Author:
Findlay-Wilson Stephen,Easterbrook Linda,Smith Sandra,Pope Neville,Aldridge Matthew,Humphries Gareth,Schuhmann Holger,Ngabo Didier,Rayner Emma,Otter Ashley,Coleman Thomas,Hicks Bethany,Halkerston Rachel,Apostolakis Kostis,Taylor Stephen,Fotheringham Susan,Horton Amanda,CanoCejas Irene,Wand Matthew,Tree Julia A.,Sutton Mark,Graham Victoria,Hewson Roger,Dowall Stuart
Abstract
AbstractThe development of new therapies against SARS-CoV-2 is required to extend the toolkit of intervention strategies to combat the global pandemic. In this study, hyperimmune plasma from sheep immunised with whole spike SARS-CoV-2 recombinant protein has been used to generate candidate products. In addition to purified IgG, we have refined candidate therapies by removing non-specific IgG via affinity binding along with fragmentation to eliminate the Fc region to create F(ab′)2 fragments. These preparations were evaluated for in vitro activity and demonstrated to be strongly neutralising against a range of SARS-CoV-2 strains, including Omicron B2.2. In addition, their protection against disease manifestations and viral loads were assessed using a hamster SARS-CoV-2 infection model. Results demonstrated protective effects of both IgG and F(ab′)2, with the latter requiring sequential dosing to maintain in vivo activity due to rapid clearance from the circulation.
Funder
National Institute for Health Research
UK Research and Innovate
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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