Characterization of a Novel ACE2-Based Therapeutic with Enhanced Rather than Reduced Activity against SARS-CoV-2 Variants

Author:

Ferrari Mathieu1ORCID,Mekkaoui Leila1,Ilca F. Tudor1,Akbar Zulaikha1,Bughda Reyisa1,Lamb Katarina1,Ward Katarzyna1,Parekh Farhaan1,Karattil Rajeev1,Allen Christopher1,Wu Philip1,Baldan Vania1,Mattiuzzo Giada2,Bentley Emma M.2,Takeuchi Yasuhiro23,Sillibourne James1,Datta Preeta1,Kinna Alexander1,Pule Martin1,Onuoha Shimobi C.1

Affiliation:

1. Autolus Limited, The MediaWorks, London, United Kingdom

2. National Institute for Biological Standards and Control, Herts, United Kingdom

3. Division of Infection and Immunity, University College London, London, United Kingdom

Abstract

Mutational drift of SARS-CoV-2 risks rendering both therapeutics and vaccines less effective. Receptor decoy strategies utilizing soluble human ACE2 may overcome the risk of viral mutational escape since mutations disrupting viral interaction with the ACE2 decoy will by necessity decrease virulence, thereby preventing meaningful escape.

Funder

UK Research and Innovation

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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