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A multitope SARS-CoV-2 vaccine provides long-lasting B cell and T cell immunity against Delta and Omicron variants.


ABSTRACT: BackgroundThe Delta and Omicron variants of SARS-CoV-2 are currently responsible for breakthrough infections due to waning immunity. We report phase I/II trial results of UB-612, a multitope subunit vaccine containing S1-RBD-sFc protein and rationally designed promiscuous peptides representing sarbecovirus conserved helper T cell and cytotoxic T lymphocyte epitopes on the nucleocapsid (N), membrane (M), and spike (S2) proteins.MethodWe conducted a phase I primary 2-dose (28 days apart) trial of 10, 30, or 100 μg UB-612 in 60 healthy young adults 20 to 55 years old, and 50 of them were boosted with 100 μg of UB-612 approximately 7 to 9 months after the second dose. A separate placebo-controlled and randomized phase II study was conducted with 2 doses of 100 μg of UB-612 (n = 3,875, 18-85 years old). We evaluated interim safety and immunogenicity of phase I until 14 days after the third (booster) dose and of phase II until 28 days after the second dose.ResultsNo vaccine-related serious adverse events were recorded. The most common solicited adverse events were injection site pain and fatigue, mostly mild and transient. In both trials, UB-612 elicited respective neutralizing antibody titers similar to a panel of human convalescent sera. The most striking findings were long-lasting virus-neutralizing antibodies and broad T cell immunity against SARS-CoV-2 variants of concern (VoCs), including Delta and Omicron, and a strong booster-recalled memory immunity with high cross-reactive neutralizing titers against the Delta and Omicron VoCs.ConclusionUB-612 has presented a favorable safety profile, potent booster effect against VoCs, and long-lasting B and broad T cell immunity that warrants further development for both primary immunization and heterologous boosting of other COVID-19 vaccines.Trial RegistrationClinicalTrials.gov: NCT04545749, NCT04773067, and NCT04967742.FundingUBI Asia, Vaxxinity Inc., and Taiwan Centers for Disease Control, Ministry of Health and Welfare.

SUBMITTER: Wang CY 

PROVIDER: S-EPMC9106357 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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A multitope SARS-CoV-2 vaccine provides long-lasting B cell and T cell immunity against Delta and Omicron variants.

Wang Chang Yi CY   Hwang Kao-Pin KP   Kuo Hui-Kai HK   Peng Wen-Jiun WJ   Shen Yea-Huei YH   Kuo Be-Sheng BS   Huang Juin-Hua JH   Liu Hope H   Ho Yu-Hsin YH   Lin Feng F   Ding Shuang S   Liu Zhi Z   Wu Huan-Ting HT   Huang Ching-Tai CT   Lee Yuarn-Jang YJ   Liu Ming-Che MC   Yang Yi-Ching YC   Lu Po-Liang PL   Tsai Hung-Chin HC   Lee Chen-Hsiang CH   Shi Zhi-Yuan ZY   Liu Chun-Eng CE   Liao Chun-Hsing CH   Chang Feng-Yee FY   Chen Hsiang-Cheng HC   Wang Fu-Der FD   Hou Kuo-Liang KL   Cheng Jennifer J   Wang Min-Sheng MS   Yang Ya-Ting YT   Chiu Han-Chen HC   Jiang Ming-Han MH   Shih Hao-Yu HY   Shen Hsuan-Yu HY   Chang Po-Yen PY   Lan Yu-Rou YR   Chen Chi-Tian CT   Lin Yi-Ling YL   Liang Jian-Jong JJ   Liao Chun-Che CC   Chou Yu-Chi YC   Morris Mary Kate MK   Hanson Carl V CV   Guirakhoo Farshad F   Hellerstein Michael M   Yu Hui-Jing HJ   King Chwan-Chuen CC   Kemp Tracy T   Heppner D Gray DG   Monath Thomas P TP  

The Journal of clinical investigation 20220501 10


BackgroundThe Delta and Omicron variants of SARS-CoV-2 are currently responsible for breakthrough infections due to waning immunity. We report phase I/II trial results of UB-612, a multitope subunit vaccine containing S1-RBD-sFc protein and rationally designed promiscuous peptides representing sarbecovirus conserved helper T cell and cytotoxic T lymphocyte epitopes on the nucleocapsid (N), membrane (M), and spike (S2) proteins.MethodWe conducted a phase I primary 2-dose (28 days apart) trial of  ...[more]

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