首页> 美国卫生研究院文献>World Journal of Gastroenterology >Comparison of three different recombinant hepatitis B vaccines: GeneVac-B Engerix B and Shanvac B in high risk infants born to HBsAg positive mothers in India
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Comparison of three different recombinant hepatitis B vaccines: GeneVac-B Engerix B and Shanvac B in high risk infants born to HBsAg positive mothers in India

机译:印度HBsAg阳性母亲高危婴儿中三种不同的重组乙型肝炎疫苗:GeneVac-BEngerix B和Shanvac B的比较

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摘要

AIM: To evaluate a low cost Indian recombinant hepatitis B vaccine GeneVac-B® for its immunogenicity and safety in comparison to Engerix B® and Shanvac B® vaccine in high risk newborn infants born to hepatitis B surface antigen (HBsAg) positive mothers.METHODS: A total of 158 infants were enrolled in the study. Fifty eight infants were enrolled in the GeneVac-B® group while 50 each were included for Engerix B® and Shanvac B® groups. A three-dose regimen of vaccination; at birth (within 24 h of birth), 1st mo and 6 mo. were adopted with 10 μg dosage administered uniformly in all the three groups. Clinical and immunological parameters were assessed for safety and immunogenicity of the vaccines, in all the enrolled infants.RESULTS: Successful follow up until seven months of age was achieved in 83% (48/58) for GeneVac-B®, 76% (38/50) and 64% (32/50) for Engerix B® and Shanvac B® groups respectively. 100% seroconversion and seroprotection was achieved in all the three groups of infants. The geometric mean titers of anti-HBs one month after the completion of three dose of vaccination were 90.5, 80.9 and 72.5 mIU/mL in GeneVac-B®, Engerix B® and Shanvac B® vaccine group respectively. Furthermore the level of anti-HBs increases with age of babies who were born to HBsAg positive mothers. The GMT values of anti-HBs were 226.7, 193.9 and 173.6 mIU/mL respectively in GeneVac-B®, Engerix B® and Shanvac B® groups one year after the completion of the three doses of vaccine. No systemic reactions were reported in infants during the entire vaccination process of GeneVac-B® and the other two vaccines. Clinical safety parameters remained within the normal limits throughout the study period.CONCLUSION: The study concludes that there is no significant difference between the three recombinant hepatitis B vaccines. Administration of these vaccines within 24 h of birth to babies, born to HBsAg positive mothers will reduce the incidence of HBV infection.
机译:目的:与Engerix B ®和Shanvac B ®相比,评估低成本印度重组乙型肝炎疫苗GeneVac-B ®的免疫原性和安全性在乙型肝炎表面抗原(HBsAg)阳性母亲出生的高危新生儿中的疫苗。方法:共有158名婴儿参加了研究。 GeneVac-B ®组中有58名婴儿入组,而Engerix B ®和Shanvac B ®组中各有50名婴儿。三剂疫苗接种方案;在出生时(出生后24小时内),第一个月和第六个月。在所有三组中均以10μg剂量均匀给药。结果:对GeneVac-B ®的83%(48/58)的婴儿成功进行了随访,直到七个月大为止。 sup>,Engerix B ®和Shanvac B ®组分别为76%(38/50)和64%(32/50)。这三组婴儿均实现了100%的血清转化和血清保护。在完成三剂疫苗接种后一个月,抗-HBs的几何平均滴度在GeneVac-B ®,Engerix B ®中分别为90.5、80.9和72.5 mIU / mL。和Shanvac B ®疫苗组。此外,抗HBs水平随着HBsAg阳性母亲所生婴儿的年龄而增加。在GeneVac-B ®,Engerix B ®和Shanvac B ®中,抗HBs的GMT值分别为226.7、193.9和173.6 mIU / mL。 >组在完成三剂疫苗一年后。在GeneVac-B ®和其他两种疫苗的整个疫苗接种过程中,没有婴儿发生全身反应的报道。在整个研究期间,临床安全性参数均保持在正常范围内。结论:研究得出结论,三种重组乙型肝炎疫苗之间没有显着差异。在HBsAg阳性母亲出生的婴儿出生后24小时内施用这些疫苗将减少HBV感染的发生率。

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