医学
养生
免疫原性
接种疫苗
乙肝疫苗
随机对照试验
内科学
血清转化
人口
免疫学
外科
乙型肝炎病毒
免疫系统
抗体
病毒
乙型肝炎表面抗原
环境卫生
作者
Yongliang Feng,Yao Tian,Yizhuo Gao,Hong Li,Shuang Dong,Yuan-Ting Wu,Yuan Liu,Jing Li,Chunhua Liu,Jinxia Liu,Tongchuan Xue,Yuan Yuan,Junhua Wu,Fuzhen Wang,Xiaofeng Liang,Suping Wang
标识
DOI:10.1080/14760584.2021.1977629
摘要
Background We evaluated the safety and immunogenicity of four doses of 20 or 60 µg, and the immunogenicity and compliance of the short-term vaccination regimen (0, 1, and 2 months) among patients receiving MMT.Research design and methods We conducted a randomized controlled trial among 303 patients receiving MMT who were randomized to receive 3 or 4 doses of 20 or 60 µg of recombinant hepatitis B vaccine.Results At month 7, the seroconversion rates in both IM20 × 4 and IM60 × 4 groups were numerically higher than the IM20 × 3 group (P > 0.05). The high-level responses and geometric mean concentration (GMC) of anti-HBs in both IM20 × 4 and IM60 × 4 groups were significantly higher than the IM20 × 3 group (P < 0.05). The completion rate of the short-term high-strength vaccination group was significantly higher than the standard vaccination group (P < 0.05), with similar immunogenicity (P > 0.05).Conclusions Both the high-strength and standard-strength four-dose hepatitis B vaccine regimens could improve the immune response for patients receiving MMT. The high-strength short-term vaccination regimen could improve compliance and attain comparable immunogenicity with the standard vaccination regimen. The high-strength short-term vaccination regimen is recommended and the fourth dose is encouraged for this population considering the compliance and immunogenicity.Clinical trial registration ClinicalTrials.gov (NCT03962816)
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