Method for preparing hogcholera vaccine

A swine fever vaccine and cell technology, which is applied in the field of swine fever vaccine preparation, can solve the problems such as the inability to greatly improve the vaccine yield, contamination of foreign viruses, low toxin-producing titers, etc., and achieve good safety and immune effect, High efficiency of virus infection and the effect of improving immunity

Inactive Publication Date: 2010-08-11
PU LIKE BIO ENG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] Among them, the tissue seedling method and the primary bovine testicular cell seedling method generally have shortcomings such as low yield, low efficiency, foreign virus contamination, low toxin production titer, and large batch-to-batch differences; the cell line method, although it has solved the problem of exogenous virus Pollution problem, the titer of toxin production has also been greatly improved, and the difference between batches has also been reduced, but the vaccine production still cannot be greatly improved, and the process is cumbersome and inefficient, resulting in a lot of waste of personnel

Method used

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  • Method for preparing hogcholera vaccine
  • Method for preparing hogcholera vaccine
  • Method for preparing hogcholera vaccine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] 1 Viruses and cell lines

[0036] The virus used to make the swine fever live virus vaccine is an attenuated strain of classical swine fever (strain C), which has no pathogenicity after a pathogenicity test. The porcine testis cell line (ST), which has good sensitivity to the virus strain, is used as the cell line for making seedlings, so as to infect and multiply the classical swine fever virus in large quantities.

[0037] 2 Preparation method

[0038] (1) Inoculate the porcine testis cell line (ST), which is a cell line for making seedlings, into liquid medium (comprising 10% sheep serum, 0.01mol / L NaHCO) added with MEM liquid medium 3 , 0.1mg / ml kanamycin sulfate (kanamycinsulfate), 100,000IU penicillin G sodium salt (Penicillin G Sodium), pH value is 7.2) and in the carrier tank of BioNoc II polyester fiber; the amount of microcarrier is per 500ml culture fluid Add 5.5 g of microcarriers, and the initial inoculum size of cells is 3.0 × 108 cells / g microcarriers. ...

Embodiment 2

[0058] The comparative test of the swine fever live virus vaccine that embodiment 2 the present invention makes and similar products

[0059] 1. Materials

[0060] (1) Vaccine: 3 batches of swine fever live virus vaccine that embodiment 1 makes, batch number: CSF-T01, CSF-T02, CSF-T03. 1 batch of swine fever live virus vaccine (produced by roller bottle culture system), batch number: CSF-RB01.

[0061] (2) Experimental pigs: select feeding farms or designated pig farms that meet the national experimental animal standards to supply, 8-week-old weaned susceptible piglets, body weight 18-25kg, all negative for classical swine fever antibodies (serum neutralizing antibodies); note Observation before seedlings was carried out for 7 days, once a day in the morning and afternoon, and those with normal body temperature, spirit and appetite were selected for use.

[0062] (3) Attacking virus: CSFV (CSFV) Shimen is a strong strain.

[0063] 2. Method

[0064] (1) Property inspection...

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Abstract

The invention discloses a method by adopting cell micro-carrier suspension culture system to prepare hogcholera (CSF) vaccine, which comprises the following steps that: (1) cells for preparing the vaccine is inoculated into a carrier tank containing culture liquid and micro-carriers, and the cells are uniformly mixed with the micro-carriers, so the cells are attached onto the micro-carriers; (2) when the quantity of the cells is increased to 5 to 40 times of the initial inoculation concentration, the hog cholera virus (HCLV) is inoculated onto the cells so as to breed the virus according to the virus multiple of infection (M.O.I) is of the ratio of 0.01 to 1; and (3) the prepared virus liquid is mixed, appropriate freezing drying protective agent is added, the virus liquid is quantitatively packed after being uniformly mixed with the freezing drying protective agent to be frozen and dried so as to obtain the hogcholera vaccine (CSF). The method which is adopted to produce the hogcholera vccine has the advantages that the concentration of the cultured cells is high, the cells can be continuously cultured, the virus yield is high, the immunity effect of the vaccine is high, the safety is good, and the like, and has complete immunity protection effect against the attack of the hog cholera virus.

Description

technical field [0001] The invention belongs to the technical field of veterinary biological products, and in particular relates to a method for preparing a swine fever vaccine. Background technique [0002] Classical Swine fever (CSF for short), also known as Hog cholera or European swine fever, is a viral infectious disease with acute or hyperacute fever in pigs, clinically characterized by Rapid dissemination, fever, and typical hemorrhagic lesions can be seen on autopsy. Swine fever can infect pigs of all ages and is prevalent throughout the year with high morbidity and mortality, which is extremely harmful to pigs. This disease is one of the most important infectious diseases threatening the pig industry. The World Organization for Animal Health (OIE) lists swine fever as one of the 16 notifiable infectious diseases of category A, and China defines it as a severe infectious disease. [0003] Compulsory immunization with swine fever live virus vaccine is currently the...

Claims

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Application Information

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IPC IPC(8): A61K39/187A61K47/26A61K47/46C12N7/00C12R1/93A61P31/14
Inventor 张许科孙进忠乔荣岑陶家权王延辉张海洋习向锋李三
Owner PU LIKE BIO ENG
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