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dc.creatorLien, Chia-En
dc.creatorLiu, Ming-Che
dc.creatorWang, Ning-Chi
dc.creatorLiu, Luke Tzu-Chi
dc.creatorWu, Chung-Chin
dc.creatorTang, Wei-Hsuan
dc.creatorLian, Wei-Cheng
dc.creatorHuang, Kuan-Ying A.
dc.creatorChen, Charles
dc.date.accessioned2022-12-20T19:23:39Z
dc.date.available2022-12-20T19:23:39Z
dc.date.issued2022-08-31
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/8184
dc.identifier.urihttp://hdl.handle.net/20.500.12613/8213
dc.description.abstractBackground: 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.extent30 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofCOVID-19 Research
dc.relation.isreferencedbymedRxiv
dc.rightsAttribution-NonCommercial-NoDerivs CC BY-NC-ND
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectSARS-CoV-2 vaccine
dc.subjectMVC-COV1901
dc.subjectBooster vaccination
dc.subjectSARS-CoV-2 Beta variant booster vaccine
dc.subjectOmicron variant
dc.titleA 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.typeText
dc.type.genrePre-print
dc.description.departmentBiology
dc.relation.doihttps://doi.org/10.1101/2022.08.29.22279317
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeTemple University. College of Science and Technology
dc.creator.orcidChen|0000-0001-6888-009X
dc.temple.creatorChen, Charles
refterms.dateFOA2022-12-20T19:23:39Z


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