Development of a multi-antigenic SARS-CoV-2 vaccine candidate using a synthetic poxvirus platform

利用合成痘病毒平台开发多抗原SARS-CoV-2候选疫苗

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作者:Flavia Chiuppesi,Marcela d'Alincourt Salazar,Heidi Contreras,Vu H Nguyen,Joy Martinez,Yoonsuh Park,Jenny Nguyen,Mindy Kha,Angelina Iniguez,Qiao Zhou,Teodora Kaltcheva,Roman Levytskyy,Nancy D Ebelt,Tae Hyuk Kang,Xiwei Wu,Thomas F Rogers,Edwin R Manuel,Yuriy Shostak,Don J Diamond,Felix Wussow

Abstract

Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We demonstrate the construction of a 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 use this 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. We show that mice immunized with these sMVA vectors develop robust SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent neutralizing antibodies. These results demonstrate the potential of a 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.

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