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大肠杆菌生产的 HPV 双价疫苗在女童中接种 2 剂和 3 剂与在年轻女性中接种 3 剂的免疫原性非劣效性研究。

Immunogenicity noninferiority study of 2 doses and 3 doses of an Escherichia coli-produced HPV bivalent vaccine in girls vs. 3 doses in young women.

机构信息

Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, 210009, China.

The State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, Collaborative Innovation Center of Biologic Products, School of Public Health, Xiamen University, Xiamen, 361102, China.

出版信息

Sci China Life Sci. 2020 Apr;63(4):582-591. doi: 10.1007/s11427-019-9547-7. Epub 2019 Jun 21.

Abstract

A new HPV-16/18 bivalent vaccine expressed by the Escherichia coli has been proven to be efficacious in adult women. A randomized, immunogenicity noninferiority study of this candidate vaccine was conducted in December 2015 in China. Girls aged 9-14 years were randomized to receive 2 doses at months 0 and 6 (n=301) or 3 doses at months 0, 1 and 6 (n=304). Girls aged 15-17 years (n=149) and women aged 18-26 years (n=225) received 3 doses. The objectives included noninferiority analysis of the IgG geometric mean concentration (GMC) ratio (95% CI, lower bound>0.5) to HPV-16 and HPV-18 at month 7 in girls compared with women. In the per-protocol set, the GMC ratio of IgG was noninferior for girls aged 9-17 years receiving 3 doses compared with women (1.76 (95% CI, 1.56, 1.99) for HPV-16 and 1.93 (95% CI, 1.69, 2.21) for HPV-18) and noninferior for girls aged 9-14 years receiving 2 doses compared with women (1.45 (95% CI, 1.25, 1.62) for HPV-16 and 1.17 (95% CI, 1.02, 1.33) for HPV-18). Noninferiority was also demonstrated for neutralizing antibodies. The immunogenicity of the HPV vaccine in girls receiving 3 or 2 doses was noninferior compared with that in young adult women.

摘要

一种新的 HPV-16/18 二价疫苗已被证明在成年女性中有效。该候选疫苗的一项在 2015 年 12 月在中国进行的随机、免疫原性非劣效性研究。9-14 岁的女孩被随机分为两组,分别在 0 月和 6 月接受 2 剂(n=301)或 0 月、1 月和 6 月接受 3 剂(n=304)。15-17 岁的女孩(n=149)和 18-26 岁的女性(n=225)接种 3 剂。研究目的包括在接种后 7 个月时比较女孩组与女性组 HPV-16 和 HPV-18 的 IgG 几何平均浓度(GMC)比值(95%CI,下限>0.5)的非劣效性分析。在符合方案集分析中,3 剂接种的 9-17 岁女孩组与女性组相比,HPV-16 和 HPV-18 的 IgG GMC 比值均具有非劣效性(HPV-16 为 1.76(95%CI,1.56,1.99),HPV-18 为 1.93(95%CI,1.69,2.21)),2 剂接种的 9-14 岁女孩组与女性组相比也具有非劣效性(HPV-16 为 1.45(95%CI,1.25,1.62),HPV-18 为 1.17(95%CI,1.02,1.33))。中和抗体也显示出非劣效性。与年轻成年女性相比,接种 3 剂或 2 剂 HPV 疫苗的女孩的免疫原性非劣效。

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