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Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization.
Chiba, Shiho; Frey, Steven J; Halfmann, Peter J; Kuroda, Makoto; Maemura, Tadashi; Yang, Jie E; Wright, Elizabeth R; Kawaoka, Yoshihiro; Kane, Ravi S.
  • Chiba S; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.
  • Frey SJ; School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
  • Halfmann PJ; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.
  • Kuroda M; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.
  • Maemura T; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.
  • Yang JE; Department of Biochemistry, University of Wisconsin, Madison, WI, USA.
  • Wright ER; Cryo-EM Research Center, Department of Biochemistry, University of Wisconsin, Madison, WI, USA.
  • Kawaoka Y; Department of Biochemistry, University of Wisconsin, Madison, WI, USA.
  • Kane RS; Cryo-EM Research Center, Department of Biochemistry, University of Wisconsin, Madison, WI, USA.
Commun Biol ; 4(1): 597, 2021 05 19.
Article in English | MEDLINE | ID: covidwho-1236095
ABSTRACT
The COVID-19 pandemic continues to wreak havoc as worldwide SARS-CoV-2 infection, hospitalization, and death rates climb unabated. Effective vaccines remain the most promising approach to counter SARS-CoV-2. Yet, while promising results are emerging from COVID-19 vaccine trials, the need for multiple doses and the challenges associated with the widespread distribution and administration of vaccines remain concerns. Here, we engineered the coat protein of the MS2 bacteriophage and generated nanoparticles displaying multiple copies of the SARS-CoV-2 spike (S) protein. The use of these nanoparticles as vaccines generated high neutralizing antibody titers and protected Syrian hamsters from a challenge with SARS-CoV-2 after a single immunization with no infectious virus detected in the lungs. This nanoparticle-based vaccine platform thus provides protection after a single immunization and may be broadly applicable for protecting against SARS-CoV-2 and future pathogens with pandemic potential.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pandemics / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Topics: Vaccines Limits: Animals / Female / Humans Language: English Journal: Commun Biol Year: 2021 Document Type: Article Affiliation country: S42003-021-02128-8

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pandemics / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Topics: Vaccines Limits: Animals / Female / Humans Language: English Journal: Commun Biol Year: 2021 Document Type: Article Affiliation country: S42003-021-02128-8