Combined live vaccine against porcine reproductive and respiratory syndrome and pseudorabies, and preparation method thereof
A technology for respiratory syndrome and porcine pseudorabies, applied in antiviral agents, pharmaceutical formulations, viral antigen components, etc., can solve problems such as difficult to achieve effects
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[0080] Compared with the prior art, the preparation method provided by the invention has many advantages. For example, its preparation process is simple and stable, easy to operate, high virus content, small batch-to-batch differences, easy to control quality, can significantly improve vaccine yield and quality, and reduce allergic reactions. The porcine reproductive and respiratory syndrome and pseudorabies combined live vaccine obtained by using the preparation method of the present invention has good safety and high immune efficacy, and has a good immune protection effect against the virulent attack of porcine reproductive and respiratory syndrome and pseudorabies.
[0081] The invention also provides a PRRSV and PRV dual vaccine composition prepared by the method of the invention.
[0082] The invention also provides the use of the vaccine composition in preparing biological products for preventing or treating porcine reproductive and respiratory syndrome and porcine pseudorabi...
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[0091] Example 1 Preparation of highly pathogenic porcine reproductive and respiratory syndrome and pseudorabies combined live vaccine
[0092] The highly pathogenic porcine reproductive and respiratory syndrome and pseudorabies combined live vaccine is prepared by the following method:
[0093] (1) Select susceptible cells as cells for seedling production: select African green monkey kidney cells (Marc-145) as PRRSV susceptible cells, and select Marc-145, bovine kidney cells (MDBK) and bovine testis passage cells (BT) Passage cells are susceptible to PRV.
[0094] (2) Passage and culture of cells for seedling production: the above-mentioned passaged cells are digested and passaged with EDTA-trypsin cell dispersion, and then cultured with cell growth fluid to form a monolayer of passaged cells, used for continued passage or virus inoculation; cell culture The temperature is 36-37°C.
[0095] (3) Propagation of virus seeds for production:
[0096] A. Propagation of virus seeds for the ...
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[0106] Example 2 Purity test of highly pathogenic PRRSV and PRV dual live vaccine
[0107] According to the description on pages 15, 19, and 20 of Appendix of the "Chinese Ming Republic Veterinary Pharmacopoeia" (2005 edition), the dual live vaccine prepared in Example 1 was tested, and the results showed that the dual live vaccine was free of bacteria, molds and mycoplasma Growth, no foreign virus contamination.
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