Lactobacillus paracasei strain
US-12152232-B2 · Nov 26, 2024 · US
US9273281B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9273281-B2 |
| Application number | US-201314135796-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2013 |
| Priority date | Dec 28, 2012 |
| Publication date | Mar 1, 2016 |
| Grant date | Mar 1, 2016 |
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The present invention relates to a method for the preparation of an immunogenic composition for the treatment and/or prophylaxis of mycoplasma infections in a subject comprising the cultivation of mycoplasma bacteria in a serum-reduced or swine serum-free, eukaryotic cell system; obtaining an antigen of the mycoplasma bacteria; and addition of a pharmaceutically acceptable carrier. Further, the present invention relates to the immunogenic composition obtainable by said method and a method for immunizing a subject comprising the administration of said immunogenic composition to a subject.
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The invention claimed is: 1. A method for the preparation of an immunogenic composition for the treatment of mycoplasma infections in a subject comprising a bacterin comprising one or more antigens selected from M. hyorhinis, M. hyosynoviae , and M. hyopneumoniae , and any combination thereof, wherein at least one of bacteria M. hyorhinis, M. hyosynoviae , and/or M. hyopneumoniae is co-cultivated in a eukaryotic cell system comprising McCoy cells comprising the steps of: a. cultivating mycoplasma in a serum-reduced, McCoy cell system; b. obtaining such a mycoplasma bacteria as a bacterin comprising mycoplasma antigens; and c. adding a pharmaceutically acceptable carrier. 2. The method of claim 1 , wherein the serum is free of swine serum. 3. The method of claim 1 , wherein the mycoplasma bacteria are cultivated in the absence of serum. 4. The method of claim 1 , wherein the antigen has an increased immunogenicity compared to an antigen obtained from mycoplasma bacteria cultivated in a cell free culturing system. 5. The method of claim 1 , wherein the bacterins are formalin or binary ethylenimine (BEI) inactivated bacterins. 6. The method of claim 1 , wherein the immunogenic composition comprises a bacterin comprising a combination of antigens of M. hyorhinis and M. hyopneumoniae. 7. The method of claim 1 , wherein the immunogenic composition comprises a bacterin comprising a combination of antigens of M. hyopneumoniae, M. hyorhinis and M. hyosynoviae. 8. The method of 1, wherein said immunogenic composition is formulated for a single-dose administration. 9. The method of claim 1 , wherein said subject is a swine. 10. The method of claim 1 , wherein said pharmaceutically acceptable carrier is selected from the group consisting of solvents, dispersion media, coatings, stabilizing agents, diluents, preservatives, antibacterial and antifungal agents, isotonic agents, adsorption delaying agents, adjuvants, immune stimulants, and combinations thereof. 11. The method of claim 1 , wherein said pharmaceutically acceptable carrier is an adjuvant selected from the group consisting of aluminum hydroxide, aluminum phosphate, saponins, water-in-oil emulsion, oil-in-water emulsion, water-in-oil-in-water emulsion, polymers of acrylic or methacrylic acid, copolymers of maleic anhydride and alkenyl derivative, the RIBI adjuvant system, Block co-polymer, SAF-M, monophosphoryl lipid A, Avridine lipid-amine, heat-labile enterotoxin from E. coli (recombinant or otherwise), cholera toxin, IMS 1314, muramyl dipeptide, and combinations thereof. 12. The method of claim 1 , wherein said pharmaceutically acceptable carrier is a water-in-oil-in-water emulsion or a carbomer.
Antibacterial agents · CPC title
Immunostimulants · CPC title
Bacteria; Culture media therefor · CPC title
Adaptation or attenuation of cells · CPC title
Kidney cells · CPC title
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