1999•Chinese Journal of Clinical HepatologyRequires access

Study on a purified and inactivated japanese encephalitis vaccine prepared on Vero cells using SA 14142 attenuated virus strain

YU Yong-xi

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Abstract

Objective To develop a kind of new Japanese Encephalitis(JE) vaccine prepared on Vero cells. Methods A JE attenuated virus strain SA14142 was adapted on Vero cells for preparation of purified inactivated vaccine. Comparison of the growth curves of SA14142 in roller bottle and in spinner flask was made.After the virus inoculation and absorption on Vero cells for 2 hours, cultures were replaced with serumfree MEM, the culture supernatants were harvested on day 2,4,6 after inoculation. The virus fluids were pooled, concentrated by 8% PEG, and purified on 15%60% sucrose density gradients. The purified virus was inactivated with 0.02% formalin. Results It showed that virus titer was higher and maintained longer in roller bottle. Mice vaccinated twicely with 0.5 g dose of the purified inactivated vaccine induced neutralizing antibody titers equal to that of the mice vaccinated with primary hamster kidney inactivated vaccine. Conclusion This Vero cell prepared purified and inactivated JE vaccine made by SA14142 strain could be used for human as a kind of new JE vaccine.

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What this paper is about

Objective To develop a kind of new Japanese Encephalitis(JE) vaccine prepared on Vero cells. Methods A JE attenuated virus strain SA14142 was adapted on Vero cells for preparation of purified inactivated vaccine. Comparison of the growth curves of SA14142 in roller bottle and in spinner flask was made.After the virus inoculation and absorption on Vero cells for 2 hours, cultures were replaced with serumfree MEM, the culture supernatants were harvested on day 2,4,6 after inoculation. The virus fluids were pooled, concentrated by 8% PEG, and purified on 15%60% sucrose density gradients. The purified virus was inactivated with 0.02% formalin. Results It showed that virus titer was higher and maintained longer in roller bottle. Mice vaccinated twicely with 0.5 g dose of the purified inactivated vaccine induced neutralizing antibody titers equal to that of the mice vaccinated with primary hamster kidney inactivated vaccine. Conclusion This Vero cell prepared purified and inactivated JE vaccine made by SA14142 strain could be used for human as a kind of new JE vaccine.

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Available abstract

Objective To develop a kind of new Japanese Encephalitis(JE) vaccine prepared on Vero cells. Methods A JE attenuated virus strain SA14142 was adapted on Vero cells for preparation of purified inactivated vaccine. Comparison of the growth curves of SA14142 in roller bottle and in spinner flask was made.After the virus inoculation and absorption on Vero cells for 2 hours, cultures were replaced with serumfree MEM, the culture supernatants were harvested on day 2,4,6 after inoculation. The virus fluids were pooled, concentrated by 8% PEG, and purified on 15%60% sucrose density gradients. The purified virus was inactivated with 0.02% formalin. Results It showed that virus titer was higher and maintained longer in roller bottle. Mice vaccinated twicely with 0.5 g dose of the purified inactivated vaccine induced neutralizing antibody titers equal to that of the mice vaccinated with primary hamster kidney inactivated vaccine. Conclusion This Vero cell prepared purified and inactivated JE vaccine made by SA14142 strain could be used for human as a kind of new JE vaccine.

Key concepts: Vero cell, Japanese encephalitis vaccine, Virology, Titer, Inactivated vaccine, Virus, Japanese encephalitis, Inoculation

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