Phylogenetic analysis of migration, differentiation, and class switching in B cells

B cells undergo rapid mutation and selection for antibody binding affinity when producing antibodies capable of neutralizing pathogens. This evolutionary process can be intermixed with migration between tissues, differentiation between cellular subsets, and switching between functional isotypes. B c...

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Published inPLoS computational biology Vol. 18; no. 4; p. e1009885
Main Authors Hoehn, Kenneth B., Pybus, Oliver G., Kleinstein, Steven H.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.04.2022
Public Library of Science (PLoS)
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Summary:B cells undergo rapid mutation and selection for antibody binding affinity when producing antibodies capable of neutralizing pathogens. This evolutionary process can be intermixed with migration between tissues, differentiation between cellular subsets, and switching between functional isotypes. B cell receptor (BCR) sequence data has the potential to elucidate important information about these processes. However, there is currently no robust, generalizable framework for making such inferences from BCR sequence data. To address this, we develop three parsimony-based summary statistics to characterize migration, differentiation, and isotype switching along B cell phylogenetic trees. We use simulations to demonstrate the effectiveness of this approach. We then use this framework to infer patterns of cellular differentiation and isotype switching from high throughput BCR sequence datasets obtained from patients in a study of HIV infection and a study of food allergy. These methods are implemented in the R package dowser , available at https://dowser.readthedocs.io .
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I have read the journal’s policy and the authors of this manuscript have the following competing interests: S.H.K. receives consulting fees from Northrop Grumman and Peraton. K.B.H receives consulting fees from Prellis Biologics.
ISSN:1553-7358
1553-734X
1553-7358
DOI:10.1371/journal.pcbi.1009885