Methods and compositions for modulating sialic acid production and treating hereditary inclusion body myopathy
According to certain embodiments of the present invention, methods for modulating the production of sialic acid in a system are provided, which comprise providing the system with a wild-type GNE-encoding nucleic acid sequence. According to such embodiments, the system may comprise a cell, muscular tissue, or other desirable targets. Similarly, the present invention encompasses methods for producing wild-type GNE in a system that comprises a mutated endogenous GNE-encoding sequence. In other words, the present invention includes providing, for example, a cell or muscular tissue that harbors a mutated (defective) GNE-encoding sequence with a functional wild-type GNE encoding sequence.
1. A method for modulating the production of sialic acid in a human, which comprises the steps of :
providing a human subject in need of treatment of a hereditary inclusion body myopathy;
providing a vector comprising a liposome or a lipid nanoparticle and a human wild-type GNE-encoding nucleic acid sequence, wherein the wild-type GNE-encoding nucleic acid sequence that comprises SEQ ID NO: 9; and
providing the vector by intramuscular administration in an amount sufficient to ameliorate the effects of the hereditary inclusion body myopathy local to the site of intramuscular administration in human muscle tissue.
2. The method of claim 1 , wherein the wild-type GNE-encoding nucleic acid sequence comprises a promoter operably connected to the wild-type GNE-encoding nucleic acid sequence.
3. The method of claim 2 , wherein the promoter is the CMV promoter.
4. The method of claim 2 , wherein the wild-type GNE-encoding nucleic acid sequence is disposed within or is connected to a lipid nanoparticle.
5. The method of claim 4 , wherein the lipid nanoparticle comprises one or more agents capable of recognizing and binding to a muscle cell or a component thereof.
6. A method for expressing a wild-type GNE in a human with a mutant GNE, wherein the method comprises injecting a the wild-type GNE-encoding sequence within a liposome or lipid nanoparticle that is injected via intramuscular administration at a location in a muscle with hereditary inclusion body myopathy, wherein the wild type GNE-encoding nucleic acid sequence comprises SEQ ID NO: 9.
7. The method of claim 6 , wherein the wild-type GNE-encoding nucleic acid sequence comprises a promoter operably connected to the wild-type GNE-encoding nucleic acid sequence.
8. The method of claim 7 , wherein the promoter is the CMV promoter.
9. The method of claim 6 , wherein the lipid nanoparticle comprises one or more agents capable of recognizing and binding to a muscle cell or a component thereof.
10. A method for ameliorating the effects of Hereditary Inclusion Body Myopathy, which comprises the steps of:
identifying a human patient with Hereditary Inclusion Body Myopathy; and
providing a patient with an effective amount of a wild-type GNE-encoding nucleic acid sequence by intramuscular administration at a location with Hereditary Inclusion Body Myopathy, wherein the wild-type GNE-encoding nucleic acid sequence comprises SEQ ID NO: 9 in a liposome or a lipid nanoparticle to ameliorate the effects of the Hereditary Inclusion Body Myopathy in human muscle cells.
11. The method of claim 10 , wherein the wild-type GNE-encoding nucleic acid sequence comprises a promoter operably connected to the wild-type GNE-encoding nucleic acid sequence.
12. The method of claim 11 , wherein the promoter is the CMV promoter.
13. The method of claim 11 , wherein the wild-type GNE-encoding nucleic acid sequence is disposed within or is connected to a lipid nanoparticle.
14. The method of claim 13 , wherein the lipid nanoparticle comprises one or more agents capable of recognizing and binding to a muscle cell or a component thereof.