IP Library Granted Patent US 8,821,852
Granted Patent B2
US 8,821,852 · App. 13/995,740 · Granted Sep 2, 2014

Vaccines with live bacterial isolates for systemic administration

Inventors: Kevin A. O'Connell (Omaha, NE); Rhonda LaFleur (Omaha, NE); Huchappa Gowda Jayappa (Omaha, NE); Terri L. Wasmoen (Omaha, NE)
Assignee: Intervet Inc.
A61K39/099A61K2039/70A61K2039/552A61K2039/5252A61K39/12A61K2039/5254A61K2039/55505C12N2760/16134C12N2760/18734A61K2039/521A61K2039/522
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Quick Facts
Patent No.
US 8,821,852
App. No.
13/995,740
Granted
Sep 2, 2014
Kind
B2
Abstract

The present invention pertains to vaccines suitable for administering systemically that comprise live aro mutant bacteria, an adjuvant, an aromatic supplement, or both an adjuvant and an aromatic supplement. The present invention also pertains to the manufacture of such a vaccine and a method of protecting an animal by administration of the vaccine.

Claims (23)

1. A vaccine for protecting an animal against a clinical disease arising from an infection with Bordetella bronchiseptica ( B. bronchiseptica ) comprising a live aro mutant B. bronchiseptica strain and an aromatic supplement; wherein the vaccine is suitable for systemic administration.

2. The vaccine of claim 1 wherein the aromatic supplement comprises tyrosine, tryptophan, and phenylalanine.

3. The vaccine of claim 2 wherein the aromatic supplement further comprises para-aminobenzoic acid.

4. The vaccine of claim 3 wherein the aromatic supplement further comprises 2,3-dihydroxybenzoic acid.

5. The vaccine of claim 1 wherein the live aro mutant B. bronchiseptica strain is a live aroA mutant B. bronchiseptica strain.

6. The vaccine of claim 5 that further comprises an adjuvant.

7. The vaccine of claim 6 wherein the adjuvant comprises an aluminum salt.

8. The vaccine of claim 7 wherein the aluminium salt is selected from the group consisting of aluminum phosphate, aluminum potassium sulfate, and aluminum hydroxide.

9. The vaccine of claim 8 , that further comprises a canine influenza virus antigen, a canine parainfluenza virus antigen, or both a canine influenza virus antigen and a canine parainfluenza virus antigen.

10. The vaccine of claim 9 wherein the aromatic supplement comprises tyrosine, tryptophan, and phenylalanine.

11. The vaccine of claim 10 wherein the aromatic supplement further comprises para-aminobenzoic acid and 2,3-dihydroxybenzoic acid.

12. The vaccine of claim 5 , that further comprises a canine influenza virus antigen, a canine parainfluenza virus antigen, or both a canine influenza virus antigen and a canine parainfluenza virus antigen.

13. The vaccine of claim 12 wherein the canine influenza virus antigen is a killed canine influenza virus and the canine parainfluenza virus antigen is a modified live canine parainfluenza virus.

14. The vaccine of claim 13 , wherein the live aroA mutant B. bronchiseptica strain and the modified live canine parainfluenza virus are in freeze-dried spheres and the killed canine influenza virus is in a diluent.

15. A vaccine for protecting an animal against a clinical disease arising from an infection with Bordetella bronchiseptica ( B. bronchiseptica ) comprising a live aro mutant B. bronchiseptica strain and an adjuvant; wherein the vaccine is suitable for systemic administration; and wherein the adjuvant comprises an aluminium salt selected from the group consisting of aluminum phosphate, aluminum potassium sulfate, aluminum hydroxide, and a combination thereof; and wherein the amount of the aluminium salt in the vaccine is between 0.5 to 15%.

16. The vaccine of claim 15 , wherein the aluminium salt in the vaccine is between 1.5 to 7.5% aluminum hydroxide.

17. A multivalent vaccine comprising a live aro mutant Bordetella bronchiseptica ( B. bronchiseptica ) strain that comprises a nucleic acid encoding canine influenza virus H3 hemagglutinin protein; wherein said nucleic acid is operably linked to a promoter; and whereby said live aro mutant B. bronchiseptica strain can express the canine influenza virus H3 hemagglutinin.

18. The multivalent vaccine of claim 17 , wherein the multivalent vaccine further comprises an aromatic supplement.

19. A method of aiding in the protection of a canine against a clinical disease arising from an infection with B. bronchiseptica comprising administering systemically the vaccine of claim 11 to that canine.

20. A method of aiding in the protection of an animal against a clinical disease arising from an infection with B. bronchiseptica comprising administering systemically the vaccine of claim 1 to that animal.

21. An immunogenic composition comprising a live aro mutant Bordetella bronchiseptica ( B. bronchiseptica ) strain that comprises a nucleic acid encoding an antigenic fragment of canine influenza virus H3 hemagglutinin protein; wherein said nucleic acid is operably linked to a promoter; and whereby said live aro mutant B. bronchiseptica strain can express the antigenic fragment of canine influenza virus H3 hemagglutinin protein.

22. The immunogenic composition of claim 21 , wherein the immunogenic composition further comprises an aromatic supplement.

23. The vaccine of claim 2 , wherein the amount of tyrosine is between 4 μg/mL and 0.4 mg/mL, the amount of tryptophan is between 4 μg/mL and 0.4 mg/mL, and the amount of phenylalanine is between 4 μg/mL and 0.4 mg/mL.

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 Jan 13, 2014
From: O'CONNELL, KEVIN A.; LAFLEUR, RHONDA; JAYAPPA, HUCHAPPA GOWDA; WASMOEN, TERRI L.
To: INTERVET INC.
Reel/Frame 031952/0237 →
Priority Claims (1)
EP 11152829 · Feb 1, 2011 · regional
Continuity (3)
Provisional Application 61556975 · Nov 8, 2011
Provisional Application 61425855 · Dec 22, 2010
Related Publication 20130273100A1 · Oct 17, 2013