Reference Database

YearReference
2022
Circular RNA vaccines against SARS-CoV-2 and emerging variants.
Qu, Liang
Yi, Zongyi
Shen, Yong
Lin, Liangru
Chen, Feng
Xu, Yiyuan
Wu, Zeguang
Tang, Huixian
Zhang, Xiaoxue
Tian, Feng
Wang, Chunhui
Xiao, Xia
Dong, Xiaojing
Guo, Li
Lu, Shuaiyao
Yang, Chengyun
Tang, Cong
Yang, Yun
Yu, Wenhai
Wang, Junbin
Zhou, Yanan
Huang, Qing
Yisimayi, Ayijiang
Liu, Shuo
Huang, Weijin
Cao, Yunlong
Wang, Youchun
Zhou, Zhuo
Peng, Xiaozhong
Wang, Jianwei
Xie, Xiaoliang Sunney
Wei, Wensheng
Cell 2022 May 12;185(10): 1728-1744.e16
Abstract

As the emerging variants of SARS-CoV-2 continue to drive the worldwide pandemic, there is a constant demand for vaccines that offer more effective and broad-spectrum protection. Here, we report a circular RNA (circRNA) vaccine that elicited potent neutralizing antibodies and T cell responses by expressing the trimeric RBD of the spike protein, providing robust protection against SARS-CoV-2 in both mice and rhesus macaques. Notably, the circRNA vaccine enabled higher and more durable antigen production than the 1mΨ-modified mRNA vaccine and elicited a higher proportion of neutralizing antibodies and distinct Th1-skewed immune responses. Importantly, we found that the circRNA vaccine induced effective neutralizing antibodies against the Omicron but not the Delta variant. In contrast, the circRNA vaccine protected against both Delta and Omicron or functioned as a booster after two doses of either native- or Delta-specific vaccination, making it a favorable choice against the current variants of concern (VOCs) of SARS-CoV-2.

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