Rapid discovery of monoclonal antibodies by microfluidics-enabled FACS of single pathogen-specific antibody-secreting cells

利用微流控技术对单个病原体特异性抗体分泌细胞进行流式细胞术分选,快速发现单克隆抗体

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作者:Katrin Fischer ,Aleksei Lulla # ,Tsz Y So # ,Pehuén Pereyra-Gerber # ,Matthew I J Raybould # ,Timo N Kohler # ,Juan Carlos Yam-Puc # ,Tomasz S Kaminski ,Robert Hughes ,Gwendolyn L Pyeatt ,Florian Leiss-Maier ,Paul Brear ,Nicholas J Matheson ,Charlotte M Deane ,Marko Hyvönen ,James E D Thaventhiran ,Florian Hollfelder

Abstract

Monoclonal antibodies are increasingly used to prevent and treat viral infections and are pivotal in pandemic response efforts. Antibody-secreting cells (ASCs; plasma cells and plasmablasts) are an excellent source of high-affinity antibodies with therapeutic potential. Current methods to study antigen-specific ASCs either have low throughput, require expensive and labor-intensive screening or are technically demanding and therefore not widely accessible. Here we present a straightforward technology for the rapid discovery of monoclonal antibodies from ASCs. Our approach combines microfluidic encapsulation of single cells into an antibody capture hydrogel with antigen bait sorting by conventional flow cytometry. With our technology, we screened millions of mouse and human ASCs and obtained monoclonal antibodies against severe acute respiratory syndrome coronavirus 2 with high affinity (<1 pM) and neutralizing capacity (<100 ng ml-1) in 2 weeks with a high hit rate (>85% of characterized antibodies bound the target). By facilitating access to the underexplored ASC compartment, the approach enables efficient antibody discovery and immunological studies into the generation of protective antibodies.

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