#dc-system-status
for updates. The development team can be contacted at datacentre@scilifelab.se
if you have any question.Ehling RA, Weber CR, Mason DM, Friedensohn S, Wagner B, Bieberich F, Kapetanovic E, Vazquez-Lombardi R, Di Roberto RB, Hong KL, Wagner C, Pataia M, Overath MD, Sheward DJ, Murrell B, Yermanos A, Cuny AP, Savic M, Rudolf F, Reddy ST
Cell Rep - (-) 110242 [2021-12-22; online 2021-12-22]
Characterization of COVID-19 antibodies has largely focused on memory B cells; however, it is the antibody-secreting plasma cells that are directly responsible for the production of serum antibodies, which play a critical role in resolving SARS-CoV-2 infection. Little is known about the specificity of plasma cells, largely because plasma cells lack surface antibody expression, thereby complicating their screening. Here, we describe a technology pipeline that integrates single-cell antibody repertoire sequencing and mammalian display to interrogate the specificity of plasma cells from 16 convalescent patients. Single-cell sequencing allows us to profile antibody repertoire features and identify expanded clonal lineages. Mammalian display screening is used to reveal that 43 antibodies (of 132 candidates) derived from expanded plasma cell lineages are specific to SARS-CoV-2 antigens, including antibodies with high affinity to the SARS-CoV-2 receptor-binding domain (RBD) that exhibit potent neutralization and broad binding to the RBD of SARS-CoV-2 variants (of concern/interest).
PubMed 34998467
DOI 10.1016/j.celrep.2021.110242
Crossref 10.1016/j.celrep.2021.110242
pii: S2211-1247(21)01751-4
https://github.com/LSSI-ETH
Fully annotated extracted antibody sequences and single cell results
http://www.ncbi.nlm.nih.gov/bioproject/782883
http://www.ncbi.nlm.nih.gov/bioproject/782992