Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/172999
Title: Human soluble ACE2 improves the effect of remdesivir in SARS-CoV-2 infection
Author: Monteil, Vanessa
Dyczynski, Matheus
Lauschke, Volker M.
Kwon, Hyesoo
Wirnsberger, Gerald
Youhanna, Sonia
Zhang, Haibo
Slutsky, Arthur S.
Hurtado del Pozo, Carmen
Horn, Moritz
Montserrat, Núria
Penninger, Josef M.
Mirazimi, Ali
Keywords: SARS-CoV-2
Assaigs clínics
SARS-CoV-2
Clinical trials
Issue Date: 14-Dec-2020
Abstract: There is a critical need for safe and effective drugs for COVID-19. Only remdesivir has received authorization for COVID-19 and has been shown to improve outcomes but not decrease mortality. However, the dose of remdesivir is limited by hepatic and kidney toxicity. ACE2 is the critical cell surface receptor for SARS-CoV-2. Here, we investigated additive effect of combination therapy using remdesivir with recombinant soluble ACE2 (high/low dose) on Vero E6 and kidney organoids, targeting two different modalities of SARS-CoV-2 life cycle: cell entry via its receptor ACE2 and intracellular viral RNA replication. This combination treatment markedly improved their therapeutic windows against SARS-CoV-2 in both models. By using single amino-acid resolution screening in haploid ES cells, we report a singular critical pathway required for remdesivir toxicity, namely, Adenylate Kinase 2. The data provided here demonstrate that combining two therapeutic modalities with different targets, common strategy in HIV treatment, exhibit strong additive effects at sub-toxic concentrations. Our data lay the groundwork for the study of combinatorial regimens in future COVID-19 clinical trials.
Note: Reproducció del document publicat a: https://doi.org/10.15252/emmm.202013426
It is part of: EMBO Molecular Medicine, 2020, vol. 13, p.e13426
URI: http://hdl.handle.net/2445/172999
Related resource: https://doi.org/10.15252/emmm.202013426
Appears in Collections:Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))

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