TitleCircular RNA vaccines against SARS-CoV-2 and emerging variants
AuthorsQu, 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
AffiliationPeking 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
KeywordsANTIBODY-DEPENDENT ENHANCEMENT
POTENT
INFECTION
IMMUNOGENICITY
COVID-19
DESIGN
DRIVEN
SAFETY
ACE2
Issue Date12-May-2022
PublisherCELL
AbstractAs 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.
URIhttp://hdl.handle.net/20.500.11897/647131
ISSN0092-8674
DOI10.1016/j.cell.2022.03.044
IndexedSCI(E)
Appears in Collections:生命科学学院
前沿交叉学科研究院

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