Method for producing rabies vaccine for human

A rabies vaccine and human production technology, applied in the field of human rabies vaccine production, can solve the problems of low; Chinese patent disclosure, low vaccine quality, low production capacity, etc.

Active Publication Date: 2013-10-16
CHENGDU KANGHUA BIOLOGICAL PROD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Chinese Patent Publication No. is the patent application of CN1274607A, discloses a kind of method that uses spinning bottle technology to produce rabies vaccine, and virus strain is CTN strain, and this patent is owing to what adopting is spinning bottle technology, thereby production capacity is lower; Chinese Patent Publication No. is The patent application of CN1712068A discloses a method for producing rabies vaccine using diploid cells. The production process is a rotary bottle, and the virus strains are aG strain and CTN strain. Because the patent uses a rotary bottle process, the production capacity is low; The patent application with the publication number CN101028514A discloses a method for producing rabies vaccine by cultivating Vero cells in a bioreactor. The virus strain is a PV strain. Since the cell matrix used in this patent is Vero cells, there is a biological safety problem of DNA residues. Also did not use the linear amplification technology of bioreactor; Chinese Patent Publication No. is the patent application of CN101716341A, discloses the method that utilizes diploid cell to produce rabies vaccine, and cell matrix is ​​MRC-5, IMR-90, WI 38, 2BS, KMB17, the virus strain is PM strain
However, with the development of rabies vaccine production technology up to now, there are still problems of low production capacity and low vaccine quality

Method used

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Examples

Experimental program
Comparison scheme
Effect test

no. 1 approach

[0014] (1) Resuscitated human diploid cells (WI-38) and inoculated them into square flasks;

[0015] (2) After the cells are full of the square bottle, amplify the passage according to the ratio of 1:3;

[0016] (3) When the cells grow to a certain amount, they are inoculated into a 7.5L bioreactor; the working volume of the bioreactor is 5L, equipped with 2-20g / L microcarriers;

[0017] (4) When the microcarriers in the 7.5L bioreactor are covered with cells, the cell density reaches 10 6 When it is above / ml, inoculate the cells into a 50L bioreactor; the working volume of the bioreactor is 35L, equipped with 2-20g / L microcarriers;

[0018] (5) When the microcarriers in the 50L bioreactor are covered with cells, the cell density reaches 10 6 When it is above / ml, inoculate into a 500L bioreactor; the working volume of the bioreactor is 350L, equipped with 2-20g / L microcarriers;

[0019] (6) When the microcarriers in the 500L bioreactor are covered with cells, the cell den...

no. 2 approach

[0024] (1) Resuscitate human diploid cells (2BS) and inoculate them into square flasks;

[0025] (2) After the cells are full of the square bottle, amplify the passage according to the ratio of 1:3;

[0026] (3) When the cell density reaches 10 6 / ml or more, inoculate the cells into a 14L bioreactor; the working volume of the bioreactor is 10L, equipped with 2-20g / L microcarriers;

[0027] (4) Wait until the microcarriers in the 14L bioreactor are covered with cells, that is, the cell density reaches 10 6 When it is above / ml, inoculate the cells into a 100L bioreactor; the working volume of the bioreactor is 70L, equipped with 2-20g / L microcarriers;

[0028] (5) When the microcarriers in the 100L bioreactor are covered with cells, the cell density reaches 10 6 When it is above / ml, inoculate the cells into a 1000L bioreactor; the working volume of the bioreactor is 700L, equipped with 2-20g / L microcarriers;

[0029] (6) When the microcarriers in the 1000L bioreactor are ...

no. 3 approach

[0034] (1) Resuscitate human diploid cells (2BS) and inoculate them into square flasks;

[0035] (2) After the cells are full of the square bottle, amplify the passage according to the ratio of 1:3;

[0036] (3) When the cells grow to a certain amount, inoculate the cells into a 14L bioreactor; the working volume of the bioreactor is 10L, equipped with 2-20g / L microcarriers;

[0037] (4) When the microcarriers in the 14L bioreactor are full of cells, the cell density reaches 10 6 When it is above / ml, inoculate the cells into a 100L bioreactor; the working volume of the bioreactor is 70L, equipped with 2-20g / L microcarriers;

[0038] (5) When the microcarriers in the 100L bioreactor are covered with cells, the cell density reaches 10 6 When it is above / ml, inoculate the cells into a 1000L bioreactor; the working volume of the bioreactor is 700L, equipped with 2-20g / L microcarriers;

[0039] (6) When the microcarriers in the 1000L bioreactor are covered with cells, the cell...

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PUM

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Abstract

The invention relates to a method for producing a rabies vaccine for human, comprising the following steps of: culturing human diploid cell lines by adopting a linear amplification technique of three or more levels of bioreactors; after the human diploid cell line in each level of bioreactor reaches 106 / ml, carrying out the vaccination on the next level of bioreactor; after the human diploid cell line in the last level of bioreactor grows on a microcarrier until the density reaches 106 / ml, vaccinating rabies virus strains; propagating viruses on cells by vaccinating the rabies virus strains, harvesting virus stock solutions, and inactivating, concentrating and purifying the harvested virus stock solutions to obtain the rabies vaccine for human. By using the linear amplification technique of the bioreactor to culture the human diploid cell lines, the cells do not contain exogenous pollution factors and tumorigenicity, and the residual DNA of the cells has no danger, and the rabies vaccine for human has the advantages of good immunizing effect and high safety and meets the requirement of large-scale industrial production of the rabies vaccine.

Description

technical field [0001] The invention relates to a production method of a vaccine, in particular to a production method of a human rabies vaccine. Background technique [0002] Rabies is a zoonotic viral infectious disease caused by rabies virus. Once a person is bitten by a sick animal and becomes ill, the virus rate is extremely high. Timely vaccination and preventive vaccination are clinically effective means of preventing and treating rabies. [0003] There are mainly four types of rabies vaccines currently on the market: the first is chicken embryo and duck embryo vaccines, which have low yields, high production intensity, and the possibility of exogenous virulence factors; the second is hamster vaccines. Kidney cell primary culture vaccines also have the problems of low vaccine yield, high production intensity, and the possibility of exogenous virulence factors; the third is the vaccine produced by Vero subcultured cells. This variety can solve the production capacity...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K39/205A61P31/14
Inventor 蔡勇杨刚强
Owner CHENGDU KANGHUA BIOLOGICAL PROD
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