IP Library Granted Patent US 10,967,058
Granted Patent B2
US 10,967,058 · App. 16/374,105 · Granted Apr 6, 2021

Foot-and-mouth disease vaccine

Inventors: Paul Joseph Dominowski (Kalamazoo, MI); John Morgan Hardham (Kalamazoo, MI); James Alan Jackson (Kalamazoo, MI); Cyril Gerard Gay (Bethesda, MD); Luis Leandro Rodriguez (Niantic, CT); Peter William Krug (East Setauket, NY); Aida Elizabeth Rieder (Westbrook, CT)
Assignees: Zoetis Services LLC; United States of America, as represented by the Secretary of Agriculture
A61K39/135A61K39/12A61K39/39A61K2039/5252A61K2039/552A61K2039/555A61K2039/55505A61K2039/55511A61K2039/55561A61K2039/55566A61K2039/55583C12N2770/32034C12N2770/32134
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Quick Facts
Patent No.
US 10,967,058
App. No.
16/374,105
Granted
Apr 6, 2021
Kind
B2
Abstract

Compositions for prevention of Foot and Mouth Disease (FMD) are provided, comprising an antigen component in the amount equivalent to 0.5-20 μg FMD virus and an adjuvant component comprising oil, an immunostimulatory oligonucleotide, and a polycationic carrier. Methods of using the composition, as well as the methods of reducing FMD persistence are also provided.

Claims (30)

1. An immunogenic composition comprising an antigen component and an adjuvant component, wherein

a) the adjuvant component comprises an emulsion containing oil, an immunostimulatory oligonucleotide, and diethylaminoethyl (DEAE) Dextran and

b) the antigen component comprises 0.5-10 μg or 6-20 μg of FMD (Foot-and-Mouth Disease) virus composition per dose.

2. The immunogenic composition of claim 1 , wherein the immunostimulatory oligonucleotide comprises CpG.

3. The immunogenic composition of claim 1 , wherein the immunostimulatory oligonucleotide comprises at least 15 contiguous nucleotides of SEQ ID NO: 8.

4. The immunogenic composition of claim 1 , wherein said oily phase is present in the amount of up to 80% v/v of the composition.

5. The immunogenic composition of claim 1 , wherein the oily phase comprises 50.01%-55% v/v of the composition.

6. The immunogenic composition of claim 1 , wherein the adjuvant component comprises SEQ ID NO: 8 and diethylaminoethyl (DEAE) Dextran.

7. The immunogenic composition of claim 6 , wherein the DEAE Dextran is present in the amount of 6-200 mg per dose.

8. The immunogenic composition of claim 7 , wherein the immunostimulatory oligonucleotide is present in the amount of 6-200 μg per dose.

9. The immunogenic composition of claim 1 , wherein said FMD virus composition is a preparation of FMD virus Cruzeiro strain.

10. The immunogenic composition of claim 9 , wherein said FM D virus Cruzeiro strain is genetically engineered.

11. The immunogenic composition of claim 10 , wherein said FMD virus Cruzeiro strain contains a deletion of the leader coding region (LL).

12. The immunogenic composition of claim 11 , wherein said FMD virus Cruzeiro strain contains negative antigenic markers introduced in one or both of the viral non-structural 3DP pol and 3B proteins.

13. The immunogenic composition of claim 10 , wherein said FMD virus Cruzeiro strain contains a heterologous capsid protein.

14. The immunogenic composition of claim 13 , wherein the heterologous capsid protein is from a strain selected from Asia1, Turkey06, O1Campos, C3Indaial, and A2001-Argentina.

15. An immunogenic composition according to claim 13 , comprising DEAE Dextran in the amount of 6-200 mg per dose, and the immunostimulatory oligonucleotide comprising at least 15 contiguous nucleotides of SEQ ID NO: 8 is present in the amount of 6-200 μg per dose.

16. A method of preventing FMD in an animal in need thereof, comprising administering to said animal the immunogenic composition according to claim 15 .

17. The immunogenic composition of claim 1 , wherein the antigen component comprises

a) 0.5-6 μg of FMD virus per dose; or

b) 0.5-4 μg of FMD virus per dose; or

c) 0.5-2 μg of FMD virus per dose; or

d) 0.5-1.5 μg of FMD virus per dose; or

e) 6-20 μg of FMD virus per dose; or

f) 6-20 μg of FMD virus per dose; or

g) 8-20 μg of FMD virus per dose; or

h) 8-12 μg of FMD virus per dose; or

i) 6-18 μg of FMD virus per dose.

18. A method of preventing FMD in an animal in need thereof, comprising administering to said animal the immunogenic composition according to claim 1 .

19. The method according to claim 18 , wherein the FMD virus composition is prepared by hollow fiber filtration.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2019
From: DOMINOWSKI, PAUL JOSEPH; HARDHAM, JOHN MORGAN; JACKSON, JAMES ALAN
To: ZOETIS LLC
Reel/Frame 050165/0329 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2019
From: RIEDER, AIDA; RODRIGUEZ, LUIS; KRUG, PETER; GAY, CYRIL
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF AGRICULTURE
Reel/Frame 050166/0343 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2019
From: ZOETIS LLC
To: ZOETIS SERVICES LLC
Reel/Frame 050166/0431 →
ASSIGNEE CHANGE OF ADDRESS Recorded Aug 26, 2019
From: ZOETIS SERVICES LLC
To: ZOETIS SERVICES LLC
Reel/Frame 050167/0871 →
Continuity (3)
Continuation 15543630
Provisional Application 62104314 · Jan 16, 2015
Related Publication 20200078456A1 · Mar 12, 2020
Cited By (1)
US 12,285,478