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大肠杆菌重组颗粒性戊型肝炎疫苗对恒河猴的免疫保护

Protective Efficacy of a Particulate Recombinant(E.coli)Hepatitis E Vaccine on Rhesus Monkey

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【作者】 张军李益民李少伟欧山海黄果勇何志强葛胜祥鲜阳凌逄淑强夏宁邵

【Author】 ZHANG Jun 1,LI Yi ming 2,LI Shao wei 1,OU Shan hai 1, HUANG Guo yong 3,HE Zhi qiang 1, GE Sheng xiang 1,XIAN Yang lin 2,PANG Su qiang 2,XIA Ning shao 1* (1.The Key Laboratory of Ministry of Education for Cell Biology and Tumor Cell Engineering,Xiamen University,Xiamen 361005,China; 2.Beijing Wantai Biological Pharmacy Enterprise Co.,Beijing 102200,China; 3.Center of Disease Control and Prevention of Guanxi,Nanning 430021,China)

【机构】 厦门大学细胞生物学与肿瘤细胞工程教育部重点实验室北京万泰生物药业有限公司广西壮族自治区疾病控制中心厦门大学细胞生物学与肿瘤细胞工程教育部重点实验室 厦门361005北京102200厦门361005广西南宁430021厦门361005

【摘要】 大肠杆菌表达的戊型肝炎病毒 (HEV)衣壳蛋白ORF2片段HEV 2 39重组蛋白颗粒 ,经铝佐剂吸附后 ,分别以5 μg、1 0 μg和 2 0 μg剂量免疫恒河猴 ,2 8天时以相同剂量加强免疫 1次 ,3周后分别以不同病毒滴度的基因Ⅰ型或基因Ⅳ型HEV静脉攻击。结果 ,加强后 3周 ,3个免疫剂量组猴的抗体几何平均滴度分别为 1∶2 71 75、1∶344 0 9、1∶4 16 0 7,以世界卫生组织参比血清定量 ,则分别为 1 0 98IU/ml,1 35 7IU/ml、1 72 4IU/ml。每个剂量免疫组及对照组各有 3只猴接受 1 0 7病毒滴度基因Ⅰ型HEV感染 ,对照组 3只猴均被成功感染 ,2只出现肝炎 ;2 0 μg免疫组 3只猴均未被感染 ;1 0 μg和 5 μg免疫组各有 2只猴未被感染 ,另 1只猴出现短暂感染 ,免疫猴均未出现肝炎。 3个剂量免疫组及对照组另外 3只猴 ,接受 1 0 4病毒滴度基因Ⅰ型HEV感染 ,对照组 3只猴均被感染 ,1只出现肝炎 ;而免疫猴均未被感染 ,也未出现肝炎。 3只 1 0 μg免疫猴和 3只对照猴分别接受 1 0 7病毒滴度基因Ⅳ型HEV感染 ,对照组均被感染并出现肝炎 ,而免疫组均未出现肝炎 ,有 2只未被感染 ,另 1只被短暂感染。另有 3只 1 0 μg免疫猴和 3只对照猴分别接受 1 0 4病毒滴度基因Ⅳ型HEV感染 ,对照组均被感染 ,而免疫组均未被感染。这些结果表明 :HEV

【Abstract】 An E.coli expressed recombinant protein HEV 239,which was derived from capsid protein ORF2 of hepatitis E virus(HEV)and aggregated into virus like particle,was adsorbed with alum adjuvant,then immunized rhesus monkeys with 5μg,10μg,or 20μg dosages.Three weeks after the animals were boosted on day 28,different virus dosages of a HEV genotype Ⅰ strain and a HEV genotype Ⅳ strain were used to challenge the monkeys as well as the control monkeys intravenously. The results showed that the geometry mean titer of anti HEV of three vaccine dosage groups were 1∶27*!175,1∶34*!409 and 1∶41*!607 respectively.The anti HEV quantity calculated by ELISA using a WHO reference serum were 1*!098 IU/ml,1*!357 IU/ml and 1*!724 IU/ml respectively.Three monkeys of each vaccinated groups and control group were challenged with 10 7 virus titer of HEV genotype Ⅰ strain.While all three monkeys of control group were infected by the virus and two suffered from hepatitis,all three monkeys of 20μg vaccinated group,two of 10μg vaccinated group and two of 5μg vaccinated group were protected from infection,and moreover all vaccinated monkeys were protected against hepatitis.Another three monkeys of each vaccinated group and control group were challenged with 10 4 virus titer of HEV genotype Ⅰ strain. While all three monkeys of the control group were infected and one suffered from hepatitis,all the vaccinated monkeys were protected from infection as well as hepatitis.Three monkeys vaccinated with 10μg vaccine and three control monkeys when challenged with 10 7 virus titer of HEV genotype Ⅳ strain,all three monkeys of the control group were infected and suffered from hepatitis,and the vaccinated monkeys all were protected from hepatitis and two were protected from virus infection.Three monkeys of 10μg vaccinated group and control group when challenged with 10 4 virus titer of HEV genotype Ⅳ strain, the monkeys of the control group were all infected,the vaccinated monkeys were protected from infection.These results indicated that the HEV 239 vaccine could protect rhesus monkey completely against hepatitis E,and partially protect against HEV infectivity. Besides,the protective efficacy of this vaccine against heterologous HEV challenge was similar as against homologous challenge.

【基金】 福建省科技重大项目 ( 2 0 0 2F0 13 ) ;教育部跨世纪人才优秀培养计划
  • 【文献出处】 病毒学报 ,Chinese Journal of Virology , 编辑部邮箱 ,2004年01期
  • 【分类号】R392.1
  • 【被引频次】15
  • 【下载频次】282
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