Literature DB >> 32714117

Neutralizing Antibody and Soluble ACE2 Inhibition of a Replication-Competent VSV-SARS-CoV-2 and a Clinical Isolate of SARS-CoV-2.

James Brett Case1, Paul W Rothlauf2,3, Rita E Chen1,4, Zhuoming Liu2, Haiyan Zhao5, Arthur S Kim1,4, Louis-Marie Bloyet2, Qiru Zeng2, Stephen Tahan2, Lindsay Droit2, Ma Xenia G Ilagan5, Michael A Tartell2,3, Gaya Amarasinghe2,4,5, Jeffrey P Henderson1, Shane Miersch6, Mart Ustav6, Sachdev Sidhu6, Herbert W Virgin7, David Wang2, Siyuan Ding2, Davide Corti8, Elitza S Theel9, Daved H Fremont2,4,5,10, Michael S Diamond1,2,5,10, Sean P J Whelan2.   

Abstract

Antibody-based interventions against SARS-CoV-2 could limit morbidity, mortality, and possibly disrupt epidemic transmission. An anticipated correlate of such countermeasures is the level of neutralizing antibodies against the SARS-CoV-2 spike protein, yet there is no consensus as to which assay should be used for such measurements. Using an infectious molecular clone of vesicular stomatitis virus (VSV) that expresses eGFP as a marker of infection, we replaced the glycoprotein gene (G) with the spike protein of SARS-CoV-2 (VSV-eGFP-SARS-CoV-2) and developed a high-throughput imaging-based neutralization assay at biosafety level 2. We also developed a focus reduction neutralization test with a clinical isolate of SARS-CoV-2 at biosafety level 3. We compared the neutralizing activities of monoclonal and polyclonal antibody preparations, as well as ACE2-Fc soluble decoy protein in both assays and find an exceptionally high degree of concordance. The two assays will help define correlates of protection for antibody-based countermeasures including therapeutic antibodies, immune γ-globulin or plasma preparations, and vaccines against SARS-CoV-2. Replication-competent VSV-eGFP-SARS-CoV-2 provides a rapid assay for testing inhibitors of SARS-CoV-2 mediated entry that can be performed in 7.5 hours under reduced biosafety containment. Funding: This study was supported by NIH contracts and grants (75N93019C00062, HHSN272201700060C and R01 AI127828, R37 AI059371 and U01 AI151810) and the Defense Advanced Research Project Agency (HR001117S0019) and gifts from Washington University in Saint Louis. J.B.C. is supported by a Helen Hay Whitney Foundation postdoctoral fellowship. Conflict of Interest: M.S.D. is a consultant for Inbios, Vir Biotechnology, NGM Biopharmaceuticals, and on the Scientific Advisory Board of Moderna. D.C. and H.W.V. are employees of Vir Biotechnology Inc. and may hold shares in Vir Biotechnology Inc. S.P.J.W. and P.W.R. have filed a disclosure with Washington University for the recombinant VSV. Ethical Approval: This study was approved by the Mayo Clinic Institutional Review Board.

Entities:  

Keywords:  Neutralization Assay; SARS-CoV-2; coronavirus spike; vesicular stomatitis virus

Year:  2020        PMID: 32714117      PMCID: PMC7366811          DOI: 10.2139/ssrn.3606354

Source DB:  PubMed          Journal:  SSRN        ISSN: 1556-5068


  1 in total

1.  A Net Benefit Approach for the Optimal Allocation of a COVID-19 Vaccine.

Authors:  Erin Kirwin; Ellen Rafferty; Kate Harback; Jeff Round; Christopher McCabe
Journal:  Pharmacoeconomics       Date:  2021-06-17       Impact factor: 4.981

  1 in total

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