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A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability
Emily A. Voigt; Alana Gerhardt; Derek Hanson; Peter Battisti; Sierra Reed; Jasneet Singh; Raodoh Mohamath; Madeleine F. Jennewein; Julie Bakken; Samuel Beaver; Christopher Press; Patrick Soon-Shiong; Christopher J. Paddon; Christopher B. Fox; Corey Casper.
Afiliación
  • Emily A. Voigt; Access to Advanced Health Institute, Seattle, WA
  • Alana Gerhardt; Access to Advanced Health Institute, Seattle, WA
  • Derek Hanson; Access to Advanced Health Institute, Seattle, WA
  • Peter Battisti; Access to Advanced Health Institute, Seattle, WA
  • Sierra Reed; Access to Advanced Health Institute, Seattle, WA
  • Jasneet Singh; Access to Advanced Health Institute, Seattle, WA
  • Raodoh Mohamath; Access to Advanced Health Institute, Seattle, WA
  • Madeleine F. Jennewein; Access to Advanced Health Institute, Seattle, WA
  • Julie Bakken; Access to Advanced Health Institute, Seattle, WA
  • Samuel Beaver; Access to Advanced Health Institute, Seattle, WA
  • Christopher Press; Access to Advanced Health Institute, Seattle, WA
  • Patrick Soon-Shiong; ImmunityBio, Inc., Culver City, CA
  • Christopher J. Paddon; Amyris, Inc., Emeryville, CA
  • Christopher B. Fox; Access to Advanced Health Institute, Seattle, WA
  • Corey Casper; Access to Advanced Health Institute, Seattle, WA
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-485230
ABSTRACT
mRNA vaccines were the first to be authorized for use against SARS-CoV-2 and have since demonstrated high efficacy against serious illness and death. However, limitations in these vaccines have been recognized due to their requirement for cold storage, short durability of protection, and lack of access in low-resource regions. We have developed an easily-manufactured, potent self-amplifying RNA (saRNA) vaccine against SARS-CoV-2 that is stable at room temperature. This saRNA vaccine is formulated with a nanostructured lipid carrier (NLC), providing enhanced stability, improved manufacturability, and protection against degradation. In preclinical studies, this saRNA/NLC vaccine induced strong humoral immunity, as demonstrated by high pseudovirus neutralization titers to the Alpha, Beta, and Delta variants of concern and induction of long-lived bone marrow-resident antibody secreting cells. Robust Th1-biased T-cell responses were also observed after prime or homologous prime-boost in mice. Notably, the saRNA/NLC platform demonstrated thermostability at room temperature for at least 6 months when lyophilized. Taken together, this saRNA delivered by NLC represents a potential improvement in RNA technology that could allow wider access to RNA vaccines for the current COVID-19 and future pandemics.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Idioma: En Año: 2022 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Idioma: En Año: 2022 Tipo del documento: Preprint