IP Library Granted Patent US 8,637,046
Granted Patent B2
US 8,637,046 · App. 13/121,566 · Granted Jan 28, 2014

Bovine herpes virus-1 compositions, vaccines and methods

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Quick Facts
Patent No.
US 8,637,046
App. No.
13/121,566
Granted
Jan 28, 2014
Kind
B2
Abstract

The disclosure relates generally to the treatment or prevention of disease in cattle. More particularly, the invention is directed to the production and use of modified bovine herpesvirus 1 (BHV-1) and their use in compositions and vaccines that protect cattle from BHV-1 infection while not suppressing the immunological response in the host. In one example, the invention is directed to the use of modified BHV-1, administered with additional immunogens, either through co-administration and/or through administration in combination vaccines, and the use of these vaccines for the protection of cattle from disease. In one example, use of the modified BHV-1 in the administered compositions facilitates an immune response to or against the additional immunogens.

Claims (19)

1. A composition, comprising:

a) a live BHV-1 that has modifications of UL49.5 and at least one additional gene encoding protein that can affect a host immunological response to an immunogen; and

b) an additional immunogen which is not encoded by a foreign gene inserted in the genome of the live BHV-1,

where following administration of the composition to a host, a ratio of IgG1/IgG2 for IgG specific for the additional immunogen in the host is higher than a ratio of IgG1/IgG2 for IgG specific for the additional immunogen in a host administered a composition of live BHV-1 that does not have the modifications and the additional immunogen.

2. The composition of claim 1 , where the at least one additional gene is UL41 or Us4.

3. The composition of claim 1 , where following administration of the composition of live BHV-1 that has the modifications and the additional immunogen to the host, cell samples obtained from blood of the host and contacted with the additional immunogen have higher levels of interleukin-2 (IL-2) as compared to levels of IL-2 from cell samples obtained from blood of the host administered the composition of live BHV-1 that does not have the modifications and the additional immunogen, and contacted with the additional immunogen.

4. The composition of claim 3 , where the at least one additional gene is UL41.

5. The composition of claim 1 , where the additional immunogen includes a bacterial, viral or parasitic immunogen.

6. The composition of claim 1 , where the additional immunogen includes an immunogen from Bovine Viral Diarrhea Virus (BVDV) I, BVDV II, BVDV III, Bovine Respiratory Syncytial Virus (BRSV), Parainfluenza 3 Virus (PI3), Rotavirus (BRV), Coronavirus (BCV), Mannheimia haemolytica, Histophilus somni, Mycoplasma bovis, Leptospira species, Vibrio species, Clostridia species, Pasteurella multocida, Fusobacterium necrophorum, E. coli O157:H7, Salmonella enterica, Neospora caninum or Trichomonas species.

7. The composition of claim 1 , where the additional immunogen includes LkT from Mannheimia haemolytica.

8. A method for eliciting an immunological response in a host, comprising administering to the host a composition including:

a) an immunogen other than a BHV-1 antigen (non-BHV-1 immunogen), which is not encoded by a foreign gene inserted in a BHV-1 genome; and

b) a live BHV-1 that has modifications of UL49.5 and at least one additional gene encoding protein that can affect a host immunological response to an immunogen,

where following administration of the composition to the host, a ratio of IgG1 to IgG2 in the host for IgG specific for the non-BHV-1 immunogen is higher than a ratio of IgG1 to IgG2 for IgG specific for the non-BHV-1 immunogen in a host administered a composition of the non-BHV-1 immunogen and live BHV-1 that does not have the modifications.

9. The method of claim 8 , where the non-BHV-1 immunogen and the live BHV-1 are co-administered or administered to the host in a combination vaccine.

10. The method of claim 8 , where the at least one additional gene is UL41 or Us4.

11. The method of claim 8 , where following administration of the composition of non-BHV-1 immunogen and live BHV-1 that has the modifications to the host, cell samples obtained from blood of the host and contacted with the non-BHV-1 immunogen have higher levels of interleukin-2 (IL-2) as compared to levels of IL-2 from cell samples obtained from blood of the host administered the composition of the non-BHV-1 immunogen and live BHV-1 that does not have the modifications, and contacted with the non-BHV-1 immunogen.

12. The method of claim 11 , where the at least one additional gene is UL41.

13. The method of claim 8 , wherein the host is an ungulate.

Assignments (4)
CHANGE OF NAME Recorded Apr 23, 2018
From: NOVARTIS TIERGESUNDHEIT AG
To: ELANCO TIERGESUNDHEIT AG
Reel/Frame 046246/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2015
From: NOVARTIS AG
To: NOVARTIS TIERGESUNDHEIT AG
Reel/Frame 034926/0844 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2011
From: OSTERRIEDER, NIKOLAUS; KAUFER, BENEDIKT B.
To: CORNELL UNIVERSITY
Reel/Frame 026192/0711 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2011
From: RAJU SEETHARAMAN, GOPINATH; HARLAND, RICHARD; ALBEE, LEE DAVID, II; PATEL, MAYUR NAVNITBHAI
To: NOVARTIS AG
Reel/Frame 026192/0736 →