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Development of a Multi-Antigenic SARS-CoV-2 Vaccine Using a Synthetic Poxvirus Platform.
Chiuppesi, Flavia; Salazar, Marcela d'Alincourt; Contreras, Heidi; Nguyen, Vu; Martinez, Joy; Park, Soojin; Nguyen, Jenny; Kha, Mindy; Iniguez, Angelina; Zhou, Qiao; Kaltcheva, Teodora; Levytskyy, Roman; Ebelt, Nancy; Kang, Tae; Wu, Xiwei; Rogers, Tom; Manuel, Edwin; Shostak, Yuriy; Diamond, Don; Wussow, Felix.
Affiliation
  • Chiuppesi F; City Of Hope National Medical Center.
  • Salazar MD; City of Hope.
  • Contreras H; City of Hope.
  • Nguyen V; City of Hope.
  • Martinez J; City of Hope.
  • Park S; City of Hope.
  • Nguyen J; City of Hope.
  • Kha M; City of Hope.
  • Iniguez A; City of Hope.
  • Zhou Q; City of Hope.
  • Kaltcheva T; City of Hope.
  • Levytskyy R; City of Hope.
  • Ebelt N; Beckman Research Institute of City of Hope.
  • Kang T; Beckman Research Institute of City of Hope.
  • Wu X; Beckman Research Institute of City of Hope.
  • Rogers T; University of California San Diego.
  • Manuel E; City Of Hope National Medical Center.
  • Shostak Y; City of Hope.
  • Diamond D; City of Hope.
  • Wussow F; City of Hope.
Res Sq ; 2020 Jul 17.
Article in En | MEDLINE | ID: mdl-32702732
ABSTRACT
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Res Sq Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Res Sq Year: 2020 Document type: Article