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Potent neutralization of SARS-CoV-2 including variants of concern by vaccines presenting the receptor-binding domain multivalently from nanoscaffolds.
Halfmann, Peter J; Castro, Ana; Loeffler, Kathryn; Frey, Steven J; Chiba, Shiho; Kawaoka, Yoshihiro; Kane, Ravi S.
  • Halfmann PJ; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine University of Wisconsin Madison Wisconsin USA.
  • Castro A; School of Chemical and Biomolecular Engineering Georgia Institute of Technology Atlanta Georgia USA.
  • Loeffler K; School of Chemical and Biomolecular Engineering Georgia Institute of Technology Atlanta Georgia USA.
  • Frey SJ; School of Chemical and Biomolecular Engineering Georgia Institute of Technology Atlanta Georgia USA.
  • Chiba S; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine University of Wisconsin Madison Wisconsin USA.
  • Kawaoka Y; Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine University of Wisconsin Madison Wisconsin USA.
  • Kane RS; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science University of Tokyo Tokyo Japan.
Bioeng Transl Med ; 6(3): e10253, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1372699
ABSTRACT
The persistence of the global severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has brought to the forefront the need for safe and effective vaccination strategies. In particular, the emergence of several variants with greater infectivity and resistance to current vaccines has motivated the development of a vaccine that elicits a broadly neutralizing immune response against all variants. In this study, we used a nanoparticle-based vaccine platform for the multivalent display of the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein, the primary target of neutralizing antibodies. Multiple copies of RBD were conjugated to the SpyCatcher-mi3 protein nanoparticle to produce a highly immunogenic nanoparticle-based vaccine. RBD-SpyCatcher-mi3 vaccines elicited broadly cross-reactive antibodies that recognized the spike proteins of not just an early isolate of SARS-CoV-2, but also three SARS-CoV-2 variants of concern as well as SARS-CoV-1. Moreover, immunization elicited high neutralizing antibody titers against an early isolate of SARS-CoV-2 as well as four variants of concern, including the delta variant. These results reveal the potential of RBD-SpyCatcher-mi3 as a broadly protective vaccination strategy.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Vaccines / Variants Language: English Journal: Bioeng Transl Med Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Vaccines / Variants Language: English Journal: Bioeng Transl Med Year: 2021 Document Type: Article