Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases

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Abstract

Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR™ (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5-4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known. © 2008 The Author(s).

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Rogers, J., Schoepp, R. J., Schröder, O., Clements, T. L., Holland, T. F., Li, J. Q., … Tozer, E. C. (2008). Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases. Protein Engineering, Design and Selection, 21(8), 495–505. https://doi.org/10.1093/protein/gzn027

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