In vivo delivery of engineered synthetic DNA-encoded SARS-CoV-2 monoclonal antibodies for pre-exposure prophylaxis in non-human primates.
Ami PatelKyle RosenkeElizabeth M ParzychFriederike FeldmannSuman BhartiAmanda J GriffinBlake SchouestMatt LewisJihae ChoiNeethu ChokkalingamViviane MachadoBrian J SmithDrew FraseAli R AliJamie LovaglioBrian NguyenPatrick W HanleySusanne N WalkerEbony N GaryAbhijeet KulkarniAllison GenerottiJoseph R FrancicaKim RosenthalDaniel W KulpMark T EsserTrevor R F SmithCarl I ShaiaDavid B WeinerHeinrich FeldmannPublished in: Emerging microbes & infections (2024)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- public health
- low dose
- cell free
- circulating tumor
- infectious diseases
- coronavirus disease
- single molecule
- binding protein
- healthcare
- poor prognosis
- copy number
- emergency department
- big data
- dna methylation
- genome wide
- artificial intelligence
- machine learning
- gene expression
- early onset
- small molecule
- induced pluripotent stem cells
- nucleic acid
- long non coding rna
- protein protein