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Protective activity of mRNA vaccines against ancestral and variant SARS-CoV-2 strains
Baoling Ying; Bradley Whitener; Laura A VanBlargan; Ahmed O Hassan; Swathi Shrihari; Chieh-Yu Liang; Courtney E Karl; Samantha Mackin; Rita E Chen; Natasha M Kafai; Samuel H Wilks; Derek J. Smith; Juan Manuel Carreno; Gagandeep Singh; Florian Krammer; Andrea Carfi; Sayda Elbashir; Darin K Edwards; Larissa B Thackray; Michael S Diamond.
Afiliación
  • Baoling Ying; Washington University
  • Bradley Whitener; Washington University
  • Laura A VanBlargan; Washington University
  • Ahmed O Hassan; Washington University
  • Swathi Shrihari; Washington University
  • Chieh-Yu Liang; Washington University
  • Courtney E Karl; Washington University
  • Samantha Mackin; Washington University
  • Rita E Chen; Washington University School of Medicine
  • Natasha M Kafai; Washington University
  • Samuel H Wilks; University of Cambridge
  • Derek J. Smith; University of Cambridge
  • Juan Manuel Carreno; Icahn School of Medicine at Mount Sinai
  • Gagandeep Singh; Icahn School of Medicine at Mount Sinai
  • Florian Krammer; Icahn School of Medicine at Mount Sinai
  • Andrea Carfi; Moderna
  • Sayda Elbashir; Moderna
  • Darin K Edwards; Moderna Inc
  • Larissa B Thackray; Washington University
  • Michael S Diamond; Washington University
Preprint en Inglés | bioRxiv | ID: ppbiorxiv-457693
ABSTRACT
Although mRNA vaccines prevent COVID-19, variants jeopardize their efficacy as immunity wanes. Here, we assessed the immunogenicity and protective activity of historical (mRNA-1273, designed for Wuhan-1 spike) or modified (mRNA-1273.351, designed for B.1.351 spike) preclinical Moderna mRNA vaccines in 129S2 and K18-hACE2 mice. Immunization with high or low dose formulations of mRNA vaccines induced neutralizing antibodies in serum against ancestral SARS-CoV-2 and several variants, although levels were lower particularly against the B.1.617.2 (Delta) virus. Protection against weight loss and lung pathology was observed with all high-dose vaccines against all viruses. Nonetheless, low-dose formulations of the vaccines, which produced lower magnitude antibody and T cell responses, and serve as a possible model for waning immunity, showed breakthrough lung infection and pneumonia with B.1.617.2. Thus, as levels of immunity induced by mRNA vaccines decline, breakthrough infection and disease likely will occur with some SARS-CoV-2 variants, suggesting a need for additional booster regimens.
Licencia
cc_by_nc_nd
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2021 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2021 Tipo del documento: Preprint
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