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dc.contributor.authorFöderl-Höbenreich, Esther
dc.contributor.authorIzadi, Shiva
dc.contributor.authorHofacker, Lara
dc.contributor.authorKienzl, Nikolaus F.
dc.contributor.authorCastilho, Alexandra
dc.contributor.authorStrasser, Richard
dc.contributor.authorTarrés Freixas, Ferran
dc.contributor.authorCantero Portillo, Guillermo
dc.contributor.authorRoca, Núria
dc.contributor.authorPérez Maíllo, Mónica
dc.contributor.authorLorca-Oró, Cristina
dc.contributor.authorUsai, Carla
dc.contributor.authorSegalés, Joaquim
dc.contributor.authorVergara-Alert, Júlia
dc.contributor.authorMach, Lukas
dc.contributor.authorZatloukal, Kurt
dc.contributor.otherProducció Animalca
dc.date.accessioned2025-06-16T14:40:41Z
dc.date.available2025-06-16T14:40:41Z
dc.date.issued2025-04-02
dc.identifier.citationFöderl-Höbenreich, Esther, Shiva Izadi, Lara Hofacker, Nikolaus F Kienzl, Alexandra Castilho, Richard Strasser, Ferran Tarrés-Freixas, et al. 2025. “An ACE2-Fc Decoy Produced in Glycoengineered Plants Neutralizes Ancestral and Newly Emerging SARS-CoV-2 Variants and Demonstrates Therapeutic Efficacy in Hamsters.” Scientific Reports 15 (1). https://doi.org/10.1038/s41598-025-95494-w.ca
dc.identifier.issn2045-2322ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/4599
dc.description.abstractNewly emerging SARS-CoV-2 variants of concern (VOCs) continue to drive COVID-19 waves and are typically associated with immune escape and increased resistance to current therapeutics including monoclonal antibodies. By contrast, VOCs still display strong binding to the host cell receptor ACE2. Consistent with these properties, we have now found that a soluble ACE2-Fc decoy produced in glycoengineered plants effectively neutralizes different SARS-CoV-2 isolates and exhibits even increased potency against VOCs as compared to an ancestral virus strain. In a golden Syrian hamster model, therapeutic intranasal delivery of ACE2-Fc effectively reduced weight loss and SARS-CoV-2 replication in the lungs when administered 24 h post-inoculation. This protective effect was not observed upon treatment of the infected animals with a non-binding ACE2-Fc mutant, demonstrating that the plant-derived ACE2-Fc decoy interferes specifically with the attachment of the virus to host cells. The results obtained provide support for further development of decoy-based antiviral approaches by plant molecular pharming.ca
dc.description.sponsorshipWe thank Ulrike Vavra, Katharina Wolf and David Niedermayer for assistance with ACE2-Fc purification and characterization and Vinny Kunnummel for plant propagation and maintenance. We are grateful to Florian Krammer for his advice on the design of the in vivo study. This work was supported by funds from BOKU University and a Transnational Access Grant provided by ISIDORe (funded by the European Union’s Horizon Europe research and innovation program under grant agreement No. 101046133) to Zatloukal Innovations GmbH. This research was funded in part by the Austrian Science Fund (FWF) [W 1224/Grant https://doi.org/10.55776/W1224; P 31920/Grant https://doi.org/10.55776/P31920; P 35292/Grant https://doi.org/10.55776/P35292]. For open access purposes, the authors have applied a CC BY public copyright license to any accepted manuscript version arising from this submission. The SARS-CoV-2 variant hCoV-19/France/GE1973/2020, clade G, D614G (S) was supplied through the European Virus Archive goes Global (EVAg) platform, a project that has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No. 653316.ca
dc.format.extent13ca
dc.language.isoengca
dc.publisherNature Researchca
dc.relation.ispartofScientific Reportsca
dc.rightsAttribution 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleAn ACE2-Fc decoy produced in glycoengineered plants neutralizes ancestral and newly emerging SARS-CoV-2 variants and demonstrates therapeutic efficacy in hamstersca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDEC/HE/101046133/EU/ Integrated Services for Infectious Disease Outbreak Research/ISIDOReca
dc.relation.projectIDEC/H2020/653316/EU/European Virus Archive goes global/EVAgca
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.1038/s41598-025-95494-wca
dc.contributor.groupSanitat Animalca


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