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

免疫原性 免疫 病毒学 表位 细胞毒性T细胞 中和抗体 免疫学 抗体 T细胞 医学 细胞免疫 效价 疫苗试验 不利影响 生物 B细胞 体液免疫 抗体效价 启动(农业) 细胞免疫 T淋巴细胞 免疫系统 接种疫苗
作者
Chang Yi Wang,Kao-Pin Hwang,Hui-Kai Kuo,Wen-Jiun Peng,Yea-Huei Shen,Be-Sheng Kuo,Juin-Hua Huang,Hope Liu,Yu-Hsin Ho,Feng Lin,Shuang Ding,Zhi Liu,Huan-Ting Wu,Ching-Tai Huang,Yuarn-Jang Lee,Ming-Che Liu,Yi-Ching Yang,Po-Liang Lu,Hung-Chin Tsai,Chen-Hsiang Lee
出处
期刊:Journal of Clinical Investigation [American Society for Clinical Investigation]
卷期号:132 (10) 被引量:75
标识
DOI:10.1172/jci157707
摘要

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.
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