US2013323207A1PendingUtilityA1

Products and methods for delivery of polynucleotides by adeno-associated virus for lysosomal storage disorders

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Assignee: NATIONWIDE CHILDRENS HOSPITALPriority: Jun 8, 2011Filed: Jun 20, 2013Published: Dec 5, 2013
Est. expiryJun 8, 2031(~4.9 yrs left)· nominal 20-yr term from priority
A61P 3/00C12N 15/86C12N 2750/14171A61K 48/005A61K 35/761C12Y 310/01001C12N 9/14C12N 2750/14143A61K 38/46C12N 2750/14121C12N 7/00A61K 47/26
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Claims

Abstract

The present invention relates to methods and materials useful for systemically delivering polynucleotides across the blood brain barrier using adeno-associated virus as a vector. For example, the present invention relates to methods and materials useful for systemically delivering α-N-acetylglucosamidinase polynucleotides to the central and peripheral nervous systems, as well as the somatic system. Use of these methods and materials is indicated, for example, for treatment of the lysosomal storage disorder mucopolysaccharidosis IIIB. As another example, the present invention relates to methods and materials useful for systemically delivering N-sulphoglucosamine sulfphohydrolase polynucleotides to the central and peripheral nervous systems, as well as the somatic system. Use of this second type of methods and materials is indicated, for example, for treatment of the lysosomal storage disorder mucopolysaccharidosis IIIA.

Claims

exact text as granted — not AI-modified
1 - 17 . (canceled) 
     
     
         18 . A method of delivering an N-sulphoglucosamine sulphohydrolase polynucleotide to the central nervous system comprising the step of systemically administering a rAAV9 or rh74 comprising a self-complementary genome including the polynucleotide to a patient. 
     
     
         19 - 26 . (canceled) 
     
     
         27 . A method of treating mucopolysaccharidosis IIIA comprising the step of systemically administering a rAAV9 or rh74 comprising a self-complementary genome including an N-sulphoglucosamine sulphohydrolase polynucleotide to a patient. 
     
     
         28 - 31 . (canceled) 
     
     
         32 . The method of  claim 18  wherein mannitol is administered prior to the administration of the rAAV. 
     
     
         33 . The method of  claim 27  wherein mannitol is administered prior to the administration of the rAAV. 
     
     
         34 . The method of  claim 18  wherein the sequence of the N-sulphoglucosamine sulphohydrolase polynucleotide is set out in SEQ ID NO: 3. 
     
     
         35 . The method of  claim 27  wherein the sequence of the N-sulphoglucosamine sulphohydrolase polynucleotide is set out in SEQ ID NO: 3. 
     
     
         36 . The method of  claim 32  wherein the sequence of the N-sulphoglucosamine sulphohydrolase polynucleotide is set out in SEQ ID NO: 3. 
     
     
         37 . The method of  claim 33  wherein the sequence of the N-sulphoglucosamine sulphohydrolase polynucleotide is set out in SEQ ID NO: 3.

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