IP Library › Granted Patent US 11,141,472
Granted Patent B2
US 11,141,472 · App. 16/859,093 · Granted Oct 12, 2021

Mycoplasma hyopneumoniae vaccine

Inventors: Jeffrey E. Galvin (Lincoln, NE); Gregory P. Nitzel (Paw Paw, MI); John Keith Garrett (North Wilkesboro, NC); James R. Kulawik, II (Lincoln, NE); Tracy L. Ricker (Portage, MI); Megan Marie Smutzer (Kalamazoo, MI)
Assignee: Zoetis Services LLC
A61K39/0241A61K39/0208A61K39/12A61K39/295A61K39/39C07K14/30C12N1/36A61K2039/521A61K2039/5252A61K2039/552A61K2039/55566A61K2039/70C12N2750/10021C12N2750/10034C12N2750/10063C12N2770/10034
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Quick Facts
Patent No.
US 11,141,472
App. No.
16/859,093
Granted
Oct 12, 2021
Kind
B2
Abstract

This invention provides a Mycoplasma hyopneumoniae (M. hyo) antigen that is compatible with antigens from other swine pathogens, wherein the M. hyo antigen is a cell free M. hyo culture supernatant which is substantially free of swine IgG.

Claims (30)

1. A Mycoplasma hyopneumoniae (M. hyo) antigen that is compatible with antigens from other swine pathogens, wherein the M. hyo antigen is a cell free M. hyo culture supernatant which is substantially free of swine IgG.

2. The antigen of claim 1 , wherein the M. hyo antigen is inactivated.

3. The antigen of claim 1 , wherein the M. hyo culture supernatant has been separated from insoluble cellular material by centrifugation, filtration, or precipitation.

4. The antigen of claim 1 , wherein the M. hyo culture supernatant has been protein A-treated or protein G-treated.

5. An immunogenic composition comprising the antigen of claim 1 .

6. The composition of claim 5 , wherein the composition further comprises at least one additional antigen that is protective against a swine pathogen selected from the group consisting of porcine circovirus type 2 (PCV2), porcine reproductive and respiratory syndrome virus (PRRSV), porcine parvovirus (PPV), Haemophilus parasuis, Pasteurella multocida, Streptococcum suis, Staphylococcus hyicus, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, Salmonella choleraesuis, Salmonella enteritidis, Erysipelothrix rhusiopathiae, Mycoplasma hyorhinis, Mycoplasma hyosynoviae , leptospira bacteria, Lawsonia intracellularis , swine influenza virus (SIV), Escherichia coli antigen, Brachyspira hyodysenteriae , porcine respiratory coronavirus, Porcine Epidemic Diarrhea (PED) virus, rotavirus, Porcine enteroviruses, Encephalomyocarditis virus, a pathogen causative of Aujesky's Disease, Classical Swine fever (CSF) and a pathogen causative of Swine Transmissible Gastroenteritis, or combinations thereof.

7. The composition of claim 6 , wherein the at least one additional antigen is a porcine circovirus type 2 (PCV2) antigen, a PRRS virus antigen, a Lawsonia intracellularis antigen or a combination thereof.

8. The composition of claim 7 , wherein the composition elicits a protective immune response against M. hyo and PCV2.

9. The composition of claim 7 , wherein the composition elicits a protective immune response in a pig against M. hyo, PCV2 and PRRS virus.

10. The composition of claim 7 , wherein the composition elicits a protective immune response in a pig against M. hyo, PCV2 and Lawsonia intracellularis.

11. The composition of claim 7 , wherein the PCV2 antigen is in the form of a chimeric type-1-type 2 circovirus, said chimeric virus comprising an inactivated recombinant porcine circovirus type 1 expressing the porcine circovirus type 2 ORF2 protein.

12. The composition of claim 7 , wherein the PCV2 antigen is in the form of a recombinant ORF2 protein.

13. The composition of claim 12 , wherein the recombinant ORF2 protein is expressed from a baculovirus vector.

14. The composition of claim 5 , wherein the composition further comprises an adjuvant.

15. The composition of claim 14 , wherein the adjuvant is selected from the group consisting of an oil-in-water adjuvant, a polymer and water adjuvant, a water-in-oil adjuvant, an aluminum hydroxide adjuvant, a vitamin E adjuvant and combinations thereof.

16. The composition of claim 5 , wherein the composition further comprises a pharmaceutically acceptable carrier.

17. The composition of claim 5 , wherein the composition elicits a protective immune response against M. hyo when administered as a single dose administration.

18. The composition of claim 6 , wherein the composition elicits a protective immune response against M. hyo and the at least one additional swine pathogen when administered as a single dose or two doses.

19. A method of immunizing a pig against Mycoplasma hyopneumoniae (M. hyo) which comprises administering to the pig the composition of claim 5 .

20. The method of claim 19 , wherein the composition is administered intramuscularly, intradermally, transdermally, or subcutaneously.

21. The method of claim 19 , wherein the composition is administered in a single dose.

22. The method of claim 19 , wherein the composition is administered in conjunction with at least one additional antigen that is protective against a swine pathogen selected from the group consisting of porcine circovirus type 2 (PCV2), porcine reproductive and respiratory syndrome virus (PRRSV), porcine parvovirus (PPV), Haemophilus parasuis, Pasteurella multocida, Streptococcum suis, Staphylococcus hyicus, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, Salmonella choleraesuis, Salmonella enteritidis, Erysipelothrix rhusiopathiae, Mycoplasma hyorhinis, Mycoplasma hyosynoviae , leptospira bacteria, Lawsonia intracellularis , swine influenza virus (SIV), Escherichia coli antigen, Brachyspira hyodysenteriae , porcine respiratory coronavirus, Porcine Epidemic Diarrhea (PED) virus, rotavirus, Porcine enteroviruses, Encephalomyocarditis virus, a pathogen causative of Aujesky's Disease, Classical Swine fever (CSF) and a pathogen causative of Swine Transmissible Gastroenteritis, or combinations thereof.

23. The method of claim 19 , wherein the composition is administered to pigs having maternally derived antibodies against M. hyo.

24. The method of claim 22 , wherein the composition is administered to pigs having maternally derived antibodies against M. hyo and the at least one other swine pathogen.

25. The method of claim 19 , wherein the composition is administered to pigs at 3 weeks of age or older.

26. The method of claim 22 , wherein the composition is administered as a single dose or two doses.

27. A kit comprising a Mycoplasma hyopneumoniae (M. hyo) antigen that is compatible with antigens from other swine pathogens, wherein the M. hyo antigen is a cell free M. hyo culture supernatant which is substantially free of swine IgG.

28. The kit of claim 27 , wherein the M. hyo culture supernatant has been separated from insoluble cellular material by centrifugation, filtration, or precipitation.

29. The kit of claim 27 , further comprising comprises at least one additional antigen that is protective against a swine pathogen selected from the group consisting of porcine circovirus type 2 (PCV2), porcine reproductive and respiratory syndrome virus (PRRSV), porcine parvovirus (PPV), Haemophilus parasuis, Pasteurella multocida, Streptococcum suis, Staphylococcus hyicus, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, Salmonella choleraesuis, Salmonella enteritidis, Erysipelothrix rhusiopathiae, Mycoplasma hyorhinis, Mycoplasma hyosynoviae , leptospira bacteria, Lawsonia intracellularis , swine influenza virus (SIV), Escherichia coli antigen, Brachyspira hyodysenteriae , porcine respiratory coronavirus, Porcine Epidemic Diarrhea (PED) virus, rotavirus, Porcine enteroviruses, Encephalomyocarditis virus, a pathogen causative of Aujesky's Disease, Classical Swine fever (CSF) and a pathogen causative of Swine Transmissible Gastroenteritis, or combinations thereof.

30. The kit of claim 29 , wherein the at least one additional antigen is a porcine circovirus type 2 (PCV2) antigen, a PRRS virus antigen, a Lawsonia intracellularis antigen or a combination thereof.