sirolimus, IFN-beta, IFN-gamma, an opioid, or a TNF-alpha (tumor ecrosis factor-alpha) binding agent. 
     
     
         11 . The method of  claim 9 , wherein the rAAV vector and the immune suppressant are co-administered or the immune suppressant is administered after the rAAV vector. 
     
     
         12 . The method of  claim 9 , wherein the rAAV vector is a rAAV-9 vector. 
     
     
         13 . The method of  claim 9  wherein the rAAV vector is rAAVrh10 vector. 
     
     
         14 . The method of  claim 9 , wherein the immune suppressant is administered before: rAAV9 or rAAVh10 vector. 
     
     
         15 . The method of  claim 9 , wherein the immune suppressant is systemically administered. 
     
     
         16 . The method of  claim 9 , wherein the mammal is a human.

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