Anti-flavivirus compounds and methods of use
The present invention concerns the use of compounds and compositions for the treatment or prevention of Flavivirus infections, such as dengue virus infections and Zika virus infections. Aspects of the invention include methods for treating or preventing Flavivirus virus infection, such as dengue virus and Zika virus infection, by administering a compound or composition of the invention, to a subject in need thereof; methods for inhibiting Flavivirus infections, such as dengue virus and Zika virus infections, in a cell in vitro or in vivo; pharmaceutical compositions; packaged dosage formulations; and kits useful for treating or preventing Flavivirus infections, such as dengue virus and Zika virus infections.
1. A method for treating a Flavivirus infection in a human or non-human mammalian subject, said method comprising administering an effective amount of a compound to the subject having the Flavivirus infection, wherein the compound is colchicine, a prodrug of colchicine, a metabolite of colchicine, or a pharmaceutically acceptable salt of any of the foregoing, and wherein the Flavivirus infection is dengue virus infection or Zika virus infection.
2. The method of claim 1 , wherein the Flavivirus infection is dengue virus infection.
3. The method of claim 1 , wherein the compound is administered to the subject orally, nasally, rectally, parenterally, subcutaneously, intramuscularly, or intravascularly.
4. The method of claim 1 , further comprising administering an additional agent to the subject, for treating the Flavivirus infection, or a symptom thereof, in the same formulation as the compound, or in a separate formulation before, during, or after administration of the compound.
5. The method of claim 1 , wherein the compound is administered to the subject in a pharmaceutical composition that further comprises a pharmaceutically acceptable carrier or diluent.
6. The method of claim 1 , wherein the Flavivirus infection is Zika virus infection.
7. The method of claim 1 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof.
8. The method of claim 1 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, and wherein the Flavivirus infection is dengue virus infection.
9. The method of claim 1 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, and wherein the Flavivirus infection is Zika virus infection.
10. The method of claim 1 , wherein the subject is human, wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, and wherein the Flavivirus infection is dengue virus infection.
11. The method of claim 1 , wherein the subject is human, wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, and wherein the Flavivirus infection is Zika virus infection.
12. A method for inhibiting Flavivirus infection in human or non-human mammalian cells in vitro or in vivo, said method comprising contacting an effective amount of a compound to the human or non-human mammalian cell in vitro or in vivo after exposure of the cell to the Flavivirus, wherein the compound is colchicine, a prodrug of colchicine, a metabolite of colchicine, or a pharmaceutically acceptable salt of any of the foregoing, wherein the Flavivirus is dengue virus or Zika virus, and wherein the Flavivirus infection is dengue virus infection or Zika virus infection.
13. The method of claim 12 , wherein the Flavivirus is dengue virus, and wherein the Flavivirus infection is dengue virus infection.
14. The method of claim 12 , wherein the Flavivirus is Zika virus, and wherein the Flavivirus infection is Zika virus infection.
15. The method of claim 12 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof.
16. The method of claim 12 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, wherein the Flavivirus is dengue virus, and wherein the Flavivirus infection is dengue virus infection.
17. The method of claim 12 , wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, wherein the Flavivirus is Zika virus, and wherein the Flavivirus infection is Zika virus infection.
18. The method of claim 12 , wherein the cell is a human cell, wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, wherein the Flavivirus is dengue virus, and wherein the Flavivirus infection is dengue virus infection.
19. The method of claim 12 , wherein the cell is a human cell, wherein the compound is colchicine or a pharmaceutically acceptable salt thereof, wherein the Flavivirus is Zika virus, and wherein the Flavivirus infection is Zika virus infection.