Microfluidics-enabled fluorescence-activated cell sorting of single pathogen-specific antibody secreting cells for the rapid discovery of monoclonal antibodies

Katrin Fischer(University of Cambridge), Aleksei Lulla(University of Cambridge), Tsz Y. So(MRC Toxicology Unit), Pehuén Pereyra-Gerber(University of Cambridge), Matthew I. J. Raybould(University of Oxford), Timo N. Kohler(University of Cambridge), Tomasz S. Kamiński(University of Cambridge), Juan Carlos Yam‐Puc(MRC Toxicology Unit), Robert M. Hughes(MRC Toxicology Unit), Florian Leiß-Maier(University of Cambridge), P. Brear(University of Cambridge), Nicholas J. Matheson(NHS Blood and Transplant), Charlotte M. Deane(University of Oxford), Marko Hyvönen(University of Cambridge), James Thaventhiran(MRC Toxicology Unit), Florian Hollfelder(University of Cambridge)
bioRxiv (Cold Spring Harbor Laboratory)
January 12, 2023
Cited by 2Open Access
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Abstract

Abstract Monoclonal antibodies are increasingly used to prevent and treat viral infections, playing a pivotal role in pandemic response efforts. Antibody secreting cells (ASCs, plasma cells and plasmablasts) are an excellent source of high-affinity antibodies with therapeutic potential. Current methodologies to study antigen-specific ASCs either have low throughput, require expensive and labour-intensive screening or are technically demanding and therefore not accessible to the wider research community. Here, we present a straightforward technology for the rapid discovery of monoclonal antibodies from ASCs: we combine 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 anti-SARS-CoV-2 monoclonal antibodies with high affinity (pM) and neutralising capacity (<100 ng/mL) in two weeks with a high hit rate (>85%). By facilitating access into the underexplored ASC compartment, we enable fast and efficient antibody discovery as well as immunological studies into the generation of protective antibodies.


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