Filamentous Fungus-Produced Human Monoclonal Antibody Provides SARS-CoV-2 Protection in Hamster and Non-Human Primate Models

Author:

Kaiser Franziska1,Hernandez Mariana Gonzalez1,Krüger Nadine2,Englund Ellinor3,Du Wenjuan4,Mykytyn Anna5ORCID,Raadsen Mathijs6,Lamers Mart6,Ianiski Francine Rodrigues7ORCID,Shamorkina Tatiana7ORCID,Snijder Joost7,Armando Federico8,Beythien Georg8,Ciurkiewicz Malgorzata8,Schreiner Tom9,Gruber-Dujardin Eva Eva2,Bleyer Martina2,Batura Olga2,Erffmeier Lena2,Hinkel Rabea2,Rocha Cheila2,Mirolo Monica1,Drabek Dubravka10ORCID,Bosch Berend-Jan4ORCID,Emalfarb Mark11ORCID,Valbuena Noelia11,Tchele Ronen11,Baumgärtner Wolfgang8,Saloheimo Markku12,Pöhlmann Stefan2ORCID,Grosveld Frank13,Haagmans Bart14ORCID,Osterhaus Albert15

Affiliation:

1. Research Center for Emerging Infections and Zoonosis, University of Veterinary Medicine, Foundation

2. German Primate Center - Leibniz Institute for Primate Research

3. VTT Technical Research Centre of Finland Ltd

4. Utrecht University

5. Erasmus Medical Center

6. Department of Viroscience, Erasmus Medical Center

7. Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute of Pharmaceutical Sciences

8. Department of Pathology, University of Veterinary Medicine, Foundation

9. Department of Pathology, University of Veterinary Medicine

10. Harbour BioMed,

11. Dyadic International, Inc.

12. VTT Technical Research Centre of Finland Ltd.

13. Erasmus MC

14. Erasmus University Medical Center

15. University of Veterinary Medicine Hannover, Foundation

Abstract

Abstract Monoclonal antibodies are an increasingly important tool for prophylaxis and treatment of acute virus infections like those with SARS-CoV-2. However, their use is largely limited by the length of development, yield and high production costs, as well as the need for continuous adaptation to newly emerging virus variants. Here we have used the filamentous fungus expression system Thermothelomyces heterothallica(C1), which has a natural high biosynthesis capacity for secretory enzymes and other proteins further enhanced by genetic engineering of the wild-type fungus, to produce a human monoclonal IgG1 antibody (HuMab 87G7) that neutralises SARS-CoV-2 variants of concern (VOCs) Alpha, Beta, Gamma, Delta, and Omicron. Like its mammalian cell produced equivalent, C1 produced HuMab 87G7 broadly neutralised SARS-CoV-2 VOCs in vitro and it also provided protection against Omicron and Delta VOCs in both hamsters and non-human primates, respectively. The only notable difference between the two versions was their N-linked glycosylation patterns detected by glyoproteomic analysis. Taken together, these findings demonstrate potential of the C1 expression system as a promising technology platform for the development of HuMabs in preventive and therapeutic medicine.

Publisher

Research Square Platform LLC

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