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SARS-CoV-2 protein subunit vaccination elicits potent neutralizing antibody responses
Marco Mandolesi; Daniel J Sheward; Leo Hanke; Junjie Ma; Pradeepa Pushparaj; Laura Perez Vidakovics; Changil Kim; Karin Loré; Xaquin Castro Dopico; Jonathan M Coquet; Gerald McInerney; Gunilla B Karlsson Hedestam; Ben Murrell.
Afiliação
  • Marco Mandolesi; Karolinska Institutet
  • Daniel J Sheward; Karolinska Institutet
  • Leo Hanke; Karolinska Institutet
  • Junjie Ma; Karolinska Institutet
  • Pradeepa Pushparaj; Karolinska Institutet
  • Laura Perez Vidakovics; Karolinska Institutet
  • Changil Kim; Karolinska Institutet
  • Karin Loré; Karolinska Institutet
  • Xaquin Castro Dopico; Karolinska Institutet
  • Jonathan M Coquet; Karolinska Institutet
  • Gerald McInerney; Karolinska Institutet
  • Gunilla B Karlsson Hedestam; Karolinska Institutet
  • Ben Murrell; Karolinska Institutet
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-228486
ABSTRACT
The outbreak and spread of SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus 2), the cause of coronavirus disease 2019 (COVID-19), is a current global health emergency and a prophylactic vaccine is needed urgently. The spike glycoprotein of SARS-CoV-2 mediates entry into host cells, and thus is a target for neutralizing antibodies and vaccine design. Here we show that adjuvanted protein immunization with SARS-CoV-2 spike trimers, stabilized in prefusion conformation 1, results in potent antibody responses in mice and rhesus macaques with neutralizing antibody titers orders of magnitude greater than those typically measured in serum from SARS-CoV-2 seropositive humans. Neutralizing antibody responses were observed after a single dose, with exceptionally high titers achieved after boosting. Furthermore, neutralizing antibody titers elicited by a dose-sparing regimen in mice were similar to those obtained from a high dose regimen. Taken together, these data strongly support the development of adjuvanted SARS-CoV-2 prefusion-stabilized spike protein subunit vaccines.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
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