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Novel ACE2 nanoparticles universally block SARS-CoV-2 variants in the human respiratory tract

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Sauvanet, Cécile | Lemos, Moara | Bezault, Armel | de Francisco, Borja Rodríguez | Chan, Michael Cw | Hui, Kenrie Py | Ng, Ka-Chun | Nicholls, John | Volkmann, Niels | Hanein, Dorit

Edité par CCSD -

International audience. Abstract The continual evolution of SARS-CoV-2 has challenged the efficacy of many COVID19 vaccines and treatment options. One strategy that evades viral escape is using the entry receptor, human Angiotensin-Converting Enzyme 2 (hACE2). Soluble hACE2 receptor domains show potential as decoys but genetic modifications are necessary to provide sufficient efficacy. However, these engineered constructs are potentially susceptible to viral escape. We combined native hACE2 with viral vectors to form nanoparticles presenting hACE2 analogous to human cells. Cell-based viral infection assays and cryogenic in-situ tomography show that hACE2 nanoparticles sequester viruses through aggregation, efficiently blocking entry of SARS-CoV-2 and its variants in model cell systems and human respiratory tract explants using native hACE2. Thus, we show that hACE2 nanoparticles have high potential as pan-variant COVID19 therapeutics.

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