bioRxiv · 10.1101/2023.05.23.541927
Full-length single-cell BCR sequencing paired with RNA sequencing reveals convergent responses to vaccination
Abstract
Single-cell RNA sequencing can to resolve transcriptional features from large numbers of individual immune cells, but techniques capable of resolving the variable regions of B cell receptors (BCR) - defining features that confer antigen specificity to B cells - remain limited, especially from widely-used 3'-barcoded libraries. Here, we report a method that for recovering paired, full-length variable region sequences of the BCRs from 3'-barcoded single-cell whole transcriptome libraries. We first verified this method could produce accurate, full-length BCR sequences. We then applied this method to profile antigen-specific B cell responses elicited against the capsular polysaccharide of Streptococcus pneumoniae serotype 3 (ST3) by glycoconjugate vaccines in infant rhesus macaques. Using our method, we defined features of the BCR associated with specificity for the ST3 antigen and showed that these sequence characteristics are present in multiple vaccinated monkeys, indicating a convergent response to vaccination. These results demonstrate the utility of our method to resolve key features of the B cell repertoire and for profiling antigen-specific responses elicited by vaccination.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Morgan, D. M., Zhang, Y., Kim, J.-H., Murillo, M., Singh, S., Loschko, J., Surendran, N., Patil, S. U., Kanevsky, I., Chorro, L., Love, J. C.. 2023-05-24. Full-length single-cell BCR sequencing paired with RNA sequencing reveals convergent responses to vaccination. https://doi.org/10.1101/2023.05.23.541927
Cite the original work for its findings. Save a collection to share your selection of sources.