TY - JOUR
T1 - An ACE2-Fc decoy produced in glycoengineered plants neutralizes ancestral and newly emerging SARS-CoV-2 variants and demonstrates therapeutic efficacy in hamsters
AU - Föderl-Höbenreich, Esther
AU - Izadi, Shiva
AU - Hofacker, Lara
AU - Kienzl, Nikolaus F.
AU - Castilho, Alexandra
AU - Strasser, Richard
AU - Tarrés-Freixas, Ferran
AU - Cantero, Guillermo
AU - Roca, Núria
AU - Pérez, Mònica
AU - Lorca-Oró, Cristina
AU - Usai, Carla
AU - Segalés Coma, Joaquim
AU - Vergara-Alert, Júlia
AU - Mach, Lukas
AU - Zatloukal, Kurt
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/4/2
Y1 - 2025/4/2
N2 - Newly 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.
AB - Newly 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.
KW - SARS-CoV-2
KW - Antiviral
KW - ACE2
KW - Plant-based expression platform
KW - Infectious diseases
KW - Respiratory tract diseases
KW - Plant biotechnology
KW - Pathogens
KW - Virology
UR - https://www.scopus.com/pages/publications/105001683818
U2 - 10.1038/s41598-025-95494-w
DO - 10.1038/s41598-025-95494-w
M3 - Article
C2 - 40175560
SN - 2045-2322
VL - 15
JO - Scientific reports
JF - Scientific reports
M1 - 11307
ER -