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作 者:迎新玲 邢玉兰 沈莉 周少莲 陈红[1] 王申[1] 刘立荣 康沛[1] 谢祖婉 杨素芝[1] 黄悦 倪承瑞 王文[1] 任贵方[1]
机构地区:[1]北京市卫生防疫站,中国预防医学科学院病毒学研究所,北京市佑安医院,北京铁路局铁路中心卫生防疫站
出 处:《中华实验和临床病毒学杂志》1994年第2期101-104,共4页Chinese Journal of Experimental and Clinical Virology
摘 要:将76例HBsAg和HBeAg双阳性母亲所生新生儿随机分为A、B两组,分别接种3针20μg基因疫苗和1针HBIG加3针10μg基因疫苗。将239名乙肝易感学龄儿童(7~9岁)随机分为3组,Ⅰ组接种3针10μg基因疫苗,Ⅱ组接种3针5μg基因疫苗,Ⅲ组接种3针10μg血源疫苗。接种程序和接种部位均按"北京市乙肝疫苗免疫接种规程"进行,并于初次免疫后7个月、12个月和24个月采血检测HBsAg、抗-HBs和抗-HBc。结果表明,①新生儿免疫保护率:T24时A、B两组分别为80.92%和96.97%;用Fisher精确x2检验P<0.05,两组间差异有显著性;②新生儿免疫后抗体应答:T24时A、B两组的抗-HBs阳转率分别为70.27%和94.74%,GMT(mIU/ml,下同)分别为494和388,经统计学分析,两组间抗体阳转率差异有显著性,表明,HBIG加3针10μg基因疫苗联合使用效果优于单用3针20μg疫苗组;③学龄儿童3组的抗-HBs阳转率:在T7、T12时均在96%以上,各组间未见显著性差异。在T24时,3组的抗-HBs阳转率分别为98.65%、97.40%和98.63%,GMT为1062、533和7?Seventy-six newborn babies who had been borne from HBsAg (+) and HBeAg (+) mothers were randomly divided into Group A and Group B, and were inoculated with 3 injections of 20μg genetic engineering vaccine and with 3 injection of hightiter immunoglobulin against HBV plus 3 injections of 10μg genetic engineering vaccine, respectively. Two-hundred and thirty-nine school-aged children(aged 7-9 years) who were susceptible to type B hepatitis were randomly divided into 3 groups.Group Ⅰ received 3 injections of 10μg genetic engineering vaccine. Group Ⅱ received 3 injections of 5μg genetic engineering vaccine. Group Ⅲ received 3 injections of 10μg blood-derived vaccine. The procedure and site of injection were taken according to the 'Beijing Immunization Regulations for Type B Hepatitis'. Blood was collected at 7 months, 12 months and 24 months after the first injection and assayed for HBsAg, anti-HBs and anti-HBc. Results showed that: (1) The immune protection rates of newborn babies: They were 80.92% and 96.97% for Group Ⅰ and Group Ⅱ, respectively at 24 months. The difference was significant as examined by the Fisher accurate X2 test (P < 0.05). (2) The antibody response after immunizstion of newborn babies: The anti-HBs positive conversion rates of Group Ⅰ and Group Ⅱ at 24 months were 70.27% and 94.74%, respectively. and theGMT (mIU / ml) were 494 and 388, respectively. Statistical analysis disclosed that the difference in antibody positive conversion rates was significant, showing that the efficacy of Group Ⅱ was superior to that of Group Ⅰ. (3) The anti-HBs conversion rates of 3 groups of school-aged children: They were all over 96% at 7 months and 12 months. There was no significant difference among them. At 24 months, the anti-HBs conversion rates of 3 groups were 98.65%, 97.40% and 98.63%, respectively, and the GMT of Group Ⅰ was higher than that of Group Ⅲ, and those of both Group Ⅰ and Group Ⅲ were higher than that of Group Ⅱ.
分 类 号:R512.620.3[医药卫生—内科学]
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