Zhong Guo-Hua, Bi Zhao-Feng, Chu Kai, Zhang Li, Chen Lu, Zhu Kong-Xin, Quan Jia-Li, Nie Chu, Chen Qi, Qiu Ling-Xian, Xu Jin-Bo, Li Jia-Xue, Zhang Ming-Lei, Liu Sheng, Nie Ling-Ling, Li Kun, Su Ying-Ying, Huang Shou-Jie, Zhang Qiu-Fen, Huang Wei-Jin, Pan Hong-Xing, Wu Ting, Zhang Jun, Xia Ning-Shao
State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health, Xiamen University, Xiamen, China.
National Institute of Diagnostics and Vaccine Development in Infectious Diseases, National Innovation Platform for Industry-Education Integration in Vaccine Research, Xiamen University, Xiamen, China.
Lancet Reg Health West Pac. 2025 Aug 27;62:101671. doi: 10.1016/j.lanwpc.2025.101671. eCollection 2025 Sep.
Cecolin9, a second-generation 9-valent HPV vaccine derived from the WHO-prequalified Cecolin, has received marketing authorisation in China in May 2025. The non-inferiority of type-specific immune responses between Cecolin9 and Gardasil9 has been previously established at month 7 in Chinese women aged 18-26 years (NCT04782895). This study aimed to compare the plateau antibody levels between the two vaccines three years post the first dose.
This was a prospective extension study of a randomised, single-blind trial conducted in China (ClinicalTrials.gov, NCT06197802). All the participants included in the base study were invited to participate in this extension. Blood samples were collected at year 3 (median follow-up time of 34 months) for neutralising antibody detection, assessed by a triple-colour pseudovirion-based neutralisation assay. The primary outcome, geometric mean concentrations (GMCs), was analysed within three-dose recipients without major protocol violations, seronegative for the relevant type at baseline, and with available serum results at year 3. Non-inferiority of the GMC ratios (Cecolin9 Gardasil9) was determined as the lower bound of the two-sided 95% confidence interval (CI) in excess of 0.5.
Of the 487 participants enrolled in the base study, 82.8% (403/487) completed the three-year follow-up visit. The mean age at the first vaccination was 22.2 years among the 200 Cecolin9 recipients and 22.1 years among the 203 Gardasil9 recipients, respectively. The GMC ratios (Cecolin9 Gardasil9) for all nine HPV types ranged from 0.78 (95% CI 0.64-0.95) to 1.91 (95% CI 1.54-2.37), with the lower bounds of 95% CIs spanning from 0.64 to 1.54. Furthermore, sustained seropositivity rates were similar between groups, ranging from 84.7% to 100.0% in the Cecolin9 cohort and 86.2% to 100.0% in the Gardasil9 cohort. Notably, both groups presented consistent antibody decay trends over the observation period.
The Cecolin9 cohort demonstrated sustained non-inferior HPV type-specific plateau antibody levels compared to the Gardasil9 cohort, supporting Cecolin9's potential for enduring protection.
National Key Research and Development Plan, the National Natural Science Foundation of China, Beijing Natural Science Foundation, Fundamental Research Funds for the Central Universities, the Fieldwork Funds for graduate students of Xiamen University, and Xiamen Innovax.
希可洛9是一种源自世界卫生组织预认证的希可洛的第二代9价人乳头瘤病毒(HPV)疫苗,于2025年5月在中国获得上市许可。此前在中国18至26岁女性中进行的一项研究(NCT04782895)已证实,希可洛9与佳达修9在第7个月时各型特异性免疫反应的非劣效性。本研究旨在比较两疫苗首剂接种三年后的抗体平台期水平。
这是一项在中国进行的随机单盲试验的前瞻性扩展研究(ClinicalTrials.gov,NCT06197802)。基础研究中的所有参与者均受邀参加本扩展研究。在第3年(中位随访时间34个月)采集血样,采用基于三色假病毒的中和试验检测中和抗体。主要结局指标为几何平均浓度(GMC),在未违反主要方案、基线时相关型别血清学阴性且第3年有可用血清结果的三剂接种者中进行分析。GMC比值(希可洛9/佳达修9)的非劣效性定义为双侧95%置信区间(CI)下限超过0.5。
在基础研究纳入的487名参与者中,82.8%(403/487)完成了三年随访。200名希可洛9接种者首次接种时的平均年龄为22.2岁,203名佳达修9接种者为22.1岁。9种HPV型别的GMC比值(希可洛9/佳达修9)范围为0.78(95%CI 0.64 - 0.95)至1.91(95%CI 1.54 - 2.37),95%CI下限范围为0.64至1.54。此外,两组的持续血清阳性率相似,希可洛9队列中为84.7%至100.0%,佳达修9队列中为86.2%至100.0%。值得注意的是,在观察期内两组均呈现出一致的抗体衰减趋势。
与佳达修9队列相比,希可洛9队列显示出持续的HPV型特异性抗体平台期水平非劣效,支持希可洛9具有持久保护的潜力。
国家重点研发计划、中国国家自然科学基金、北京市自然科学基金、中央高校基本科研业务费、厦门大学研究生田野调查基金、厦门万泰沧海生物技术有限公司。