IP Library Granted Patent US 9,878,030
Granted Patent B2
US 9,878,030 · App. 13/825,050 · Granted Jan 30, 2018

BVDV vaccine

Inventors: Martin Beer (Greifswald-Insel Riems, DE); Ilona Reimann (Greifswald-Insel Riems, DE); Patricia Koenig (Greifswald-Insel Riems, DE)
Assignee: Intervet Inc.
A61K39/12A61K39/295A61K39/40A61K39/42C07K14/005A61K2039/5254A61K2039/552A61K2039/70C12N2770/24322C12N2770/24334C12N2770/24362
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Quick Facts
Patent No.
US 9,878,030
App. No.
13/825,050
Granted
Jan 30, 2018
Kind
B2
Abstract

The present invention relates to BVD virus and to its uses, to vaccines and combination vaccines comprising such a virus, their use as a medicament, their use in the treatment of Bovine Viral Diarrhea and to methods for the preparation of such vaccines.

Claims (22)

1. A combination vaccine for the protection against Bovine Viral Diarrhea Virus (BVDV) that comprises a first live attenuated BVDV, a second live attenuated BVDV, and a pharmaceutically acceptable carrier;

wherein the first BVDV and the second BVDV are either both Type 1 BVDVs or both Type 2 BVDVs;

wherein the first BVDV and the second BVDV each comprise a BVDV E2 gene; and

wherein when the first BVDV and the second BVDV are both Type 1 BVDVs, the E2 gene of the second BVDV is replaced by a BVDV E2 gene of a Type 2 BVDV; and wherein when the first BVDV and the second BVDV are both Type 2 BVDVs, the E2 gene of the second BVDV is replaced by a BVDV E2 gene of a Type 1 BVDV.

2. A combination vaccine for the protection against Bovine Viral Diarrhea Virus (BVDV) that comprises a first live attenuated BVDV, a second live attenuated BVDV, and a pharmaceutically acceptable carrier;

wherein the first BVDV and the second BVDV are either both Type 1 BVDVs or both Type 2 BVDVs;

wherein the first BVDV and the second BVDV each comprise a BVDV E1 gene and a BVDV E2 gene; and

wherein when the first BVDV and the second BVDV are both Type 1 BVDVs, both the BVDV E2 gene and the BVDV E1 gene of the second BVDV are replaced by a BVDV E2 gene and a BVDV E1 gene of a Type 2 BVDV; and wherein when the first BVDV and the second BVDV are both Type 2 BVDVs, both the E2 and the E1 gene of the second BVDV is replaced by a BVDV E2 and BVDV E1 gene of a Type 1 BVDV.

3. The combination vaccine according to claim 1 , wherein the backbone of the first and second BVDV belongs to a Type 1 BVDV and the BVDV E2 gene of the second BVDV belongs to a Type 2 BVDV.

4. The combination vaccine according to claim 1 , wherein the backbone of the first and second BVDV belongs to a Type 2 BVDV and the BVDV E2 gene of the second BVDV belongs to a Type 1 BVDV.

5. The combination vaccine according to claim 1 , characterised in that said first BVDV and said second BVDV have the same backbone.

6. The combination vaccine according to claim 5 , characterised in that said backbone is BNDV a Type 1 BVDV.

7. The combination vaccine according to claim 1 , wherein said first BVDV or said second BVDV comprises a deletion in a gene selected from the group consisting of the N pro gene and the E rns gene.

8. The combination vaccine according to claim 1 , characterized in that said vaccine or combination vaccine comprises an additional antigen of a virus or micro-organism pathogenic to ruminants, an antibody against said antigen or genetic information encoding an immunogenic polypeptide of said virus or micro-organism.

9. The combination vaccine according to claim 8 , characterized in that said virus or micro-organism pathogenic to ruminants is selected from the group of Bovine Rotavirus, Bovine Herpesvirus, Parainfluenza Type 3 virus, Bovine Paramyxovirus, Bluetongue virus, Foot and Mouth Disease virus, Pasteurella haemolytica and Bovine Respiratory Syncytial Virus.

10. The combination vaccine according to claim 1 , characterised in that it is in a freeze-dried form.

11. A method for making a combination vaccine according to claim 1 , comprising the step of mixing a live attenuated Type 1 BVDV that comprises a Type 1 BVDV E2 gene, a live attenuated Type 1 BVDV that comprises a Type 2 BVDV E2 gene in place of a Type 1 BVDV E2 gene, and a pharmaceutically acceptable carrier.

12. The combination vaccine according to claim 2 , wherein the backbone of the first and second BVD virus belongs to a Type 1 BVDV and the BVDV E2 gene of the second BVD virus belongs to a Type 2 BVDV.

13. The combination vaccine according to claim 12 , wherein said first BVDV and said second BVDV have the same backbone.

14. The combination vaccine according to claim 13 , wherein said first BVDV or said second BVDV comprises a deletion in a gene selected from the group consisting of the N pro gene and the E rns gene.

15. The combination vaccine according to claim 2 , characterised in wherein the backbone of the first and second BVD virus belongs to a Type 2 BVDV and the BVDV E2 gene and E1 gene of the second BVD virus belongs to a Type 1 BVDV.

16. A method for making a combination vaccine according to claim 1 , comprising the step of mixing a live attenuated Type 2 BVDV that comprises a Type 2 BVDV E2 gene, a live attenuated Type 2 BVDV that comprises a Type 1 BVDV E2 gene in place of a Type 2 BVDV E2 gene, and a pharmaceutically acceptable carrier.

Assignments (3)
CHANGE OF ADDRESS Recorded Sep 26, 2023
From: INTERVET INC.
To: INTERVET INC.
Reel/Frame 065028/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2014
From: INTERVET INTERNATIONAL B.V.
To: INTERVET INC.
Reel/Frame 032047/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2014
From: BEER, MARTIN; REIMANN, ILONA; KOENIG, PATRICIA
To: INTERVET INTERNATIONAL B.V.
Reel/Frame 032036/0545 →
Priority Claims (1)
EP 10177931 · Sep 21, 2010 · regional
Continuity (2)
Provisional Application 61385010 · Sep 21, 2010
Related Publication 20130195892A1 · Aug 1, 2013