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Fast-Track Discovery of SARS-CoV-2-Neutralizing Antibodies from Human B Cells by Direct Functional Screening.

Matthias HillenbrandChristoph EsslingerJemima SeidenbergMarcel WeberAndreas ZinggCatherine TownsendBarbara EicherJustina RutkauskaitePeggy RieseCarlos Alberto GuzmánKarsten FischerSimone Schmitt
Published in: Viruses (2024)
As the COVID-19 pandemic revealed, rapid development of vaccines and therapeutic antibodies are crucial to guarantee a quick return to the status quo of society. In early 2020, we deployed our droplet microfluidic single-cell-based platform DROPZYLLA ® for the generation of cognate antibody repertoires of convalescent COVID-19 donors. Discovery of SARS-CoV-2-specific antibodies was performed upon display of antibodies on the surface of HEK293T cells by antigen-specific sorting using binding to the SARS-CoV-2 spike and absence of binding to huACE2 as the sort criteria. This efficiently yielded antibodies within 3-6 weeks, of which up to 100% were neutralizing. One of these, MTX-COVAB, displaying low picomolar neutralization IC50 of SARS-CoV-2 and with a neutralization potency on par with the Regeneron antibodies, was selected for GMP manufacturing and clinical development in June 2020. MTX-COVAB showed strong efficacy in vivo and neutralized all identified clinically relevant variants of SARS-CoV-2 at the time of its selection. MTX-COVAB completed GMP manufacturing by the end of 2020, but clinical development was stopped when the Omicron variant emerged, a variant that proved to be detrimental to all monoclonal antibodies already approved. The present study describes the capabilities of the DROPZYLLA ® platform to identify antibodies of high virus-neutralizing capacity rapidly and directly.
Keyphrases
  • sars cov
  • single cell
  • high throughput
  • respiratory syndrome coronavirus
  • small molecule
  • rna seq
  • endothelial cells
  • cystic fibrosis
  • quantum dots
  • gestational age