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Safety and immunogenicity of a pichia pastoris-expressed bivalent human papillomavirus (types 16 and 18) L1 virus-like particle vaccine in healthy Chinese women aged 9-45 years: A randomized, double-blind, placebo-controlled phase 1 clinical trial.
- Source :
-
Vaccine [Vaccine] 2023 May 05; Vol. 41 (19), pp. 3141-3149. Date of Electronic Publication: 2023 Apr 13. - Publication Year :
- 2023
-
Abstract
- Background: We evaluated the safety and immunogenicity of high and low doses of a novel pichia pastoris-expressed bivalent (types 16 and 18) human papillomavirus (HPV) virus-like particle vaccine.<br />Methods: In this randomized, double-blind, placebo-controlled phase 1 trial, we enrolled 160 healthy females aged 9-45 years in Guangxi, China who were randomized (1:1:2) to receive either low (0.5 mL) or high (1.0 mL) dosages of bivalent HPV vaccine, or placebo (aluminum adjuvant) in a 0, 2, 6 months schedule. Adverse events and other significant conditions that occurred within 30 days after each vaccination were recorded throughout the trial. Sera were collected at days 0, 60, 180 and 210 to measure anti-HPV 16/18 neutralizing antibodies.<br />Results: A total of 160 participants received at least one dose of the HPV vaccine and 152 completed the three dose vaccination series. Reporting rates of adverse events in placebo, low dose (0.5 mL) and high dose (1.0 mL) groups were 47.5 %, 55.0 % and 55.0 %, respectively. No serious adverse events occurred during this trial. 100 % of the participants who received three doses of the HPV vaccine produced neutralizing antibodies against HPV 16/18 vaccine. For HPV 16 and HPV 18, the geometric mean titers (GMTs) were similar between the low dose group (GMT <subscript>HPV 16</subscript>  = 10816 [95 % CI: 7824-14953]), GMT <subscript>HPV 18</subscript>  = 3966 [95 % CI: 2693-5841]) and high dose group (GMT <subscript>HPV 16</subscript>  = 14482 [95 % CI: 10848-19333], GMT <subscript>HPV 18</subscript>  = 3428 [95 % CI: 2533-4639]).<br />Conclusion: The pichia pastoris-expressed bivalent HPV vaccine was safe and immunogenic in Chinese females aged 9-45 years. The low dosage (0.5 mL) was selected for further immunogenicity and efficacy study.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: B-W Yu, L-Y Zhou and L Shi were full-time employees of the manufacturer at the time of the study, other authors declare no conflicts of interest.<br /> (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
- Subjects :
- Female
Humans
Antibodies, Neutralizing
Antibodies, Viral
China
Double-Blind Method
East Asian People
Human Papillomavirus Viruses
Immunogenicity, Vaccine
Papillomaviridae
Child
Adolescent
Young Adult
Adult
Middle Aged
Papillomavirus Infections prevention & control
Papillomavirus Vaccines
Vaccines, Virus-Like Particle adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-2518
- Volume :
- 41
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Vaccine
- Publication Type :
- Academic Journal
- Accession number :
- 37061370
- Full Text :
- https://doi.org/10.1016/j.vaccine.2023.04.009