Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform.
Flavia ChiuppesiMarcela d'Alincourt SalazarHeidi ContrerasVu NguyenJoy MartinezSoojin ParkJenny NguyenMindy KhaAngelina IniguezQiao ZhouTeodora KaltchevaRoman LevytskyyNancy Danielle EbeltTae KangXiwei WuTom RogersEdwin ManuelYuriy ShostakDon J DiamondFelix WussowPublished in: Research square (2020)
Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We developed a novel vaccine platform based on a unique three-plasmid system to efficiently generate recombinant MVA vectors from chemically synthesized DNA. In response to the ongoing global pandemic caused by SARS coronavirus-2 (SARS-CoV-2), we used this novel vaccine platform to rapidly produce fully synthetic MVA (sMVA) vectors co-expressing SARS-CoV-2 spike and nucleocapsid antigens, two immunodominant antigens implicated in protective immunity. Mice immunized with these sMVA vectors developed robust SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent neutralizing antibodies. These results demonstrate the potential of a novel vaccine platform based on synthetic DNA to efficiently generate recombinant MVA vectors and to rapidly develop a multi-antigenic poxvirus-based SARS-CoV-2 vaccine candidate.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- immune response
- high throughput
- cell free
- infectious diseases
- gene therapy
- dendritic cells
- circulating tumor
- escherichia coli
- type diabetes
- squamous cell carcinoma
- metabolic syndrome
- coronavirus disease
- crispr cas
- skeletal muscle
- climate change
- papillary thyroid
- insulin resistance
- inflammatory response