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孩尔来福甲型肝炎灭活疫苗0,12个月免疫程序研究
引用本文:任银海,陈江婷,吴文婷,公雪杰,张玉成,薛伟华,任一丰,韩连军,康文学,李胜平,刘崇柏.孩尔来福甲型肝炎灭活疫苗0,12个月免疫程序研究[J].中华流行病学杂志,2003,24(11):1013-1015.
作者姓名:任银海  陈江婷  吴文婷  公雪杰  张玉成  薛伟华  任一丰  韩连军  康文学  李胜平  刘崇柏
作者单位:1. 050400,河北省平山县卫生防疫站
2. 北京科兴生物制品有限公司
3. 中国疾病预防控制中心病毒病预防控制所
基金项目:国家“九五”医学科技攻关项目资助(96 90 6 0 3 0 4)
摘    要:目的 对孩尔来福 (HealiveR○)甲型肝炎 (甲肝 )灭活疫苗的安全性、免疫原性及适宜儿童的剂量进行研究。方法 在某山区两个农村筛选 4~ 10岁甲肝病毒抗体 (抗 HAV)阴性的 85名易感儿童。以自然村随机分为两组 ,按 0 ,12个月免疫程序分别接种北京科兴生物制品有限公司生产的每剂 2 50U 0 .5ml和 50 0U 1ml甲肝灭活疫苗 ,观察免疫后局部反应和全身反应 ,检测初次免疫 (初免 )后 2 1天、12个月及全程免疫后 1个月抗 HAV阳转率和抗体几何平均滴度 (GMT )。结果 两组均未见严重局部反应和全身反应 ;2 50U 0 .5ml组和 50 0U 1ml组初免后 2 1天 ,抗 HAV阳转率分别为94.4%和 10 0 .0 % ,GMT分别为 195mIU ml和 3 70mIU ml ;初免后 12个月抗 HAV全部阳转 ,GMT分别达 3 61mIU ml和 456mIU ml(P >0 .0 5) ;全程免疫后 1个月 ,GMT分别达 14 893mIU ml和2 1696mIU ml。结论 孩尔来福甲肝灭活疫苗的安全性和免疫原性好 ;每剂 2 50U 0 .5ml适宜儿童 ;0 ,12个月免疫程序更适宜中国儿童

关 键 词:孩尔来福甲型肝炎灭活疫苗  免疫程序  安全性  免疫原性  儿童
收稿时间:2003/3/6 0:00:00
修稿时间:2003年3月6日

The study on the 0,12 month vaccination schedule' of Healive inactivated hepatitis A vaccine in children
REN Yin-hai,CHEN Jiang-ting,WU Wen-ting,GONG Xue-jie,ZHANG Yu-cheng,XUE Wei-hu,REN Yi-feng,HAN Lian-jun,KANG Wen-xue,LI Sheng-ping and LIU Chong-bai.The study on the 0,12 month vaccination schedule'' of Healive inactivated hepatitis A vaccine in children[J].Chinese Journal of Epidemiology,2003,24(11):1013-1015.
Authors:REN Yin-hai  CHEN Jiang-ting  WU Wen-ting  GONG Xue-jie  ZHANG Yu-cheng  XUE Wei-hu  REN Yi-feng  HAN Lian-jun  KANG Wen-xue  LI Sheng-ping and LIU Chong-bai
Affiliation:Health and Anti-eqidemic Station of Pingshan County, Pingshan 050400, China.
Abstract:OBJECTIVE: To evaluate the safety, immunogenicity and fit dosage of Healive inactivated hepatitis A vaccine (HAV) in children. METHODS: A total of 85 susceptible aged 4 - 10 years with HAV seronegative children, had been enrolled from two adjacent villages in a county. The volunteers were randomized allocated into two groups and to receive a priming dose of 250 U/0.5 ml/dose or 500 U/1.0 ml/dose of Healive vaccine, produced by Sinovac Biotech Co, Ltd. A booster of the same dose was given at 12th month. Local and systemic side effects were examined and seroconversion rate as well as geometric mean titers of anti-HAV antibody were tested at 3-week, 12-month after the primary dose and at 1 month after the booster dose. RESULTS: The vaccine was well tolerated in both groups. At 21 days after the primary dose, the seroconversion rates were 94.4%, 100.0% and geometric mean titers (GMT) were 195 mIU/ml and 370 mIU/ml in 250 U and 500 U groups respectively. At 12 months after the primary dose, the seroconversion rate of anti-HAV was 100.0%, and GMT raised to 361 mIU/ml, 456 mIU/ml (P > 0.05) respectively. One month after the booster dose, GMT raised to 14 893 mIU/ml, 21 696 mIU/ml. CONCLUSION: GMT of the 0, 12 month schedule was higher than other schedule after the booster vaccination. The Healive inactivated vaccine can be used for emergency vaccination. The Healive inactivated vaccine produced by Sinovac Company Ltd was safe and highly immunogenic. Two hundred and fifty U/dose was considered appropriate for children.
Keywords:Inactivated hepatitis A vaccine  Immunogeni city  Safety  Immunization-schedule
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