Antisense antiviral compounds and methods for treating a filovirus infection
View Patent ↗The present invention provides antisense antiviral compounds, compositions, and methods of their use and production, mainly for inhibiting the replication of viruses of the Filoviridae family, including Ebola and Marburg viruses. The compounds, compositions, and methods also relate to the treatment of viral infections in mammals including primates by Ebola and Marburg viruses. The antisense antiviral compounds include phosphorodiamidate morpholino oligonucleotides (PMOplus) having a nuclease resistant backbone, about 15-40 nucleotide bases, at least two but typically no more than half piperazine-containing intersubunit linkages, and a targeting sequence that is targeted against the AUG start site region of Ebola virus VP35, Ebola virus VP24, Marburg virus VP24, or Marburg virus NP, including combinations and mixtures thereof.
1. A morpholino antisense oligonucleotide of 23 bases comprising the base sequence of SEQ ID NO:79, wherein the morpholino antisense oligonucleotide is linked to a polyethylene glycol moiety.
2. The morpholino antisense oligonucleotide of claim 1 , wherein the morpholino antisense oligonucleotide is a phosphorodiamidate oligonucleotide.
3. The morpholino antisense oligonucleotide of claim 1 , wherein at least two to no more than half of the total number of phosphorus-containing intersubunit linkages are positively charged.
4. The morpholino antisense oligonucleotide of claim 3 , wherein the morpholino antisense oligonucleotide comprises positively charged phosphorus-containing intersubunit linkages between bases 10 and 11, bases 12 and 13, bases 14 and 15, bases 18 and 19, and bases 19 and 20 of SEQ ID NO:79.
5. The morpholino antisense oligonucleotide of claim 1 , comprising phosphorus-containing intersubunit linkages in accordance with the structure:
wherein P j and P i are purine or pyrimidine base-pairing moieties effective to bind, by base-specific hydrogen bonding, to a base in a polynucleotide; and
X is fluoro, alkyl, alkoxy, thioalkoxy, alkyl amino, a cyclic amine, 4-morpholine, 1-piperidine, 1-piperazine, or —NR 2 , wherein each R is independently H or lower alkyl;
Y 1 is O; and
Z is O.
6. The morpholino antisense oligonucleotide of claim 5 , wherein X is NH 2 , NHR or NR 2 , wherein each R is a lower alkyl.
7. The morpholino antisense oligonucleotide of claim 6 , wherein X is N(CH 3 ) 2 .
8. The morpholino antisense oligonucleotide of claim 5 , wherein X is 1-piperazine for two to no more than half of the total number of phosphorus-containing intersubunit linkages.
9. The morpholino antisense oligonucleotide of claim 5 , wherein X is 1-piperazine at phosphorus-containing intersubunit linkages between bases 10 and 11, bases 12 and 13, bases 14 and 15, bases 18 and 19, and bases 19 and 20 of SEQ ID NO:79, and X is N(CH 3 ) 2 for the remaining phosphorus-containing intersubunit linkages.
10. A pharmaceutical composition, comprising a morpholino antisense oligonucleotide of 23 bases comprising the base sequence of SEQ ID NO:79, wherein the morpholino antisense oligonucleotide is linked to a polyethylene glycol moiety, and a pharmaceutically acceptable carrier.
11. The pharmaceutical composition of claim 10 , wherein the morpholino antisense oligonucleotide is a phosphorodiamidate oligonucleotide.
12. The pharmaceutical composition of claim 10 , wherein at least two to no more than half of the total number of phosphorus-containing intersubunit linkages are positively charged.
13. The pharmaceutical composition of claim 10 , wherein the morpholino antisense oligonucleotide comprises positively charged phosphorus-containing intersubunit linkages between bases 10 and 11, bases 12 and 13, bases 14 and 15, bases 18 and 19, and bases 19 and 20 of SEQ ID NO:79.
14. The pharmaceutical composition of claim 10 , comprising phosphorus-containing intersubunit linkages in accordance with the structure:
wherein P j and P i are purine or pyrimidine base-pairing moieties effective to bind, by base-specific hydrogen bonding, to a base in a polynucleotide; and
X is fluoro, alkyl, alkoxy, thioalkoxy, alkyl amino, a cyclic amine, 4-morpholine, 1-piperidine, 1-piperazine, or —NR 2 , wherein each R is independently H or lower alkyl;
Y 1 is O; and
Z is O.
15. The pharmaceutical composition of claim 14 , wherein X is 1-piperazine at phosphorus-containing intersubunit linkages between bases 10 and 11, bases 12 and 13, bases 14 and 15, bases 18 and 19, and bases 19 and 20 of SEQ ID NO:79, and X is N(CH 3 ) 2 for the remaining phosphorus-containing intersubunit linkages.
16. A morpholino antisense oligonucleotide of 23 bases comprising the base sequence of SEQ ID NO:79, wherein the morpholino antisense oligonucleotide comprises a formula:
and wherein the morpholino antisense oligonucleotide is linked to a polyethylene glycol moiety.
17. A pharmaceutical composition, comprising a morpholino antisense oligonucleotide of 23 bases comprising the base sequence of SEQ ID NO:79, wherein the morpholino antisense oligonucleotide comprises a formula:
and wherein the morpholino antisense oligonucleotide is linked to a polyethylene glycol moiety, and a pharmaceutically acceptable carrier.