Jiangsu Province Center for Disease Control and Prevention, Jiangsu, China.
Taizhou City Center for Disease Control and Prevention, Taizhou, China.
Asia Pac J Clin Oncol. 2020 Dec;16(6):392-399. doi: 10.1111/ajco.13398. Epub 2020 Aug 11.
In 9-17-year-old Chinese girls, the AS04-adjuvanted HPV-16/18 vaccine (AS04-HPV-16/18) given as three-dose schedule induced high antibody levels, which were noninferior 1 month after the third dose to those observed in 18-25-year-old Chinese women in a large efficacy study. We assessed the persistence of antibodies 8-9 years after vaccination in the same subjects.
This follow-up phase III, open-label study (NCT03355820) included subjects who had received three doses of AS04-HPV-16/18 in the initial trial (NCT00996125). Serum antibody concentrations were assessed by ELISA and compared to antibody persistence observed in 18-25-year-old Chinese women 6 years after first vaccination in the efficacy study (NCT00779766).
Out of the 227 enrolled subjects, 223 were included in the per-protocol immunogenicity analysis. Mean interval from first AS04-HPV-16/18 dose to blood sampling was 101.4 months (8.5 years). For antibodies against HPV-16 and -18, 8.5 years after first vaccine dose all subjects remained seropositive and antibody. Geometric mean concentrations (GMCs) were 1236.3 (95% confidence interval [CI]: 1121.8; 1362.4) and 535.6 (95% CI: 478.6; 599.4) ELISA Units/mL, respectively. These seropositivity rates and antibody GMCs were higher than those observed 6 years after first vaccination of 18-25-year-old women.
Sustained anti-HPV-16 and -18 immune responses were observed 8-9 years after AS04-HPV-16/18 vaccination of 9-17 year-old Chinese girls that were higher than the ones observed 6 years after first vaccination in Chinese adult women in whom AS04-HPV-16/18 efficacy against cervical intraepithelial neoplasia of grade ≥2 was demonstrated.
在 9-17 岁中国女孩中,三剂次 AS04 佐剂 HPV-16/18 疫苗(AS04-HPV-16/18)接种后诱导产生了高抗体水平,这些抗体水平在接种后 1 个月与大型疗效研究中 18-25 岁中国女性观察到的水平相当。我们评估了同一受试者接种 8-9 年后抗体的持久性。
这是一项随访 III 期、开放性标签研究(NCT03355820),纳入了初始试验(NCT00996125)中接受三剂 AS04-HPV-16/18 接种的受试者。通过 ELISA 评估血清抗体浓度,并与疗效研究中接种 6 年后 18-25 岁中国女性观察到的抗体持久性进行比较(NCT00779766)。
在 227 名入组受试者中,223 名符合方案免疫原性分析。首次接种 AS04-HPV-16/18 疫苗至采血的平均时间间隔为 101.4 个月(8.5 年)。对于 HPV-16 和 -18 的抗体,在首次疫苗接种后 8.5 年,所有受试者均保持血清阳性和抗体。几何平均浓度(GMC)分别为 1236.3(95%置信区间 [CI]:1121.8;1362.4)和 535.6(95% CI:478.6;599.4)ELISA 单位/mL。这些血清阳性率和抗体 GMC 均高于 18-25 岁女性接种 6 年后的水平。
在 9-17 岁中国女孩中接种 AS04-HPV-16/18 疫苗 8-9 年后,持续观察到抗 HPV-16 和 -18 的免疫应答,其水平高于在 HPV-16/18 疗效证明对宫颈上皮内瘤变≥2 级的中国成年女性中首次接种 6 年后观察到的水平。