Methods and compositions for the treatment of defects in lipoprotein metabolism
View Patent ↗The invention provides a recombinant viral vector comprising the DNA of, or corresponding to, at least a portion of the genome of an adenovirus, which portion is capable of infecting a hepatic cell; and a human VLDL receptor gene operatively linked to regulatory sequences directing its expression. The vector is capable of expressing the normal VLDL receptor gene product in hepatic cells in vivo or in vitro. This viral vector is useful in the treatment of metabolic disorders caused by the accumulation of LDL in plasma, such as familial hypercholesterolemia or familial combined hyperlipidemia.
1. A recombinant adenoviral vector comprising AAV 5′ and 3′ ITRs flanking a human very low density lipoprotein (VLDL) receptor minigene sequence comprising a CMV promoter operatively linked to the nucleic acid sequence encoding the human VLDL receptor.
2. The vector according to claim 1 , wherein said human VLDL receptor has the amino acid sequence of SEQ ID NO: 2.
3. The vector according to claim 1 , wherein said nucleic acid sequence encoding a human VLDL receptor has the nucleotide sequence of SEQ ID NO: 1.
4. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the recombinant viral vector of claim 1 , wherein said vector is present in an amount effective to lower plasma cholesterol levels when administered in vivo to an individual.
5. The composition according to claim 4 , wherein said human VLDL receptor has the amino acid sequence of SEQ ID NO: 2.
6. The composition according to claim 4 , wherein said nucleic acid sequence encoding a human VLDL receptor has the nucleotide sequence of SEQ ID NO: 1.
7. A method of lowering plasma cholesterol levels comprising the step of administering the pharmaceutical composition according to claim 4 to an individual.
8. The recombinant vector according to claim 1 , wherein said vector comprises further AAV sequences that have a deletion in the AAV rep and/or AAV cap genes.
9. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the recombinant vector of claim 8 , wherein said vector is present in an amount effective to lower plasma cholesterol levels when administered in vivo to an individual.
10. A method of lowering plasma cholesterol levels comprising the step of administering the pharmaceutical composition according to claim 9 to an individual.