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Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial

BACKGROUND: A safe and highly efficacious Escherichia coli (E. coli)-produced HPV 16/18 bivalent vaccine has been prequalified by the World Health Organization. Here, we conducted a single-center, open-label, dose-escalation phase 1 clinical trial to evaluate the safety and immunogenicity of the sec...

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Autores principales: Chu, Kai, Bi, Zhao-Feng, Huang, Wei-Jin, Li, Ya-Fei, Zhang, Li, Yang, Chang-Lin, Jiang, Han-Min, Zang, Xia, Chen, Qi, Liu, Dong-Lin, Pan, Hong-Xing, Huang, Yue, Zheng, Feng-Zhu, Zhang, Qiu-Fen, Sun, Guang, Su, Ying-Ying, Huang, Shou-Jie, Pan, Hui-Rong, Wu, Ting, Hu, Yue-Mei, Zhang, Jun, Zhu, Feng-Cai, Xia, Ning-Shao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240382/
https://www.ncbi.nlm.nih.gov/pubmed/37283969
http://dx.doi.org/10.1016/j.lanwpc.2023.100731
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author Chu, Kai
Bi, Zhao-Feng
Huang, Wei-Jin
Li, Ya-Fei
Zhang, Li
Yang, Chang-Lin
Jiang, Han-Min
Zang, Xia
Chen, Qi
Liu, Dong-Lin
Pan, Hong-Xing
Huang, Yue
Zheng, Feng-Zhu
Zhang, Qiu-Fen
Sun, Guang
Su, Ying-Ying
Huang, Shou-Jie
Pan, Hui-Rong
Wu, Ting
Hu, Yue-Mei
Zhang, Jun
Zhu, Feng-Cai
Xia, Ning-Shao
author_facet Chu, Kai
Bi, Zhao-Feng
Huang, Wei-Jin
Li, Ya-Fei
Zhang, Li
Yang, Chang-Lin
Jiang, Han-Min
Zang, Xia
Chen, Qi
Liu, Dong-Lin
Pan, Hong-Xing
Huang, Yue
Zheng, Feng-Zhu
Zhang, Qiu-Fen
Sun, Guang
Su, Ying-Ying
Huang, Shou-Jie
Pan, Hui-Rong
Wu, Ting
Hu, Yue-Mei
Zhang, Jun
Zhu, Feng-Cai
Xia, Ning-Shao
author_sort Chu, Kai
collection PubMed
description BACKGROUND: A safe and highly efficacious Escherichia coli (E. coli)-produced HPV 16/18 bivalent vaccine has been prequalified by the World Health Organization. Here, we conducted a single-center, open-label, dose-escalation phase 1 clinical trial to evaluate the safety and immunogenicity of the second-generation nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. METHOD: Twenty-four eligible volunteers aged 18–45 years were enrolled in January 2019 in Dongtai, China and received 0.5 mL (135 μg) or 1.0 mL (270 μg) of the candidate vaccine with a 0/1/6-month dose-escalation schedule. Local and systemic adverse events (AEs) occurring within 30 days after each vaccination and serious adverse events (SAEs) occurring within 7 months were recorded. Blood samples from each participant were collected before and 2 days after the first and third vaccinations to determine changes in laboratory parameters. Serum IgG and neutralizing antibody (nAb) levels against each HPV type at month 7 were analyzed (ClinicalTrials.gov: NCT03813940). FINDINGS: The incidences of total AEs in the 135 μg and 270 μg groups were 66.7% and 83.3%, respectively. All AEs were mild or moderate, and no SAEs were reported. No clinically significant changes were found in paired blood indices before or after any of the vaccinations. All the participants in the per-protocol set except for two who failed to seroconvert for HPV 11 or 58 in the 135 μg group seroconverted at month 7 for both IgG and nAbs. INTERPRETATION: The candidate E. coli-produced 9vHPV vaccine has been preliminarily proven to be well tolerated and immunogenic, which encourages further studies in large cohorts with a wider age range. FUNDING: This study was supported by the 10.13039/501100001809National Natural Science Foundation of China, 10.13039/501100003392Fujian Provincial Natural Science Foundation, Fujian Province Health and Education Joint Research Program, Xiamen Science and Technology Plan Project, 10.13039/501100012226Fundamental Research Funds for the Central Universities, 10.13039/501100005150CAMS Innovation Fund for Medical Sciences of China, and Xiamen Innovax Biotechnology Co., Ltd.
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spelling pubmed-102403822023-06-06 Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial Chu, Kai Bi, Zhao-Feng Huang, Wei-Jin Li, Ya-Fei Zhang, Li Yang, Chang-Lin Jiang, Han-Min Zang, Xia Chen, Qi Liu, Dong-Lin Pan, Hong-Xing Huang, Yue Zheng, Feng-Zhu Zhang, Qiu-Fen Sun, Guang Su, Ying-Ying Huang, Shou-Jie Pan, Hui-Rong Wu, Ting Hu, Yue-Mei Zhang, Jun Zhu, Feng-Cai Xia, Ning-Shao Lancet Reg Health West Pac Articles BACKGROUND: A safe and highly efficacious Escherichia coli (E. coli)-produced HPV 16/18 bivalent vaccine has been prequalified by the World Health Organization. Here, we conducted a single-center, open-label, dose-escalation phase 1 clinical trial to evaluate the safety and immunogenicity of the second-generation nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. METHOD: Twenty-four eligible volunteers aged 18–45 years were enrolled in January 2019 in Dongtai, China and received 0.5 mL (135 μg) or 1.0 mL (270 μg) of the candidate vaccine with a 0/1/6-month dose-escalation schedule. Local and systemic adverse events (AEs) occurring within 30 days after each vaccination and serious adverse events (SAEs) occurring within 7 months were recorded. Blood samples from each participant were collected before and 2 days after the first and third vaccinations to determine changes in laboratory parameters. Serum IgG and neutralizing antibody (nAb) levels against each HPV type at month 7 were analyzed (ClinicalTrials.gov: NCT03813940). FINDINGS: The incidences of total AEs in the 135 μg and 270 μg groups were 66.7% and 83.3%, respectively. All AEs were mild or moderate, and no SAEs were reported. No clinically significant changes were found in paired blood indices before or after any of the vaccinations. All the participants in the per-protocol set except for two who failed to seroconvert for HPV 11 or 58 in the 135 μg group seroconverted at month 7 for both IgG and nAbs. INTERPRETATION: The candidate E. coli-produced 9vHPV vaccine has been preliminarily proven to be well tolerated and immunogenic, which encourages further studies in large cohorts with a wider age range. FUNDING: This study was supported by the 10.13039/501100001809National Natural Science Foundation of China, 10.13039/501100003392Fujian Provincial Natural Science Foundation, Fujian Province Health and Education Joint Research Program, Xiamen Science and Technology Plan Project, 10.13039/501100012226Fundamental Research Funds for the Central Universities, 10.13039/501100005150CAMS Innovation Fund for Medical Sciences of China, and Xiamen Innovax Biotechnology Co., Ltd. Elsevier 2023-03-13 /pmc/articles/PMC10240382/ /pubmed/37283969 http://dx.doi.org/10.1016/j.lanwpc.2023.100731 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Chu, Kai
Bi, Zhao-Feng
Huang, Wei-Jin
Li, Ya-Fei
Zhang, Li
Yang, Chang-Lin
Jiang, Han-Min
Zang, Xia
Chen, Qi
Liu, Dong-Lin
Pan, Hong-Xing
Huang, Yue
Zheng, Feng-Zhu
Zhang, Qiu-Fen
Sun, Guang
Su, Ying-Ying
Huang, Shou-Jie
Pan, Hui-Rong
Wu, Ting
Hu, Yue-Mei
Zhang, Jun
Zhu, Feng-Cai
Xia, Ning-Shao
Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title_full Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title_fullStr Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title_full_unstemmed Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title_short Safety and immunogenicity of an Escherichia coli-produced 9-valent human papillomavirus L1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
title_sort safety and immunogenicity of an escherichia coli-produced 9-valent human papillomavirus l1 virus-like particle vaccine (types 6/11/16/18/31/33/45/52/58) in healthy adults: an open-label, dose-escalation phase 1 clinical trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240382/
https://www.ncbi.nlm.nih.gov/pubmed/37283969
http://dx.doi.org/10.1016/j.lanwpc.2023.100731
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