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Nucleocapsid-specific humoral responses improve the control of SARS-CoV-2
Tanushree Dangi; Sarah Sanchez; Mincheol Park; Jacob Class; Michelle C Richner; Justin M Richner; Pablo Penaloza-MacMaster.
Afiliación
  • Tanushree Dangi; Northwestern University
  • Sarah Sanchez; Northwestern University
  • Mincheol Park; Northwestern University
  • Jacob Class; University of Illinois at Chicago
  • Michelle C Richner; University of Illinois at Chicago
  • Justin M Richner; University of Illinois at Chicago
  • Pablo Penaloza-MacMaster; Northwestern University
Preprint en Inglés | bioRxiv | ID: ppbiorxiv-483635
ABSTRACT
The spike protein of SARS-CoV-2 is a critical antigen present in all approved SARS-CoV-2 vaccines. This surface viral protein is also the target for all monoclonal antibody therapies, but it is unclear whether antibodies targeting other viral proteins can also improve protection against COVID-19. Here, we interrogate whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine, and then transferred sera from these mice into naive mice. On the next day, the recipient mice were challenged intranasally with SARS-CoV-2 to evaluate whether nucleocapsid-specific humoral responses affect viral control. Interestingly, mice that received nucleocapsid-specific sera exhibited enhanced control of a SARS-CoV-2 infection. These findings provide the first demonstration that humoral responses specific to an internal coronavirus protein can help clear infection, warranting the inclusion of other viral antigens in next-generation SARS-CoV-2 vaccines and providing a rationale for the clinical evaluation of nucleocapsid-specific monoclonals to treat COVID-19. HighlightsA SARS-CoV-2 nucleocapsid vaccine elicits robust nucleocapsid-specific antibody responses. This nucleocapsid vaccine generates memory B cells (MBC). Nucleocapsid-specific humoral responses do not prevent SARS-CoV-2 infection. Nucleocapsid-specific humoral responses help control a SARS-CoV-2 infection.
Licencia
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Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Tipo de estudio: Experimental_studies / Estudio pronóstico Idioma: Inglés Año: 2022 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Tipo de estudio: Experimental_studies / Estudio pronóstico Idioma: Inglés Año: 2022 Tipo del documento: Preprint
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