West nile vaccine
View Patent ↗The present invention provides a safe and effective vaccine composition against West Nile virus disease. An immunogenically active component of West Nile virus or plasmid DNA, an adjuvant such as a metabolizable oil, and a pharmacologically acceptable carrier are formulated into an immunizing vaccine. The invention also provides a method for the prevention or amelioration of West Nile disease, such as encephalitis, in equidae by administering the vaccine composition herein set forth.
1. A vaccine composition against West Nile infection which comprises: an effective immunizing amount of an inactivated whole West Nile virus, an immunologically stimulating amount of a metabolizable oil and a pharmaceutically acceptable carrier, wherein said vaccine composition is effective in equidae against West Nile infection for up to twelve months and said inactivated West Nile virus is strain VM-2 having ATCC Accession No. PTA-6860 or a subculture thereof.
2. The composition according to claim 1 wherein the immunogenically active component is an inactivated whole West Nile virus, and further wherein a dosage unit of said vaccine comprises about 1×10 4 TCID 50 to about 1×10 8 TCID 50 of said virus.
3. The composition according to claim 1 wherein the metabolizable oil is SP oil.
4. The composition according to claim 2 wherein the immunogenically active component is an inactivated whole West Nile virus comprising a dosage unit of about 1×10 4 TCID 50 to about 5×10 7 TCID 50 of said virus.
5. The composition according to claim 3 wherein said oil is present in the amount of about 4% to 10% vol/vol.
6. The composition according to claim 4 wherein said virus is present in sufficient quantity to provide at least about 1×10 4 TCID 50 per unit dose of said composition.
7. The composition according to claim 5 wherein said oil is present in the amount of about 5% vol/vol.
8. The composition according to claim 7 wherein said virus is present in sufficient quantity to provide at least about 1×10 6 TCID 50 per unit dose.
9. The composition according to claim 8 wherein said virus is inactivated whole West Nile virus wherein said virus is present in sufficient quantity to provide at least about 5×10 7 TCID 50 per unit dose.
10. The composition according to claim 6 further comprising another vaccine component directed against rabies virus, Eastern equine encephalitis virus, Western equine encephalitis virus, Venezuelan equine encephalitis virus, equine herpes virus, Ehrlichia risticii, Streptococcus equi, tetanus toxoid or equine influenza virus (EIV).
11. An equine vaccine composition, comprising:
a) at least about 1×10 4 TCID 50 and up to about 1×10 9 TCID 50 per unit dose of inactivated West Nile virus wherein said inactivated West Nile virus is strain VM-2 having ATCC Accession No. PTA-6860 or a subculture thereof; and
b) about 4% to 10% vol/vol of a metabolizable oil adjuvant comprising about 1 to 3% polyoxyethylene-polyoxypropylene block copolymer, about 2 to 6% of squalene and about 0.1 to 0.5% of polyoxyethylene sorbitan monooleate.
12. West Nile virus vaccine for equidae, comprising:
a) at least about 1×10 6 TCID 50 to about 1×10 8 TCID 50 per unit dose of killed or inactivated West Nile virus wherein said killed or inactivated West Nile virus is strain VM-2 having ATCC Accession No. PTA-6860 or a subculture thereof, and
b) at least about 1% vol/vol of an adjuvant comprising at least one metabolizable oil and at least one wetting or dispersing agent.
13. The vaccine of claim 12 , wherein said vaccine comprises at least about 1×10 7 TCID 50 of said virus.
14. The vaccine of claim 13 , wherein said vaccine comprises at least about 5×10 7 TCID 50 of said virus.
15. The vaccine of claim 12 , wherein said vaccine is formulated into two dosage units.
16. The vaccine of claim 12 , comprising at least about 4% of said adjuvant.
17. The vaccine of claim 16 , comprising about 4% to 10% of said adjuvant.
18. The vaccine of claim 12 , wherein said adjuvant is SP oil.
19. The vaccine of claim 12 , comprising at least two wetting or dispersing agents.
20. The vaccine of claim 19 , wherein said wetting or dispersing agents are non-ionic surfactants.
21. The vaccine of claim 20 , wherein said non-ionic surfactants are selected from the group consisting of polyoxyethylene/polyoxypropylene block copolymers and polyoxyethylene esters.
22. A vaccine regimen for horses or other equidae, comprising two dosage units of killed or inactivated West Nile virus, wherein said killed or inactivated West Nile virus is strain VM-2 having ATCC Accession No. PTA-6860 or a subculture thereof, each said dosage unit comprises about 0.5 to 5 milliliters of a composition containing at least about 5×10 7 TCID 50 of said virus and about 1 to 10% vol/vol of an adjuvant said adjuvant comprising at least one metabolizable oil and at least two nonionic surfactants, and said dosage unit further comprises a pharmacologically acceptable carrier.
23. The vaccine regimen of claim 22 , wherein said adjuvant is SP oil.
24. The vaccine regimen of claim 23 , wherein said SP oil comprises squalane in an amount of about 2 to 6% by weight of said adjuvant, about 1 to 3% of polyoxyethylene/polyoxypropylene block copolymer by weight of said adjuvant, and about 0.1 to 0.5% of polyoxyethylene sorbitan monooleate by weight of said adjuvant.
25. The vaccine regimen of claim 22 , further comprising a vaccine component directed to at least one member selected from the group consisting of influenza virus, Eastern equine encephalitis virus, Western equine encephalitis virus, Venezuelan equine encephalitis virus, rhinopneumonitis virus and tetanus toxoid.