Emerging Microbes and Infections (Dec 2024)

In vivo delivery of engineered synthetic DNA-encoded SARS-CoV-2 monoclonal antibodies for pre-exposure prophylaxis in non-human primates

  • Ami Patel,
  • Kyle Rosenke,
  • Elizabeth M. Parzych,
  • Friederike Feldmann,
  • Suman Bharti,
  • Amanda J. Griffin,
  • Blake Schouest,
  • Matt Lewis,
  • Jihae Choi,
  • Neethu Chokkalingam,
  • Viviane Machado,
  • Brian J. Smith,
  • Drew Frase,
  • Ali R. Ali,
  • Jamie Lovaglio,
  • Brian Nguyen,
  • Patrick W. Hanley,
  • Susanne N. Walker,
  • Ebony N. Gary,
  • Abhijeet Kulkarni,
  • Allison Generotti,
  • Joseph R. Francica,
  • Kim Rosenthal,
  • Daniel W. Kulp,
  • Mark T. Esser,
  • Trevor R. F. Smith,
  • Carl Shaia,
  • David B. Weiner,
  • Heinz Feldmann

DOI
https://doi.org/10.1080/22221751.2023.2294860
Journal volume & issue
Vol. 13, no. 1

Abstract

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ABSTRACTCOVID-19 remains a major public health concern. Monoclonal antibodies have received emergency use authorization (EUA) for pre-exposure prophylaxis against COVID-19 among high-risk groups for treatment of mild to moderate COVID-19. In addition to recombinant biologics, engineered synthetic DNA-encoded antibodies (DMAb) are an important strategy for direct in vivo delivery of protective mAb. A DMAb cocktail was synthetically engineered to encode the immunoglobulin heavy and light chains of two different two different Fc-engineered anti-SARS-CoV-2 antibodies. The DMAbs were designed to enhance in vivo expression and delivered intramuscularly to cynomolgus and rhesus macaques with a modified in vivo delivery regimen. Serum levels were detected in macaques, along with specific binding to SARS-CoV-2 spike receptor binding domain protein and neutralization of multiple SARS-CoV-2 variants of concern in pseudovirus and authentic live virus assays. Prophylactic administration was protective in rhesus macaques against signs of SARS-CoV-2 (USA-WA1/2020) associated disease in the lungs. Overall, the data support further study of DNA-encoded antibodies as an additional delivery mode for prevention of COVID-19 severe disease. These data have implications for human translation of gene-encoded mAbs for emerging infectious diseases and low dose mAb delivery against COVID-19.

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