Filamentous fungus-produced human monoclonal antibody provides protection against SARS-CoV-2 in hamster and non-human primate models

Author:

Kaiser Franziska K.ORCID,Hernandez Mariana GonzalezORCID,Krüger NadineORCID,Englund Ellinor,Du Wenjuan,Mykytyn Anna Z.ORCID,Raadsen Mathijs P.ORCID,Lamers Mart M.,Rodrigues Ianiski FrancineORCID,Shamorkina Tatiana M.ORCID,Snijder JoostORCID,Armando FedericoORCID,Beythien GeorgORCID,Ciurkiewicz MalgorzataORCID,Schreiner TomORCID,Gruber-Dujardin Eva,Bleyer Martina,Batura Olga,Erffmeier Lena,Hinkel RabeaORCID,Rocha Cheila,Mirolo Monica,Drabek DubravkaORCID,Bosch Berend-JanORCID,Emalfarb MarkORCID,Valbuena Noelia,Tchelet Ronen,Baumgärtner WolfgangORCID,Saloheimo Markku,Pöhlmann StefanORCID,Grosveld FrankORCID,Haagmans Bart L.ORCID,Osterhaus Albert D.M.E.ORCID

Abstract

AbstractMonoclonal antibodies are an increasingly important tool for prophylaxis and treatment of acute virus infections like SARS-CoV-2 infection. However, their use is often restricted due to the time required for development, variable yields and high production costs, as well as the need for adaptation to newly emerging virus variants. Here we use the genetically modified filamentous fungus expression system Thermothelomyces heterothallica (C1), which has a naturally high biosynthesis capacity for secretory enzymes and other proteins, to produce a human monoclonal IgG1 antibody (HuMab 87G7) that neutralises the SARS-CoV-2 variants of concern (VOCs) Alpha, Beta, Gamma, Delta, and Omicron. Both the mammalian cell and C1 produced HuMab 87G7 broadly neutralise SARS-CoV-2 VOCs in vitro and also provide protection against VOC Omicron in hamsters. The C1 produced HuMab 87G7 is also able to protect against the Delta VOC in non-human primates. In summary, these findings show that the C1 expression system is a promising technology platform for the development of HuMabs in preventive and therapeutic medicine.

Funder

EC | Horizon 2020 Framework Programme

Publisher

Springer Science and Business Media LLC

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