De Novo Human Angiotensin-Converting Enzyme 2 Decoy NL-CVX1 Protects Mice From Severe Disease After Severe Acute Respiratory Syndrome Coronavirus 2 Infection.
Maria RebeloCong TangAna R CoelhoCarlos Labão-AlmeidaMatthias M SchneiderLaurie TatalickPedro RuivoMarta Pires de MirandaAndreia GomesTânia CarvalhoMatthew J WalkerHannes AusserwoegerJ Pedro SimasMarc VeldhoenTuomas P J KnowlesDaniel-Adriano SilvaDavid ShoultzGonçalo J L BernardesPublished in: The Journal of infectious diseases (2023)
The emergence of novel variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) underscores the need to investigate alternative approaches to prevent infection and treat patients with coronavirus disease 2019. Here, we report the preclinical efficacy of NL-CVX1, a de novo decoy that blocks virus entry into cells by binding with nanomolar affinity and high specificity to the receptor-binding domain of the SARS-CoV-2 spike protein. Using a transgenic mouse model of SARS-CoV-2 infection, we showed that a single prophylactic intranasal dose of NL-CVX1 conferred complete protection from severe disease following SARS-CoV-2 infection. Multiple therapeutic administrations of NL-CVX1 also protected mice from succumbing to infection. Finally, we showed that infected mice treated with NL-CVX1 developed both anti-SARS-CoV-2 antibodies and memory T cells and were protected against reinfection a month after treatment. Overall, these observations suggest NL-CVX1 is a promising therapeutic candidate for preventing and treating severe SARS-CoV-2 infections.
Keyphrases
- respiratory syndrome coronavirus
- sars cov
- coronavirus disease
- angiotensin converting enzyme
- high fat diet induced
- mouse model
- early onset
- angiotensin ii
- binding protein
- endothelial cells
- wild type
- type diabetes
- stem cells
- small molecule
- oxidative stress
- working memory
- endoplasmic reticulum stress
- induced pluripotent stem cells
- bone marrow
- skeletal muscle
- protein protein
- mesenchymal stem cells
- capillary electrophoresis