Immunogenicity and safety of an Escherichia coli-produced human papillomavirus (types 6/11/16/18/31/33/45/52/58) L1 virus-like-particle vaccine: a phase 2 double-blind, randomized, controlled trial

被引:5
作者
Hu, Yue-Mei [1 ]
Bi, Zhao-Feng [2 ,3 ]
Zheng, Ya [2 ,3 ]
Zhang, Li [4 ]
Zheng, Feng-Zhu [5 ]
Chu, Kai [1 ]
Li, Ya-Fei [2 ,3 ]
Chen, Qi [2 ,3 ]
Quan, Jia-Li [2 ,3 ]
Hu, Xiao-Wen [2 ,3 ]
Huang, Xing-Cheng [2 ,3 ]
Zhu, Kong-Xin [2 ,3 ]
Wang-Jiang, Ya-Hui [2 ,3 ]
Jiang, Han -Min [6 ]
Zang, Xia [6 ]
Liu, Dong-Lin [6 ]
Yang, Chang -Lin [6 ]
Pan, Hong-Xing [1 ]
Zhang, Qiu-Fen [5 ]
Su, Ying-Ying [2 ,3 ]
Huang, Shou-Jie [2 ,3 ]
Sun, Guang [5 ]
Huang, Wei-Jin [4 ]
Huang, Yue [2 ,3 ]
Wu, Ting [2 ,3 ]
Zhang, Jun [2 ,3 ]
Xia, Ning-Shao [2 ,3 ]
机构
[1] Publ Hlth Res Inst Jiangsu Prov, Jiangsu Prov Ctr Dis Control & Prevent, Nanjing 210009, Peoples R China
[2] Xiamen Univ, Sch Publ Hlth, State Key Lab Vaccines Infect Dis, Xiang Biomed Lab, Xiamen 361102, Peoples R China
[3] Xiamen Univ, State Key Lab Mol Vaccinol & Mol Diagnost, Natl Inst Diagnost & Vaccine Dev Infect Dis, Natl Innovat Platform Ind Educ Integrat Vaccine Re, Xiamen 361102, Peoples R China
[4] Natl Inst Food & Drug Control, Beijing 102629, Peoples R China
[5] Xiamen Innovax Biotech Co, Xiamen 361027, Peoples R China
[6] Dongtai Ctr Dis Control & Prevent, Yancheng 224200, Peoples R China
基金
中国国家自然科学基金;
关键词
Human papillomavirus; 9-valent human papillomavirus vaccine; Escherichia coli; Immunogenicity; Safety; FEMALES;
D O I
10.1016/j.scib.2023.09.020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Escherichia coli-produced human papillomavirus (HPV) 16/18 bivalent vaccine (Cecolin) has received prequalification by the World Health Organization based on its high efficacy and good safety profile. We aimed to evaluate the immunogenicity and safety of the second-generation nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine (Cecolin 9) through the randomized, blinded phase 2 clinical trial. Eligible healthy women aged 18-45 years were randomly (1:1) allocated to receive three doses of 1.0 mL (270 lg) of Cecolin 9 or placebo with a 0-1-6-month schedule. The primary endpoint was the sero-conversion rate and geometric mean titer of neutralizing antibodies (nAbs) one month after the full vac-cination course (month 7). The secondary endpoint was the safety profile including solicited adverse reactions occurring within 7 d, adverse events (AEs) occurring within 30 d after each dose, and serious adverse events (SAEs) occurring during the 7-month follow-up period. In total, 627 volunteers were enrolled and randomly assigned to Cecolin 9 (n = 313) or placebo (n = 314) group in Jiangsu Province, China. Almost all participants in the per-protocol set for immunogenicity (PPS-I) seroconverted for nAbs against all the nine HPV types at month 7, while two failed to seroconvert for HPV 11 and one did not seroconvert for HPV 52. The incidence rates of total AEs in the Cecolin 9 and placebo groups were 80.8% and 72.9%, respectively, with the majority of them being mild and recovering shortly. None of the SAEs were considered related to vaccination. In conclusion, the E. coli-produced 9-valent HPV (9vHPV) vaccine candidate was well tolerated and immunogenic, which warrants further efficacy studies in larger populations.(c) 2023 Science China Press. Published by Elsevier B.V. and Science China Press. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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收藏
页码:2448 / 2455
页数:8
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