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Development of potent and effective synthetic SARS-CoV-2 neutralizing nanobodies.
Stefan, Maxwell A; Light, Yooli K; Schwedler, Jennifer L; McIlroy, Peter R; Courtney, Colleen M; Saada, Edwin A; Thatcher, Christine E; Phillips, Ashlee M; Bourguet, Feliza A; Mageeney, Catherine M; McCloy, Summer A; Collette, Nicole M; Negrete, Oscar A; Schoeniger, Joseph S; Weilhammer, Dina R; Harmon, Brooke.
Afiliação
  • Stefan MA; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
  • Light YK; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
  • Schwedler JL; Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, USA.
  • McIlroy PR; Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, USA.
  • Courtney CM; Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, USA.
  • Saada EA; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
  • Thatcher CE; Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, USA.
  • Phillips AM; Biosciences and Biotechnology Division, Lawrence Livermore National Laboratories, Livermore, USA.
  • Bourguet FA; Biosciences and Biotechnology Division, Lawrence Livermore National Laboratories, Livermore, USA.
  • Mageeney CM; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
  • McCloy SA; Biosciences and Biotechnology Division, Lawrence Livermore National Laboratories, Livermore, USA.
  • Collette NM; Biosciences and Biotechnology Division, Lawrence Livermore National Laboratories, Livermore, USA.
  • Negrete OA; Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, USA.
  • Schoeniger JS; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
  • Weilhammer DR; Biosciences and Biotechnology Division, Lawrence Livermore National Laboratories, Livermore, USA.
  • Harmon B; Systems Biology Department, Sandia National Laboratories, Livermore, USA.
MAbs ; 13(1): 1958663, 2021.
Article em En | MEDLINE | ID: mdl-34348076
ABSTRACT
The respiratory virus responsible for coronavirus disease 2019 (COVID-19), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has affected nearly every aspect of life worldwide, claiming the lives of over 3.9 million people globally, at the time of this publication. Neutralizing humanized nanobody (VHH)-based antibodies (VHH-huFc) represent a promising therapeutic intervention strategy to address the current SARS-CoV-2 pandemic and provide a powerful toolkit to address future virus outbreaks. Using a synthetic, high-diversity VHH bacteriophage library, several potent neutralizing VHH-huFc antibodies were identified and evaluated for their capacity to tightly bind to the SARS-CoV-2 receptor-binding domain, to prevent binding of SARS-CoV-2 spike (S) to the cellular receptor angiotensin-converting enzyme 2, and to neutralize viral infection. Preliminary preclinical evaluation of multiple VHH-huFc antibody candidates demonstrate that they are prophylactically and therapeutically effective in vivo against wildtype SARS-CoV-2. The identified and characterized VHH-huFc antibodies described herein represent viable candidates for further preclinical evaluation and another tool to add to our therapeutic arsenal to address the COVID-19 pandemic.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anticorpos Neutralizantes / Anticorpos de Domínio Único / SARS-CoV-2 / COVID-19 / Anticorpos Antivirais Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anticorpos Neutralizantes / Anticorpos de Domínio Único / SARS-CoV-2 / COVID-19 / Anticorpos Antivirais Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article