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Virus-like particle displaying SARS-CoV-2 receptor binding domain elicits neutralizing antibodies and is protective in a challenge model

Julia L. McKechnie, Brooke Fiala, Clancey Wolf, Daniel Ellis, Douglas Holtzman, Andrew Feldhaus
doi: https://doi.org/10.1101/2022.11.29.518404
Julia L. McKechnie
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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  • For correspondence: julia.mckechnie@icosavax.com
Brooke Fiala
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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Clancey Wolf
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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Daniel Ellis
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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Douglas Holtzman
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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Andrew Feldhaus
aIcosavax, Inc., 1930 Boren Ave, Suite 1000, Seattle, WA 98101, USA
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Abstract

While the effort to vaccinate people against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has largely been successful, particularly in the developed world, the rise of new variants as well as waning immunity illustrate the need for a new generation of vaccines that provide broader and/or more durable protection against infection and severe disease. Here we describe the generation and characterization of IVX-411, a computationally designed, two-component virus-like particle (VLP) displaying the ancestral SARS-CoV-2 receptor binding domain (RBD) on its surface. Immunization of mice with IVX-411 generates neutralizing antibodies against the ancestral strain as well as three variants of concern. Neutralizing antibody titers elicited by IVX-411 are durable and significantly higher than those elicited by immunization with soluble RBD and spike antigens. Furthermore, immunization with IVX-411 is shown to be protective in a Syrian Golden hamster challenge model using two different strains of SARS-CoV-2. Overall, these studies demonstrate that IVX-411 is highly immunogenic and capable of eliciting broad, protective immunity.

Competing Interest Statement

All authors are employees and stockholders of Icosavax, Inc.

  • Abbreviations

    COVID-19
    coronavirus disease 2019
    SARS-CoV-2
    severe acute respiratory syndrome coronavirus 2
    VOCs
    variants of concern
    S
    spike protein
    RBD
    receptor binding domain
    ACE2
    angiotensin-converting enzyme 2
    VLPs
    virus-like particles
    LLPCs
    long-lived plasma cells
    IM
    intramuscular
    SEC
    size exclusion chromatography
    DLS
    dynamic light scattering
    BLI
    biolayer interferometry
    nsTEM
    negative stain transmission electron microscopy
    PNA
    pseudo-particle neutralization assay
  • Copyright 
    The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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    Posted November 29, 2022.
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    Virus-like particle displaying SARS-CoV-2 receptor binding domain elicits neutralizing antibodies and is protective in a challenge model
    Julia L. McKechnie, Brooke Fiala, Clancey Wolf, Daniel Ellis, Douglas Holtzman, Andrew Feldhaus
    bioRxiv 2022.11.29.518404; doi: https://doi.org/10.1101/2022.11.29.518404
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    Virus-like particle displaying SARS-CoV-2 receptor binding domain elicits neutralizing antibodies and is protective in a challenge model
    Julia L. McKechnie, Brooke Fiala, Clancey Wolf, Daniel Ellis, Douglas Holtzman, Andrew Feldhaus
    bioRxiv 2022.11.29.518404; doi: https://doi.org/10.1101/2022.11.29.518404

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