Therapeutic strategies to treat CNS pathology in mucopolysaccharidoses
The invention provides for nucleotide sequences encoding for a chimeric sulfatase, viral vectors expressing such sequences for gene therapy and pharmaceutical uses of the chimeric expressed protein. The invention is particularly applied in the therapy of mucopolysaccharidosis, preferably type IIIA.
1. A nucleotide sequence encoding for a chimeric sulfatase, wherein the encoded chimeric sulfatase consists essentially of, in the N-terminal to C-terminal sequence order:
a) a signal peptide derived from either the human α-antitrypsin (hAAT) amino acid sequence or the human Iduronate-2-sulfatase (IDS) amino acid sequence;
b) a human sulfatase derived amino acid sequence that is deprived of its signal peptide; and
c) an ApoB LDLR-binding domain.
2. The nucleotide sequence according to claim 1 , wherein the encoded signal peptide has the sequence of SEQ ID NO: 2 or SEQ ID NO: 4.
3. The nucleotide sequence according to claim 1 , wherein the encoded human sulfatase derived amino acid sequence of b), is derived from human sulfamidase.
4. The nucleotide sequence according to claim 3 , wherein the encoded human sulfamidase derived amino acid sequence consists essentially of the sequence of SEQ ID NO: 8.
5. The nucleotide sequence according to claim 1 , wherein the encoded ApoB LDLR-binding domain consists essentially of the sequence of SEQ ID NO: 10.
6. The nucleotide sequence according to claim 1 , wherein the nucleotide sequence is selected from the group consisting of:
a) Assembly hAATsp-SGSH-3xflag-ApoB cassette (SEQ ID NO: 15),
b) Assembly hIDSsp-SGSH-3xflag-ApoB cassette (SEQ ID NO: 17),
c) Assembly hAATsp-SGSH-ApoB cassette (SEQ ID NO: 23), and
d) Assembly hIDSsp-SGSH-ApoB cassette (SEQ ID NO: 25).
7. A recombinant plasmid comprising the nucleotide sequence according to claim 1 , under the control of a liver specific promoter.
8. The recombinant plasmid according to claim 7 , wherein the liver specific promoter is the human thyroid hormone-globulin (TBG) promoter.
9. The recombinant plasmid according to claim 8 , wherein the human thyroid hormone-globulin (TBG) promoter consists essentially of SEQ ID NO: 27.
10. The recombinant plasmid according to claim 7 , that is able to be assembled into a viral vector, wherein the viral vector is selected from the group consisting of lentiviral vectors, helper-dependent adenoviral vectors, and AAV vectors.
11. The recombinant plasmid according to claim 10 , that is recombinant plasmid AAV2.1.
12. A viral vector comprising the recombinant plasmid according to claim 7 .
13. The viral vector according to claim 12 , that is an AAV viral vector.
14. The viral vector according to claim 13 , that is an AAV serotype 8 vector.
15. A pharmaceutical composition comprising the viral vector according to claim 12 .
16. A chimeric sulfatase encoded by the nucleotide sequence of claim 1 .
17. The chimeric sulfatase according to claim 16 , wherein the human sulfatase that is encoded by b) is derived from human sulfamidase.
18. The chimeric sulfatase according to claim 17 , wherein the human sulfatase that is derived from human sulfamidase consists essentially of SEQ ID NO: 8.
19. The chimeric sulfatase according to claim 16 , wherein the encoded ApoB LDLR-binding domain consists essentially of SEQ ID NO: 10.
20. The chimeric sulfatase according to claim 16 , that has an amino acid sequence selected from the group consisting of:
a) hAATsp-SGSH-3xflag-ApoB amino acid sequence (SEQ ID NO: 16),
b) hIDSsp-SGSH-3xflag-ApoB amino acid sequence (SEQ ID NO: 18),
c) hAATsp-SGSH-ApoB amino acid sequence (SEQ ID NO: 24), and
d) hIDSsp-SGSH-ApoB amino acid sequence (SEQ ID NO: 26).
21. A pharmaceutical composition comprising the chimeric sulfatase according to claim 16 , and suitable diluents and/or excipients and/or carriers.