Zhao Yu-Liang, Chen Yu-Guo, Li Jun, Han Ge-Xin, Tian Cha, Liang Jin-Long, Li Guo, Wang Zhi-Guo, Zhu Yong-Gui, Tian Zhi-Nian, Zhang Hua-Yuan, Wan Zong-Ju, Liang Zheng-Lun, Bi Sheng-Li
Hebei Provine Center for Disease Prevention and Control, Shijiazhuang 050021, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2004 Jun;25(6):470-3.
To study the safety and immunogenicity of the Bilive combined hepatitis A and B vaccine produced by Sinovac Biotech Co., Ltd.
Samples were selected from first year students of a senior high school (adults group) and first to fifth grade 1-5 students of 3 primary schools (children group). Those who were susceptible to both hepatitis A virus (HAV) and hepatitis B virus (HBV), HAV only or HBV only were assigned to group AB, A and B respectively and were vaccinated with three doses (0, 1 and 6 month schedule) of Bilive combined hepatitis A and B vaccine, inactivated hepatitis A vaccine and recombined hepatitis B vaccine respectively. The dosage for adult group was 500 U hepatitis A antigen and/or 10 micro g hepatitis B surface antigen and the dosage for children group was half the dosage of adult group. The potential adverse effects were observed within 72 hours after vaccination. Serum samples were collected for testing anti-HAV and anti-HBs at month 2 and 7 after the initial dose.
The rates of local adverse effects were 0.58% and 2.56% in children AB group and adults AB group and the general adverse effects rates were 9.88% and 5.45% respectively. Both local and general adverse effect rates were not significantly different to the control group. The sero-conversion rate of anti-HAV in children and adults AB group reached 100%, one month after 3 doses. The geometric mean titer (GMTs) reached 33,910 mIU/ml and 23,435 mIU/ml respectively, significant higher than that in control group (group A). The sero-conversion rates of anti-HBs were 97.30% and 96.63%, and GMTs were 103 mIU/ml and 102 mIU/ml in children and adults AB group respectively. No significant difference on sero-conversion and GMT was observed when compared with control group.
The Bilive combined hepatitis A and B vaccine had good safety profile, and the immunogenicity both on anti-HAV and anti-HBs was similar to that of separated components.
研究北京科兴生物制品有限公司生产的倍尔来福甲型乙型肝炎联合疫苗的安全性和免疫原性。
选取某高中一年级学生(成人组)及3所小学一至五年级学生(儿童组)为研究对象。将甲型肝炎病毒(HAV)和乙型肝炎病毒(HBV)均易感、仅对HAV易感或仅对HBV易感的人群分别纳入AB组、A组和B组,分别接种3剂(0、1和6月程序)倍尔来福甲型乙型肝炎联合疫苗、甲型肝炎灭活疫苗和重组乙型肝炎疫苗。成人组剂量为甲型肝炎抗原500 U和/或乙型肝炎表面抗原10 μg,儿童组剂量为成人组的一半。接种疫苗后72小时内观察潜在不良反应。在首剂接种后第2个月和第7个月采集血清样本检测抗-HAV和抗-HBs。
儿童AB组和成人AB组的局部不良反应发生率分别为0.58%和2.56%,全身不良反应发生率分别为9.88%和5.45%。局部和全身不良反应发生率与对照组相比均无显著差异。儿童和成人AB组3剂接种1个月后抗-HAV血清阳转率均达100%,几何平均滴度(GMT)分别达33910 mIU/ml和23435 mIU/ml,显著高于对照组(A组)。儿童和成人AB组抗-HBs血清阳转率分别为97.30%和96.63%,GMT分别为103 mIU/ml和102 mIU/ml。与对照组相比,血清阳转率和GMT无显著差异。
倍尔来福甲型乙型肝炎联合疫苗安全性良好,抗-HAV和抗-HBs免疫原性与各单苗相似。