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

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

COVID-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.

Original languageEnglish
Article number2294860
JournalEmerging Microbes and Infections
Volume13
Issue number1
DOIs
Publication statusPublished - 28 Feb 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • DMAb
  • DNA
  • DNA-encoded monoclonal antibody
  • gene-encoded antibody
  • macaque
  • monoclonal antibody
  • prevention
  • SARS-CoV-2

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