A Phase I, Prospective, Randomized, Open-labeled Study to Evaluate the Safety, Tolerability, and Immunogenicity of Booster Dose with MVC-COV1901 or MVC-COV1901(Beta) SARS-CoV-2 Vaccine in Adults
dc.creator | Lien, Chia-En | |
dc.creator | Liu, Ming-Che | |
dc.creator | Wang, Ning-Chi | |
dc.creator | Liu, Luke Tzu-Chi | |
dc.creator | Wu, Chung-Chin | |
dc.creator | Tang, Wei-Hsuan | |
dc.creator | Lian, Wei-Cheng | |
dc.creator | Huang, Kuan-Ying A. | |
dc.creator | Chen, Charles | |
dc.date.accessioned | 2022-12-20T19:23:39Z | |
dc.date.available | 2022-12-20T19:23:39Z | |
dc.date.issued | 2022-08-31 | |
dc.identifier.doi | http://dx.doi.org/10.34944/dspace/8184 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12613/8213 | |
dc.description.abstract | Background: The use of variant-based severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine as a booster is being evaluated to overcome reduced neutralisation of variants induced by the original SARS-CoV-2 vaccine and waning protection over time. Methods: This is a phase one, prospective, randomized, and open-labeled trial to study the safety and immunogenicity of a booster dose consisting of a subunit vaccine based on the stabilized prefusion SARS-CoV-2 spike protein, MVC-COV1901 or its Beta version, MVC-COV1901-Beta. One-hundred and seven participants aged ≥18 and <55 years, who received two or three prior doses of MVC-COV1901 vaccines, were enrolled and were to receive a booster dose of either 15 mcg of MVC-COV1901, 15 mcg or 25 mcg of MVC-COV1901-Beta in 1:1:1 ratio. The primary endpoints were the incidences of adverse events and immunogenicity of the booster dose from Visit 2 (the day of the booster) to Visit 5 (four weeks after the booster). Cellular immunity was also investigated with memory B cell (MBC) and T cell assays. Findings: Adverse reactions after either MVC-COV1901 or MVC-COV1901-Beta booster doses after two or three doses of MVC-COV1901 were comparable and mostly mild and transient. At four weeks after the booster dose, participants with two prior doses of MVC-COV1901 exhibited numerically higher levels of neutralising antibodies against SARS-CoV-2 or Beta variant than participants with three prior doses of MVC-COV1901 regardless of the type of booster used. However, compared to 15 mcg of MVC-COV1901, 25 mcg of MVC-COV1901-Beta significantly improved neutralising antibody titre against Beta variant and BA.4/BA.5 Omicron variant pseudoviruses. The booster dose also significantly increased the proportion of spike-specific MBCs, including those of Beta and Omicron variants. Interpretation: MVC-COV1901-Beta can be effectively used as a booster dose against SARS-CoV-2, including the circulating BA.4/BA.5 Omicron variant. | |
dc.format.extent | 30 pages | |
dc.language | English | |
dc.language.iso | eng | |
dc.relation.ispartof | COVID-19 Research | |
dc.relation.isreferencedby | medRxiv | |
dc.rights | Attribution-NonCommercial-NoDerivs CC BY-NC-ND | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | COVID-19 | |
dc.subject | SARS-CoV-2 | |
dc.subject | SARS-CoV-2 vaccine | |
dc.subject | MVC-COV1901 | |
dc.subject | Booster vaccination | |
dc.subject | SARS-CoV-2 Beta variant booster vaccine | |
dc.subject | Omicron variant | |
dc.title | A Phase I, Prospective, Randomized, Open-labeled Study to Evaluate the Safety, Tolerability, and Immunogenicity of Booster Dose with MVC-COV1901 or MVC-COV1901(Beta) SARS-CoV-2 Vaccine in Adults | |
dc.type | Text | |
dc.type.genre | Pre-print | |
dc.description.department | Biology | |
dc.relation.doi | https://doi.org/10.1101/2022.08.29.22279317 | |
dc.ada.note | For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu | |
dc.description.schoolcollege | Temple University. College of Science and Technology | |
dc.creator.orcid | Chen|0000-0001-6888-009X | |
dc.temple.creator | Chen, Charles | |
refterms.dateFOA | 2022-12-20T19:23:39Z |