Granted Patent B2

US 12,285,479 · App. 17/389,724 · Granted Apr 29, 2025

Inventors: Eric Todd Baima (Kalamazoo, MI); Yulia Burakova (Byron Center, MI); Paul Joseph Dominowski (Kalamazoo, MI); Steven Alan Dunham (Kalamazoo, MI); Nicole Lynn Hainer (Kalamazoo, MI); John Morgan Hardham (Kalamazoo, MI); Mahesh Kumar (Portage, MI); Jason John Millership (Portage, MI); Duncan M. Mwangi (Portage, MI); Sharath K. Rai (Portage, MI); Sharon Marie Wappel (Kalamazoo, MI); Dennis Lee Foss (Mattawan, MI)

Assignee: Zoetis Services LLC

A61K39/215A61P31/14A61K2039/525A61K2039/545A61K2039/552A61K2039/55511A61K2039/55561A61K2039/55577A61K2039/55588

Abstract

Claims (13)

1. A composition comprising a protein whose amino acid sequence consists of SEQ ID NO: 17, and an adjuvant consisting of a saponin, a sterol, and a CpG-containing immunostimulatory oligonucleotide.

2. The composition according to claim 1 , wherein the Saponin is a triterpenoid saponin extracted from bark of Quillaia Saponaria and the sterol is selected from the group consisting of β-sitosterol, stigmasterol, ergosterol, ergocalciferol, and cholesterol.

3. The composition according to claim 2 , wherein the saponin is present in the amount of about 20 μg per dose and the sterol is present in the amount of about 20 μg per dose.

4. The composition according to claim 1 , wherein the immunostimulatory oligonucleotide is a P-class immunostimulatory oligonucleotide characterized by the presence of one or more TLR-9 activating motif(s) and two palindromes or two complementarity areas.

5. The composition according to claim 4 wherein said P-class immunostimulatory oligonucleotide is 5′ modified.

6. The composition according to claim 5 , wherein said P class immunostimulatory oligonucleotide comprises at least 22 contiguous nucleotides of SEQ ID NO: 8.

7. The composition according to claim 1 , wherein the CpG containing immunostimulatory oligonucleotide is present in the amount of about 20 to about 50 μg per dose.

8. A method of inducing an immune response in a subject in need thereof, the method comprising administering to said subject the composition according to claim 1 .

9. The method according to claim 8 wherein said subject is a canine.

10. The method according to claim 8 wherein said immunogenic composition is administered to said subject in a prime administration and in a boost administration, wherein the boost administration is between about 14 and about 42 days after the prime administration.

11. The method according to claim 8 wherein said immune response is a protective immune response.

12. The method according to claim 11 wherein said protective immune response is retained for at least six months after the boost administration.

13. The method according to claim 12 wherein said protective immune response is retained for at least 12 months after the boost administration.

Assignments (1)

Continuity (4)

References Cited (19)