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中国研发的针对H5高致病性禽流感的疫苗。

Vaccines developed for H5 highly pathogenic avian influenza in China.

作者信息

Qiao Chuanling, Tian Guobin, Jiang Yongping, Li Yanbing, Shi Jianzhong, Yu Kangzhen, Chen Hualan

机构信息

Animal Influenza Laboratory of the Ministry of Agriculture, Harbin 150001, People's Republic of China.

出版信息

Ann N Y Acad Sci. 2006 Oct;1081:182-92. doi: 10.1196/annals.1373.022.

Abstract

Since the first detection of highly pathogenic H5N1 avian influenza virus from sick goose in Guangdong province in China in 1996, scientists in China started to develop vaccines for avian influenza pandemic preparedness. An H5N2 inactivated vaccine was produced from a low pathogenic virus, A/turkey/England/N-28/73, and was used for the buffer zone vaccination in the H5N1 outbreaks in 2004 in China. We also generated a low pathogenic H5N1 reassortant virus A/Harbin/Re-1/2003 (Re-1) that derives its HA and NA genes from GSGD/96 virus and six internal genes from the high-growth A/Puerto Rico/8/34 (PR8) virus by using plasmid-based reverse genetics. The inactivated vaccine derived from Re-1 strain could induce more than 10 months protective immune response in chickens after one dose inoculation, and most importantly, this vaccine is immunogenic for geese and ducks. An H5N1 fowlpox vectored live vaccine was also generated by inserting the HA and NA genes of GSGD/96 virus in the genome of a fowlpox vaccine strain. Laboratory tests indicated that after one dose of immunization of this vaccine, chickens could develop an over than 40 weeks protective immune response against H5N1 virus challenge.

摘要

自1996年在中国广东省从病鹅中首次检测到高致病性H5N1禽流感病毒以来,中国科学家就开始研发用于防范禽流感大流行的疫苗。一种H5N2灭活疫苗是由低致病性病毒A/火鸡/英格兰/N - 28/73生产的,并在中国2004年H5N1疫情期间用于缓冲区疫苗接种。我们还通过基于质粒的反向遗传学方法,构建了一种低致病性H5N1重配病毒A/哈尔滨/Re - 1/2003(Re - 1),其HA和NA基因来源于GSGD/96病毒,六个内部基因来源于高生长性的A/波多黎各/8/34(PR8)病毒。由Re - 1株衍生的灭活疫苗在鸡接种一剂后可诱导超过10个月的保护性免疫反应,最重要的是,该疫苗对鹅和鸭具有免疫原性。通过将GSGD/96病毒的HA和NA基因插入禽痘疫苗株的基因组中,还构建了一种H5N1禽痘载体活疫苗。实验室测试表明,鸡接种一剂该疫苗后,可对H5N1病毒攻击产生超过40周的保护性免疫反应。

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