Broadly neutralizing humanized SARS-CoV-2 antibody binds to a conserved epitope on Spike and provides antiviral protection through inhalation-based delivery in non-human primates.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
08 2023
Historique:
received: 22 12 2022
accepted: 03 07 2023
medline: 4 8 2023
pubmed: 2 8 2023
entrez: 2 8 2023
Statut: epublish

Résumé

The COVID-19 pandemic represents a global challenge that has impacted and is expected to continue to impact the lives and health of people across the world for the foreseeable future. The rollout of vaccines has provided highly anticipated relief, but effective therapeutics are required to further reduce the risk and severity of infections. Monoclonal antibodies have been shown to be effective as therapeutics for SARS-CoV-2, but as new variants of concern (VoC) continue to emerge, their utility and use have waned due to limited or no efficacy against these variants. Furthermore, cumbersome systemic administration limits easy and broad access to such drugs. As well, concentrations of systemically administered antibodies in the mucosal epithelium, a primary site of initial infection, are dependent on neonatal Fc receptor mediated transport and require high drug concentrations. To reduce the viral load more effectively in the lung, we developed an inhalable formulation of a SARS-CoV-2 neutralizing antibody binding to a conserved epitope on the Spike protein, ensuring pan-neutralizing properties. Administration of this antibody via a vibrating mesh nebulization device retained antibody integrity and resulted in effective distribution of the antibody in the upper and lower respiratory tract of non-human primates (NHP). In comparison with intravenous administration, significantly higher antibody concentrations can be obtained in the lung, resulting in highly effective reduction in viral load post SARS-CoV-2 challenge. This approach may reduce the barriers of access and uptake of antibody therapeutics in real-world clinical settings and provide a more effective blueprint for targeting existing and potentially emerging respiratory tract viruses.

Identifiants

pubmed: 37531329
doi: 10.1371/journal.ppat.1011532
pii: PPATHOGENS-D-22-02220
pmc: PMC10395824
doi:

Substances chimiques

Antiviral Agents 0
Antibodies, Viral 0
Antibodies, Neutralizing 0
Epitopes 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1011532

Subventions

Organisme : CIHR
ID : PJT-159464
Pays : Canada

Informations de copyright

Copyright: © 2023 Hermet et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist. Patent: 63/318008 Title: Humanized SARS-CoV-2 antibodies Co-inventors: A. Männik, KV, CE, BD, RLG, GK, EJ, PH, MUJ, MU, ES Patent: PCT/IB2021/059363 Title: SARS-Cov-2 neutralizing antibodies Co-inventors: GK, EJ, A.Männik, AP, DK, EŽ, MU, MUJ

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Auteurs

Paule Hermet (P)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Benoît Delache (B)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Cecile Herate (C)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Esther Wolf (E)

York University; Toronto, Canada.

Gaily Kivi (G)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Erkki Juronen (E)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Karl Mumm (K)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Eva Žusinaite (E)

University of Tartu; Tartu, Estonia.

Denis Kainov (D)

NTNU; Trondheim, Norway.

Eve Sankovski (E)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Kai Virumäe (K)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Anu Planken (A)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Andres Merits (A)

University of Tartu; Tartu, Estonia.

Jessica E Besaw (JE)

Department of Biochemistry, University of Toronto; Toronto, Canada.

Ai Woon Yee (AW)

Department of Biochemistry, University of Toronto; Toronto, Canada.

Takefumi Morizumi (T)

Department of Biochemistry, University of Toronto; Toronto, Canada.

Kyumhyuk Kim (K)

Department of Biochemistry, University of Toronto; Toronto, Canada.

Anling Kuo (A)

Department of Biochemistry, University of Toronto; Toronto, Canada.

Asma Berriche (A)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Nathalie Dereuddre-Bosquet (N)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Quentin Sconosciuti (Q)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Thibaut Naninck (T)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Francis Relouzat (F)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Mariangela Cavarelli (M)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Mart Ustav (M)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Derek Wilson (D)

York University; Toronto, Canada.

Oliver P Ernst (OP)

Department of Biochemistry, University of Toronto; Toronto, Canada.
Department of Molecular Genetics, University of Toronto; Toronto, Canada.

Andres Männik (A)

Icosagen Cell Factory OÜ; Tartu, Estonia.

Roger LeGrand (R)

Université Paris-Saclay, Inserm, CEA, Center for Immunology of Viral, Auto-immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT); Fontenay-aux-Roses, France.

Mart Ustav (M)

Icosagen Cell Factory OÜ; Tartu, Estonia.

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