Q1 · CROSS-FIELD
ArticleOA
Author: Wu, Xiwei ; Rogers, Thomas F ; Iniguez, Angelina ; Manuel, Edwin R ; Ebelt, Nancy D ; Diamond, Don J ; Nguyen, Jenny ; Zhou, Qiao ; Salazar, Marcela d'Alincourt ; Shostak, Yuriy ; Martinez, Joy ; Chiuppesi, Flavia ; Kang, Tae Hyuk ; Nguyen, Vu H ; Levytskyy, Roman ; Kha, Mindy ; Kaltcheva, Teodora ; Contreras, Heidi ; Park, Yoonsuh ; Wussow, Felix
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.