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Development of a Synthetic Poxvirus-Based SARS-CoV-2 Vaccine
Flavia Chiuppesi; Marcela Salazar Werner; Heidi Contreras; Hong Vu Nguyen; Joy Martinez; Soojin Park; Jenny Nguyen; Mindy Kha; Angelina Iniguez; Qiao Zhou; Teodora Kaltcheva; Roman Levytskyy; Nancy D Ebelt; Tae Hyuk Kang; Xiwei Wu; Tom Rogers; Edwin R Manuel; Yuriy Shostak; Don J Diamond; Felix Wussow.
Afiliação
  • Flavia Chiuppesi; City of Hope
  • Marcela Salazar Werner; City of Hope
  • Heidi Contreras; City of Hope
  • Hong Vu Nguyen; City of Hope
  • Joy Martinez; City of Hope
  • Soojin Park; City of Hope
  • Jenny Nguyen; City of Hope
  • Mindy Kha; City of Hope
  • Angelina Iniguez; City of Hope
  • Qiao Zhou; City of Hope
  • Teodora Kaltcheva; City of Hope
  • Roman Levytskyy; City of Hope
  • Nancy D Ebelt; City of Hope
  • Tae Hyuk Kang; City of Hope
  • Xiwei Wu; City of Hope
  • Tom Rogers; University of California at San Diego and Scripps Research
  • Edwin R Manuel; City of Hope
  • Yuriy Shostak; City of Hope
  • Don J Diamond; City of Hope
  • Felix Wussow; City of Hope
Preprint em En | PREPRINT-BIORXIV | ID: ppbiorxiv-183236
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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.Competing Interest StatementThe authors have declared no competing interest.View Full Text
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint