Back to Search Start Over

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

Authors :
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
Zhi-Yuan Shi
Chun-Eng Liu
Chun-Hsing Liao
Feng-Yee Chang
Hsiang-Cheng Chen
Fu-Der Wang
Kuo-Liang Hou
Jennifer Cheng
Min-Sheng Wang
Ya-Ting Yang
Han-Chen Chiu
Ming-Han Jiang
Hao-Yu Shih
Hsuan-Yu Shen
Po-Yen Chang
Yu-Rou Lan
Chi-Tian Chen
Yi-Ling Lin
Jian-Jong Liang
Chun-Che Liao
Yu-Chi Chou
Mary Kate Morris
Carl V. Hanson
Farshad Guirakhoo
Michael Hellerstein
Hui-Jing Yu
Chwan-Chuen King
Tracy Kemp
D. Gray Heppner
Thomas P. Monath
Source :
The Journal of Clinical Investigation, Vol 132, Iss 10 (2022)
Publication Year :
2022
Publisher :
American Society for Clinical Investigation, 2022.

Abstract

Background The 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.Method We 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.Results No 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.Conclusion UB-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 Registration ClinicalTrials.gov: NCT04545749, NCT04773067, and NCT04967742.Funding UBI Asia, Vaxxinity Inc., and Taiwan Centers for Disease Control, Ministry of Health and Welfare.

Subjects

Subjects :
COVID-19
Medicine

Details

Language :
English
ISSN :
15588238
Volume :
132
Issue :
10
Database :
Directory of Open Access Journals
Journal :
The Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsdoj.6d6f293c98474b5f96a331e81908a684
Document Type :
article
Full Text :
https://doi.org/10.1172/JCI157707