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An elite broadly neutralizing antibody protects SARS-CoV-2 Omicron variant challenge
Biao Zhou; Runhong Zhou; Jasper Fuk-Woo Chan; Mengxiao Luo; Qiaoli Peng; Shuofeng Yuan; Bobo Wing-Yee Mok; Bohao Chen; Pui Wang; Vincent Kwok-Man Poon; Hin Chu; Chris Chung-Sing Chan; Jessica Oi-Ling Tsang; Chris Chun-Yiu Chan; Ka-Kit Au; Hiu-On Man; Lu Lu; Kelvin Kai-Wang To; Honglin Chen; Kwok-Yung Yuen; Zhiwei Chen.
Affiliation
  • Biao Zhou; The University of Hong Kong
  • Runhong Zhou; The University of Hong Kong
  • Jasper Fuk-Woo Chan; The University of Hong Kong
  • Mengxiao Luo; The University of Hong Kong
  • Qiaoli Peng; The University of Hong Kong
  • Shuofeng Yuan; The University of Hong Kong
  • Bobo Wing-Yee Mok; The University of Hong Kong
  • Bohao Chen; The University of Hong Kong
  • Pui Wang; The University of Hong Kong
  • Vincent Kwok-Man Poon; The University of Hong Kong
  • Hin Chu; The University of Hong Kong
  • Chris Chung-Sing Chan; The University of Hong Kong
  • Jessica Oi-Ling Tsang; The University of Hong Kong
  • Chris Chun-Yiu Chan; The University of Hong Kong
  • Ka-Kit Au; The University of Hong Kong
  • Hiu-On Man; The University of Hong Kong
  • Lu Lu; The University of Hong Kong
  • Kelvin Kai-Wang To; The University of Hong Kong
  • Honglin Chen; The University of Hong Kong
  • Kwok-Yung Yuen; The University of Hong Kong
  • Zhiwei Chen; The University of Hong Kong
Preprint in English | bioRxiv | ID: ppbiorxiv-475037
ABSTRACT
The strikingly high transmissibility and antibody evasion of SARS-CoV-2 Omicron variant have posted great challenges on the efficacy of current vaccines and antibody immunotherapy.Here, we screened 34 BNT162b2-vaccinees and cloned a public broadly neutralizing antibody (bNAb) ZCB11 from an elite vaccinee. ZCB11 neutralized all authentic SARS-CoV-2 variants of concern (VOCs), including Omicron and OmicronR346K with potent IC50 concentrations of 36.8 and 11.7 ng/mL, respectively. Functional analysis demonstrated that ZCB11 targeted viral receptor-binding domain (RBD) and competed strongly with ZB8, a known RBD-specific class II NAb. Pseudovirus-based mapping of 57 naturally occurred single mutations or deletions revealed that only S371L resulted in 11-fold neutralization resistance, but this phenotype was not observed in the Omicron variant. Furthermore,prophylactic ZCB11 administration protected lung infection against both the circulating pandemic Delta and Omicron variants in golden Syrian hamsters. These results demonstrated that vaccine-induced ZCB11 is a promising bNAb for immunotherapy against pandemic SARS-CoV-2 VOCs.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
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