Discovery of a SARS-CoV-2 Broadly-Acting Neutralizing Antibody with Activity against Omicron and Omicron + R346K Variants
Duty, J. A.; Kraus, T. A.; Zhou, H.; Zhang, Y.; Shaabani, N.; Yildiz, S.; Du, N.; Singh, A.; Miorin, L.; Li, D.; Stegman, K.; Ophir, S. I.; Cao, X.; Atanasoff, K.; Lim, R.; Kowdle, S. S.; Carreno, J. M.; Rivero-Nava, L.; Raskin, A.; Moreno, E.; Johnson, S.; Rathnasinghe, R.; Pai, C. I.; Kehrer, T.; Paz Cabral, E.; Jangra, S.; Healy, L. D.; Singh, G.; Warang, P.; Simon, V.; Sordillo, M. E.; van Bakel, H.; Liu, Y.; Sun, W.; Kerwin, L.; Palese, P.; Teijaro, J.; Schotsaert, M.; Krammer, F.; Bresson, D.; Garcia-Sastre, A.; Fu, Y.; Lee, B.; Powers, C.; Moran, T. M.; Ji, H.; Tortorella, D.; Allen, R.
Show abstract
The continual emergence of SARS-CoV-2 variants of concern, in particular the newly emerged Omicron (B.1.1.529) variant, has rendered ineffective a number of previously EUA approved SARS-CoV-2 neutralizing antibody therapies. Furthermore, even those approved antibodies with neutralizing activity against Omicron are reportedly ineffective against the subset of Omicron variants that contain a R346K substitution, demonstrating the continued need for discovery and characterization of candidate therapeutic antibodies with the breadth and potency of neutralizing activity required to treat newly diagnosed COVID-19 linked to recently emerged variants of concern. Following a campaign of antibody discovery based on the vaccination of Harbour H2L2 mice with defined SARS-CoV-2 spike domains, we have characterized the activity of a large collection of Spike-binding antibodies and identified a lead neutralizing human IgG1 LALA antibody, STI-9167. STI-9167 has potent, broad-spectrum neutralizing activity against the current SARS-COV-2 variants of concern and retained activity against the Omicron and Omicron + R346K variants in both pseudotype and live virus neutralization assays. Furthermore, STI-9167 nAb administered intranasally or intravenously provided protection against weight loss and reduced virus lung titers to levels below the limit of quantitation in Omicron-infected K18-hACE2 transgenic mice. With this established activity profile, a cGMP cell line has been developed and used to produce cGMP drug product intended for use in human clinical trials.
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