Inhalable Nanofitin demonstrates high neutralization of SARS-CoV-2 virus via direct application in respiratory tract.

Nanofitin antibody mimetic infectious disease inhalable nebulization protein scaffold pulmonary delivery

Journal

Molecular therapy : the journal of the American Society of Gene Therapy
ISSN: 1525-0024
Titre abrégé: Mol Ther
Pays: United States
ID NLM: 100890581

Informations de publication

Date de publication:
04 10 2023
Historique:
received: 12 04 2023
revised: 04 08 2023
accepted: 10 08 2023
pmc-release: 04 10 2024
medline: 9 10 2023
pubmed: 1 9 2023
entrez: 31 8 2023
Statut: ppublish

Résumé

Nanofitins are small and hyperthermostable alternative protein scaffolds that display physicochemical properties making them suitable for the development of topical therapeutics, notably for the treatment of pulmonary infectious diseases. Local administration of biologics to the lungs involves a particularly stressful step of nebulization that is poorly tolerated by most antibodies, which limits their application by this delivery route. During the COVID-19 pandemic, we generated anti-SARS-CoV-2 monomeric Nanofitins of high specificity for the spike protein. Hit Nanofitin candidates were identified based on their binding properties with punctual spike mutants and assembled into a linear multimeric construction constituting of four different Nanofitins, allowing the generation of a highly potent anti-SARS-CoV-2 molecule. The therapeutic efficacy of the multimeric assembly was demonstrated both in in vitro and in vivo models. Interestingly, the neutralization mechanism of the multimeric construction seems to involve a particular conformation switch of the spike trimer. In addition, we reported the stability and the conserved activity of the tetrameric construction after nebulization. This advantageous developability feature for pulmonary administration associated with the ease of assembly, as well as the fast generation process position the Nanofitin technology as a potential therapeutic solution for emerging infectious diseases.

Identifiants

pubmed: 37652011
pii: S1525-0016(23)00442-2
doi: 10.1016/j.ymthe.2023.08.010
pmc: PMC10556219
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2861-2871

Informations de copyright

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

Déclaration de conflit d'intérêts

Declaration of interests The Nanofitin technology described in this study, commercialized by Affilogic, uses the patent application owned by Institut Pasteur and Center National de la Recherche Scientifique (CNRS): “OB-fold used as scaffold for engineering new specific binders”; PCT/IB2007/004388. Affilogic SAS, Nantes, France, provided support for the study and participated in study design, conducted the study, and provided data collection, management and interpretation. S.V., E.E, J.P., L.N., M.C., S.H., are employees of Affilogic SAS. O.K. is the CEO and the owner of Affilogic SAS.

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Auteurs

Sébastien Viollet (S)

Affilogic SAS, 44300 Nantes, France. Electronic address: sebastien.viollet@affilogic.com.

Elise Enouf (E)

Affilogic SAS, 44300 Nantes, France.

Justine Picot (J)

Affilogic SAS, 44300 Nantes, France.

Léna Noël (L)

Affilogic SAS, 44300 Nantes, France.

Simon Huet (S)

Affilogic SAS, 44300 Nantes, France.

Déborah Le Pennec (D)

INSERM, Research Center for Respiratory Diseases, U1100, F-37032 Tours, France; University of Tours, F-37032 Tours, France.

Thomas Sécher (T)

INSERM, Research Center for Respiratory Diseases, U1100, F-37032 Tours, France; University of Tours, F-37032 Tours, France.

Nathalie Heuzé-Vourc'h (N)

INSERM, Research Center for Respiratory Diseases, U1100, F-37032 Tours, France; University of Tours, F-37032 Tours, France.

Olivier Kitten (O)

Affilogic SAS, 44300 Nantes, France.

Mathieu Cinier (M)

Affilogic SAS, 44300 Nantes, France.

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Classifications MeSH