4.7 Article

Isolation of a panel of ultra-potent human antibodies neutralizing SARS-CoV-2 and viral variants of concern

Journal

CELL DISCOVERY
Volume 7, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41421-021-00340-8

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Funding

  1. Russian Fund of Basic Research (RFBR) [20-04-60527]
  2. RFBR [18-29-08051]
  3. Basic scientific research program [0246-2021-0016]
  4. Russian Ministry of Science and Higher Education of the Russian Federation [075-15-2019-1660]

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In the absence of approved small-molecule drugs targeting the virus, broadening the repertoire of potent SARS-CoV-2-neutralizing antibodies is crucial. This study isolated 23 RBD-specific human monoclonal antibodies with strong virus-neutralizing activity, including four categorized as ultrapotent. These antibodies retain activity against various SARS-CoV-2 variants and could effectively prevent viral replication and lung pathology.
In the absence of virus-targeting small-molecule drugs approved for the treatment and prevention of COVID-19, broadening the repertoire of potent SARS-CoV-2-neutralizing antibodies represents an important area of research in response to the ongoing pandemic. Systematic analysis of such antibodies and their combinations can be particularly instrumental for identification of candidates that may prove resistant to the emerging viral escape variants. Here, we isolated a panel of 23 RBD-specific human monoclonal antibodies from the B cells of convalescent patients. A surprisingly large proportion of such antibodies displayed potent virus-neutralizing activity both in vitro and in vivo. Four of the isolated nAbs can be categorized as ultrapotent with an apparent IC100 below 16 ng/mL. We show that individual nAbs as well as dual combinations thereof retain activity against currently circulating SARS-CoV-2 variants of concern (such as B.1.1.7, B.1.351, B.1.617, and C.37), as well as against other viral variants. When used as a prophylactics or therapeutics, these nAbs could potently suppress viral replication and prevent lung pathology in SARS-CoV-2-infected hamsters. Our data contribute to the rational development of oligoclonal therapeutic nAb cocktails mitigating the risk of SARS-CoV-2 escape.

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