Li Jing, Yao Jun, Shan Huan, Chen Yongdi, Jiang Zheng-gang, Ren Jing-jing, Xu Kai-jin, Ruan Bing, Yang Shi-gui, Wang Bing, Xie Tian-sheng, Li Qian
a School of Medicine; Ningbo University ; Ningbo , China.
Hum Vaccin Immunother. 2015;11(5):1108-13. doi: 10.4161/21645515.2014.988547.
The aim of this study was to evaluate the one-month immune response to 2 different doses (10 and 20 μg) of recombinant hepatitis B vaccine in adults aged 20-46 y. Subjects who were negative for hepatitis B surface antigen (HBsAg), hepatitis B antibody (anti-HBs), and hepatitis B core antibody (anti-HBc) were recruited. The participants were divided into 2 groups: group I received 3 doses of 10 μg hepatitis B vaccine at 0, 1 and 3 months, and group II received 3 doses of 20 μg at the same time points. The anti-HBs levels were measured one month after the third vaccination. Among 739 subjects, 62 (9.70%) were positive for HBsAg, and 317 subjects were eligible. The anti-HBs seroprotection rates (anti-HBs ≥ 10 mIU/mL was considered to indicate seroprotection) after the third vaccination were 88.05% and 94.06% in group I and group II respectively, and the geometric mean titers were 91.69 and 290.23 mIU/mL respectively. The difference in the seroprotection rate was not significant (χ(2) = 2.566, P > 0.05), but the GMT after the third dose was significantly lower for group I than for group II (F = 20.587, P < 0.05). Better responses were observed in young adults, especially in group I. In group I, the seroprotection rate and GMT were significantly higher in the 20-35 y group than in the 36-46 y group (P < 0.05); there was no significant difference compared to group II (P > 0.05). The hepatitis B vaccine has good immunological effect; the 20 μg dose can be used in adults aged 20-46 y and the 10 μg dose can be used in subjects aged 20-35 years, and it should be tested on a larger number of subjects before recommending it for adult routine vaccination.
本研究旨在评估20至46岁成年人对两种不同剂量(10μg和20μg)重组乙型肝炎疫苗的1个月免疫反应。招募乙型肝炎表面抗原(HBsAg)、乙型肝炎抗体(抗-HBs)和乙型肝炎核心抗体(抗-HBc)均为阴性的受试者。参与者分为2组:I组在0、1和3个月时接种3剂10μg乙型肝炎疫苗,II组在相同时间点接种3剂20μg。在第三次接种后1个月测量抗-HBs水平。在739名受试者中,62名(9.70%)HBsAg呈阳性,317名受试者符合条件。I组和II组第三次接种后的抗-HBs血清保护率(抗-HBs≥10 mIU/mL被认为表示血清保护)分别为88.05%和94.06%,几何平均滴度分别为91.69和290.23 mIU/mL。血清保护率差异无统计学意义(χ(2)=2.566,P>0.05),但I组第三次接种后的GMT显著低于II组(F=20.587,P<0.05)。在年轻成年人中观察到更好的反应,尤其是在I组。在I组中,20至35岁组的血清保护率和GMT显著高于36至46岁组(P<0.05);与II组相比无显著差异(P>0.05)。乙型肝炎疫苗具有良好的免疫效果;20μg剂量可用于20至46岁的成年人,10μg剂量可用于20至35岁的受试者,在推荐用于成人常规疫苗接种之前,应在更多受试者身上进行测试。