PCV/mycoplasma hyopneumoniae vaccine
This invention provides a combination vaccine which includes a porcine circovirus type 2 (PCV2) antigen and a cell free Mycoplasma hyopneumoniae (M. hyo) culture supernatant for protecting a pig against PCV2 and M. hyo infections, wherein the M. hyo culture supernatant is substantially free of PCV2 antibodies.
1. A combination vaccine comprising a porcine circovirus type 2 (PCV2) antigen and a cell free Mycoplasma hyopneumoniae (M. hyo) culture supernatant for protecting a pig against PCV2 and M. hyo infections, wherein the M. hyo culture supernatant is substantially free of PCV2 antibodies.
2. The combination vaccine of claim 1 , wherein the M. hyo culture supernatant has been treated with protein-A or protein-G.
3. The combination vaccine of claim 1 , wherein the vaccine is in the form of a ready-to-use liquid composition.
4. The combination vaccine of claim 1 , wherein the M. hyo culture supernatant comprises inactivated M. hyo antigen.
5. The combination vaccine of claim 1 , 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.
6. The combination vaccine of claim 1 , wherein the PCV2 antigen is in the form of a recombinant ORF2 protein.
7. The combination vaccine of claim 6 , wherein the recombinant ORF2 protein is expressed from a baculovirus vector.
8. The combination vaccine of claim 1 , wherein the vaccine further comprises at least one additional antigen that is protective against a microorganism that can cause disease in pigs.
9. The combination vaccine of claim 8 , wherein the microorganism comprises bacteria, viruses, or protozoans.
10. The combination vaccine of claim 9 , wherein the microorganism is selected from the group consisting of porcine reproductive and respiratory syndrome (PRRS) virus, Lawsonia intracellularis, Haemophilus parasuis, Pasteurella multocida, Streptococcum suis, Staphylococcus hyicus, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, Salmonella choleraesuis, Salmonella enteritidis, Erysipelothrix rhusiopathiae, Mycoplasma hyorhinis, Mycoplasma hyosynoviae , leptospira bacteria, 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) virus, a pathogen causative of Swine Transmissible Gastroenteritis, and combinations thereof.
11. The combination vaccine of claim 10 , wherein the vaccine comprises an inactivated Lawsonia intracellularis antigen or a PRRS virus antigen in the form of a genetically modified live PRRS virus.
12. The combination vaccine of claim 1 , wherein the vaccine further comprises an adjuvant.
13. The combination vaccine of claim 12 , 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.
14. The combination vaccine of claim 1 , wherein vaccine further comprises a pharmaceutically acceptable carrier.
15. The combination vaccine of claim 10 , wherein the vaccine further comprises an adjuvant.
16. The combination vaccine of claim 15 , 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.
17. The combination vaccine of claim 10 , wherein the vaccine further comprises a pharmaceutically acceptable carrier.
18. A method of eliciting a protective immune response in a pig against porcine circovirus type 2 (PCV2) and Mycoplasma hyopneumoniae (M. hyo) infections, the method comprising administering to the pig a combination vaccine comprising a PCV2 antigen and a cell free M. hyo culture supernatant, wherein the M. hyo culture supernatant is substantially free of PCV2 antibodies.
19. The method of claim 18 , wherein the combination vaccine is administered by a single dose or multiple doses.
20. The method of claim 19 , wherein the combination vaccine is administered by a single dose.
21. The method of claim 18 , wherein the combination vaccine is administered to pigs at 3 weeks of age or older.
22. The method of claim 18 , wherein the combination vaccine is administered intramuscularly, intradermally, transdermally, or subcutaneously.
23. The method of claim 18 , wherein the combination vaccine is administered to pigs having maternally derived antibodies against M. hyo and/or PCV2.
24. The method of claim 18 , wherein the combination vaccine is administered in conjunction with at least one additional antigen that is protective against a microorganism that can cause disease in pigs.