| Literature DB >> 31484734 |
Julian Q Zhou1, Steven H Kleinstein2,3,4.
Abstract
B cell clonal expansion is vital for adaptive immunity. High-throughput BCR sequencing enables investigating this process but requires computational inference to identify clonal relationships. This inference usually relies on only the BCR H chain, as most current protocols do not preserve H:L chain pairing. The extent to which paired L chains aids inference is unknown. Using human single-cell paired BCR datasets, we assessed the ability of H chain-based clonal clustering to identify clones. Of the expanded clones identified, <20% grouped cells expressing inconsistent L chains. H chains from these misclustered clones contained more distant junction sequences and shared fewer V segment mutations than the accurate clones. This suggests that additional H chain information could be leveraged to refine clonal relationships. Conversely, L chains were insufficient to refine H chain-based clonal clusters. Overall, the BCR H chain alone is sufficient to identify clonal relationships with confidence.Entities:
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Year: 2019 PMID: 31484734 PMCID: PMC6865802 DOI: 10.4049/jimmunol.1900666
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422