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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

机译:对女孩进行2剂和3剂大肠埃希菌生产的HPV二价疫苗的免疫原性非劣效性研究对年轻女性进行3剂免疫原性研究

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摘要

A new HPV-16/18 bivalent vaccine expressed by the 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 ( =301) or 3 doses at months 0, 1 and 6 ( =304). Girls aged 15–17 years ( =149) and women aged 18–26 years ( =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.
机译:业已证明,新的HPV-16 / 18二价疫苗可在成年女性中有效。该候选疫苗的随机免疫原性非劣性研究于2015年12月在中国进行。 9-14岁的女孩被随机分配在0和6个月接受2剂(= 301)或在0、1和6个月接受3剂(= 304)。 15-17岁的女孩(= 149)和18-26岁的妇女(= 225)接受了3剂。目的包括对女性第7个月与HPV-16和HPV-18的IgG几何平均浓度(GMC)比率(95%CI,下限> 0.5)进行非劣效性分析。在每项协议中,接受3剂的9-17岁女孩的IgG的GMC比值不逊于女性(HPV-16为1.76(95%CI,1.56,1.99),女性为1.93(95%CI,1.69)) ,接受HPV-18的女性为2.21),接受9到14岁女孩接受2剂的非劣于女性(HPV-16为1.45(95%CI,1.25,1.62),女性为1.17(95%CI,1.02,1.33) HPV-18)。还证明中和抗体具有非劣效性。与年轻成年女性相比,接受3或2剂疫苗的女孩中HPV疫苗的免疫原性不逊色。

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