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The analysis of clonal expansions in normal and autoimmune B cell repertoires
Journal article   Open access   Peer reviewed

The analysis of clonal expansions in normal and autoimmune B cell repertoires

Uri Hershberg and Eline T. Luning Prak
Philosophical transactions of the Royal Society of London. Series B. Biological sciences, v 370(1676), 20140239
05 Sep 2015
PMID: 26194753
url
https://doi.org/10.1098/rstb.2014.0239View
Published, Version of Record (VoR)CC BY V4.0 Open

Abstract

Biology Life Sciences & Biomedicine Life Sciences & Biomedicine - Other Topics Science & Technology
Clones are the fundamental building blocks of immune repertoires. The number of different clones relates to the diversity of the repertoire, whereas their size and sequence diversity are linked to selective pressures. Selective pressures act both between clones and within different sequence variants of a clone. Understanding how clonal selection shapes the immune repertoire is one of the most basic questions in all of immunology. But how are individual clones defined? Here we discuss different approaches for defining clones, starting with how antibodies are diversified during different stages of B cell development. Next, we discuss how clones are defined using different experimental methods. We focus on high-throughput sequencing datasets, and the computational challenges and opportunities that these data have for mining the antibody repertoire landscape. We discuss methods that visualize sequence variants within the same clone and allow us to consider collections of shared mutations to determine which sequences share a common ancestry. Finally, we comment on features of frequently encountered expanded B cell clones that may be of particular interest in the setting of autoimmunity and other chronic conditions.

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Domestic collaboration
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Biology
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