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Reduced neutralization of SARS-CoV-2 B.1.617 variant by inactivated and RBD-subunit vaccine
Jie Hu; Xiao-yu Wei; Jin Xiang; Pai Peng; Feng-li Xu; Kang Wu; Fei-yang Luo; Ai-shun Jin; Liang Fang; Bei-zhong Liu; Kai Wang; Ni Tang; Ailong Huang.
Afiliação
  • Jie Hu; Chongqing Medical University
  • Xiao-yu Wei; Yong-Chuan Hospital of Chongqing Medical University
  • Jin Xiang; Chongqing Medical University
  • Pai Peng; Chongqing Medical University
  • Feng-li Xu; Chongqing Medical University
  • Kang Wu; Chongqing Medical University
  • Fei-yang Luo; Chongqing Medical University
  • Ai-shun Jin; Chongqing Medical University
  • Liang Fang; Yong-Chuan Hospital of Chongqing Medical University
  • Bei-zhong Liu; Yong-Chuan Hospital of Chongqing Medical University
  • Kai Wang; Chongqing Medical University
  • Ni Tang; Chongqing Medical University
  • Ailong Huang; Chongqing Medical University
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-451732
ABSTRACT
Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The Spike protein that mediates coronavirus entry into host cells is a major target for COVID-19 vaccines and antibody therapeutics. However, multiple variants of SARS-CoV-2 have emerged, which may potentially compromise vaccine effectiveness. Using a pseudovirus-based assay, we evaluated SARS-CoV-2 cell entry mediated by the viral Spike B.1.617 and B.1.1.7 variants. We also compared the neutralization ability of monoclonal antibodies from convalescent sera and neutralizing antibodies (NAbs) elicited by CoronaVac (inactivated vaccine) and ZF2001 (RBD-subunit vaccine) against B.1.617 and B.1.1.7 variants. Our results showed that, compared to D614G and B.1.1.7 variants, B.1.617 shows enhanced viral entry and membrane fusion, as well as more resistant to antibody neutralization. These findings have important implications for understanding viral infectivity and for immunization policy against SARS-CoV-2 variants.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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