Vaccine-mediated protection against Merbecovirus and Sarbecovirus challenge in mice.


Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
31 10 2023
Historique:
received: 02 05 2023
revised: 30 08 2023
accepted: 26 09 2023
medline: 6 11 2023
pubmed: 20 10 2023
entrez: 20 10 2023
Statut: ppublish

Résumé

The emergence of three highly pathogenic human coronaviruses-severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003, Middle Eastern respiratory syndrome (MERS)-CoV in 2012, and SARS-CoV-2 in 2019-underlines the need to develop broadly active vaccines against the Merbecovirus and Sarbecovirus betacoronavirus subgenera. While SARS-CoV-2 vaccines protect against severe COVID-19, they do not protect against other sarbecoviruses or merbecoviruses. Here, we vaccinate mice with a trivalent sortase-conjugate nanoparticle (scNP) vaccine containing the SARS-CoV-2, RsSHC014, and MERS-CoV receptor-binding domains (RBDs), which elicited live-virus neutralizing antibody responses. The trivalent RBD scNP elicited serum neutralizing antibodies against bat zoonotic Wuhan Institute of Virology-1 (WIV-1)-CoV, SARS-CoV, SARS-CoV-2 BA.1, SARS-CoV-2 XBB.1.5, and MERS-CoV live viruses. The monovalent SARS-CoV-2 RBD scNP vaccine only protected against Sarbecovirus challenge, whereas the trivalent RBD scNP vaccine protected against both Merbecovirus and Sarbecovirus challenge in highly pathogenic and lethal mouse models. This study demonstrates proof of concept for a single pan-sarbecovirus/pan-merbecovirus vaccine that protects against three highly pathogenic human coronaviruses spanning two betacoronavirus subgenera.

Identifiants

pubmed: 37858337
pii: S2211-1247(23)01260-3
doi: 10.1016/j.celrep.2023.113248
pii:
doi:

Substances chimiques

COVID-19 Vaccines 0
Antibodies, Viral 0
Antibodies, Neutralizing 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

113248

Subventions

Organisme : NCI NIH HHS
ID : U54 CA260543
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI158571
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201700035I
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests B.F.H. and K.O.S. have filed US patents regarding the nanoparticle vaccine. R.S.B. is on the scientific advisory boards of VaxArt, Invivyd, and Takeda.

Auteurs

David R Martinez (DR)

Department of Immunobiology, Yale School of Medicine, New Haven, CT 06510, USA; Yale Center for Infection and Immunity, Yale School of Medicine, New Haven, CT 06510, USA. Electronic address: david.martinez@yale.edu.

Alexandra Schäfer (A)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Tyler D Gavitt (TD)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Michael L Mallory (ML)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Esther Lee (E)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Nicholas J Catanzaro (NJ)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Haiyan Chen (H)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Kendra Gully (K)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Trevor Scobey (T)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Pooja Korategere (P)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Alecia Brown (A)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Lena Smith (L)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Robert Parks (R)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Maggie Barr (M)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Amanda Newman (A)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Cindy Bowman (C)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

John M Powers (JM)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Erik J Soderblom (EJ)

Proteomics and Metabolomics Core Facility, Duke University School of Medicine, Durham, NC 27710, USA.

Katayoun Mansouri (K)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Robert J Edwards (RJ)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.

Ralph S Baric (RS)

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. Electronic address: rbaric@email.unc.edu.

Barton F Haynes (BF)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: barton.haynes@duke.edu.

Kevin O Saunders (KO)

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: kevin.saunders@duke.edu.

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