Title | Circular RNA vaccines against SARS-CoV-2 and emerging variants |
Authors | 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 |
Affiliation | Peking Univ, Peking Univ Genome Editing Res Ctr,Peking Tsinghu, Sch Life Sci,Beijing Adv Innovat Ctr Genom, State Key Lab Prot & Plant Gene Res,Biomed Pionee, Beijing 100871, Peoples R China Peking Univ, Acad Adv Interdisciplinary Studies, Beijing 100871, Peoples R China Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, NHC Key Lab Syst Biol Pathogens, Beijing 100730, Peoples R China Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, Christophe Merieux Lab, Beijing 100730, Peoples R China Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biol, Natl Kunming High Level Biosafety Primate Res Ctr, Kunming, Yunnan, Peoples R China Peking Univ, Biomed Pioneering Innovat Ctr, Beijing Adv Innovat Ctr Genom, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China Natl Inst Food & Drug Control NIFDC, Inst Biol Prod Control, Div HIV AIDS & Sex Transmitted Virus Vaccines, Beijing 102629, Peoples R China WHO Collaborating Ctr Standardizat & Evaluat Biol, Beijing 102629, Peoples R China Chinese Acad Med Sci, Sch Basic Med,Dept Mol Biol & Biochem, Peking Union Med Coll,State Key Lab Med Mol Biol, Med Primate Res Ctr,Neurosci Ctr,Inst Basic Med S, Beijing 100730, Peoples R China Chinese Acad Med Sci & Peking Union Med Coll, Key Lab Resp Dis Pathogen, Beijing 100730, Peoples R China |
Keywords | ANTIBODY-DEPENDENT ENHANCEMENT POTENT INFECTION IMMUNOGENICITY COVID-19 DESIGN DRIVEN SAFETY ACE2 |
Issue Date | 12-May-2022 |
Publisher | CELL |
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 1m Psi-modified mRNA vaccine and elicited a higher proportion of neutralizing antibodies and distinct Th1-skewed immune responses. Importantly, we found that the circRNA(RBD)(-Omicron) vaccine induced effective neutralizing antibodies against the Omicron but not the Delta variant. In contrast, the circRNA(RBD)(-Delta) 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. |
URI | http://hdl.handle.net/20.500.11897/647131 |
ISSN | 0092-8674 |
DOI | 10.1016/j.cell.2022.03.044 |
Indexed | SCI(E) |
Appears in Collections: | 生命科学学院 前沿交叉学科研究院 |