Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/109681
Title: A novel ACE2 decoy for both neutralization of SARS-CoV-2 variants and killing of infected cells
Author(s): Kegler, AlexandraLook up in the Integrated Authority File of the German National Library
Drewitz, Laura
Arndt, ClaudiaLook up in the Integrated Authority File of the German National Library
Daglar, Cansu
Rodrigues Loureiro, Liliana
Mitwasi, Nicola M. J.Look up in the Integrated Authority File of the German National Library
Neuber, ChristinLook up in the Integrated Authority File of the German National Library
González Soto, Karla Elizabeth
Bartsch, Tabea
Baraban, LarysaLook up in the Integrated Authority File of the German National Library
Ziehr, Holger
Heine, Markus
Nieter, Annabel
Moreira-Soto, AndresLook up in the Integrated Authority File of the German National Library
Kühne, Arne
Drexler, Jan FelixLook up in the Integrated Authority File of the German National Library
Seliger, BarbaraLook up in the Integrated Authority File of the German National Library
Laube, Markus
Máthé, Domokos
Pályi, Bernadett
Hajdrik, Polett
Forgách, László
Kis, Zoltán
Szigeti, Krisztián
Bergmann, Ralf
Feldmann, AnjaLook up in the Integrated Authority File of the German National Library
Bachmann, MichaelLook up in the Integrated Authority File of the German National Library
Issue Date: 2023
Type: Article
Language: English
Abstract: The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) led to millions of infections and deaths worldwide. As this virus evolves rapidly, there is a high need for treatment options that can win the race against new emerging variants of concern. Here, we describe a novel immunotherapeutic drug based on the SARS-CoV-2 entry receptor ACE2 and provide experimental evidence that it cannot only be used for (i) neutralization of SARS-CoV-2 in vitro and in SARS-CoV-2-infected animal models but also for (ii) clearance of virus-infected cells. For the latter purpose, we equipped the ACE2 decoy with an epitope tag. Thereby, we converted it to an adapter molecule, which we successfully applied in the modular platforms UniMAB and UniCAR for retargeting of either unmodified or universal chimeric antigen receptor-modified immune effector cells. Our results pave the way for a clinical application of this novel ACE2 decoy, which will clearly improve COVID-19 treatment.
URI: https://opendata.uni-halle.de//handle/1981185920/111636
http://dx.doi.org/10.25673/109681
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Frontiers in immunology
Publisher: Frontiers Media
Publisher Place: Lausanne
Volume: 14
Original Publication: 10.3389/fimmu.2023.1204543
Appears in Collections:Open Access Publikationen der MLU

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