IP Library Granted Patent US 9,480,739
Granted Patent B2
US 9,480,739 · App. 14/202,454 · Granted Nov 1, 2016

Bovine virus vaccines that are liquid stable

Inventors: Brad Eddy (Omaha, NE); Zhisong Qiao (Omaha, NE); Kevin O'Connell (Omaha, NE)
Assignee: Intervet Inc.
A61K39/39A61K39/02A61K39/0208A61K39/102A61K39/12A61K39/155A61K39/215A61K39/245A61K39/265A61K47/183A61K47/26C12N7/00A61K2039/5254A61K2039/552A61K2039/55583A61K2039/70C12N2710/16734C12N2760/12234C12N2760/18034C12N2760/18634C12N2770/20034C12N2770/24333C12N2770/24334
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Quick Facts
Patent No.
US 9,480,739
App. No.
14/202,454
Granted
Nov 1, 2016
Kind
B2
Abstract

The present invention discloses liquid stable bovine vaccines that comprise a live attenuated virus, and a sugar alcohol. The present invention also discloses the manufacture of such vaccines and methods of protecting an animal by administration of such vaccines.

Claims (22)

1. A liquid stable vaccine that comprises a live attenuated bovine virus, a 5-40% (w/v) sugar alcohol, and 0.15 to 0.75 M of an amino acid selected from the group consisting of arginine, glutamic acid, and glycine; wherein the liquid stable vaccine has a pH of 6.0 to 8.0; and

wherein the live attenuated bovine virus is selected from the group consisting of a bovine viral diarrhea virus (BVDV), an infectious bovine rinotracheitis virus (IBR), a parainfluenza type 3 virus (PI3), a bovine respiratory syncytial virus (BRSV), and any combination thereof.

2. The liquid stable vaccine of claim 1 wherein the sugar alcohol is sorbitol.

3. The liquid stable vaccine of claim 2 wherein the amino acid is arginine.

4. The liquid stable vaccine of claim 1 further comprising a sugar additive that is a non-sugar alcohol, wherein the total amount of the sugar alcohol and the non-sugar alcohol in the liquid stable vaccine is 10-40% (w/v).

5. The liquid stable vaccine of claim 1 wherein the non-sugar alcohol is selected form the group consisting of sucrose and trehalose.

6. The liquid stable vaccine of claim 1 that further comprises a component selected from the group consisting of an antioxidant, a surfactant, and a chelator.

7. The liquid stable vaccine of claim 1 that further comprises a buffer.

8. The liquid stable vaccine of claim 7 wherein the buffer comprises 2.5 to 50 mM potassium phosphate.

9. The liquid stable vaccine of claim 1 , wherein the amino acid is arginine.

10. The liquid stable vaccine of claim 3 , wherein the live attenuated virus is a BVDV selected from the group consisting of BVDV1, BVDV2, and BVDV1 and BVDV2.

11. The liquid stable vaccine of claim 10 that further comprises a live attenuated IBR.

12. The liquid stable vaccine of claim 11 that further comprises a live attenuated PI3.

13. The liquid stable vaccine of claim 12 that further comprises a live attenuated BRSV.

14. The liquid stable vaccine of claim 13 that further comprises a killed bovine virus.

15. The liquid stable vaccine of claim 13 that further comprises a bacterium.

16. The liquid stable vaccine of claim 15 wherein the bacterium is selected from the group consisting of a live attenuated or killed Pasteurella multocida, Mannheimia haemolytica, Histophilus somni, Mycoplasma bovis , and any combination thereof.

17. A method of vaccinating a bovine against bovine viral diarrhea virus (BVDV), infectious bovine rinotracheitis (IBR) virus, parainfluenza type 3 (PI3), and bovine respiratory syncytial virus (BRSV) comprising administering to the bovine the liquid stable vaccine of claim 13 .

18. A method of vaccinating a bovine against a bovine virus comprising administering to the bovine the liquid stable vaccine of claim 1 .

19. A method of making a liquid stable bovine vaccine that comprises combining a therapeutically effective amount of a live attenuated bovine virus with a 5-40% (w/v) sugar alcohol, 0.15 to 0.75 M arginine; wherein the live attenuated bovine virus is selected from the group consisting of a bovine viral diarrhea virus (BVDV), an infectious bovine rinotracheitis virus (IBR), a parainfluenza type 3 virus (PI3), a bovine respiratory syncytial virus (BRSV), and any combination thereof; and

wherein the liquid stable vaccine has a pH of 6.0 to 8.0.

20. The liquid stable vaccine of claim 2 , wherein the live attenuated virus is a BVDV selected from the group consisting of BVDV1, BVDV2, and BVDV1 and BVDV2.

Assignments (2)
CHANGE OF ADDRESS Recorded Sep 26, 2023
From: INTERVET INC.
To: INTERVET INC.
Reel/Frame 065028/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2014
From: EDDY, BRAD; QIAO, ZHISONG; O'CONNELL, KEVIN
To: INTERVET INC.
Reel/Frame 033578/0449 →
Continuity (2)
Provisional Application 61788982 · Mar 15, 2013
Related Publication 20140271709A1 · Sep 18, 2014