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Generation and characterization of humanized synergistic neutralizing antibodies against SARS-CoV-2.
Guo, Jiazheng; Zhang, Jun; Du, Peng; Lu, Jiansheng; Chen, Lei; Huang, Ying; Yu, Yunzhou; Xie, Qing; Wang, Rong; Yang, Zhixin.
  • Guo J; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Zhang J; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Du P; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Lu J; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Chen L; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Huang Y; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Yu Y; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Xie Q; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Wang R; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
  • Yang Z; Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
J Med Virol ; 94(8): 3791-3800, 2022 08.
Article in English | MEDLINE | ID: covidwho-1802449
ABSTRACT
The emerging coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the causative agent of coronavirus disease 2019 (COVID-19), which has become a severe threat to global public health and local economies. In this study, several single-chain antibody fragments that bind to the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein were identified and used to construct human-mouse chimeric antibodies and humanized antibodies. These antibodies exhibited strong binding to RBD and neutralization activity towards a SARS-CoV-2 pseudovirus. Moreover, these antibodies recognize different RBD epitopes and exhibit synergistic neutralizing activity. These provide candidate to combination use or bispecific antibody to potential clinical therapy for COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: J Med Virol Year: 2022 Document Type: Article Affiliation country: Jmv.27801

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: J Med Virol Year: 2022 Document Type: Article Affiliation country: Jmv.27801