Tracing Antibody Repertoire Evolution by Systems Phylogeny

Antibody evolution studies have been traditionally limited to either tracing a single clonal lineage (B cells derived from a single V-(D)-J recombination) over time or examining bulk functionality changes (e.g., tracing serum polyclonal antibody proteins). Studying a single B cell disregards the maj...

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Main Authors: Alexander Dimitri Yermanos, Andreas Kevin Dounas, Tanja Stadler, Annette Oxenius, Sai T. Reddy
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.02149/full
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spelling doaj-54b5861b06f643269f81c5d0b49e0bd82020-11-24T23:55:59ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-10-01910.3389/fimmu.2018.02149399459Tracing Antibody Repertoire Evolution by Systems PhylogenyAlexander Dimitri Yermanos0Alexander Dimitri Yermanos1Andreas Kevin Dounas2Tanja Stadler3Annette Oxenius4Sai T. Reddy5Department of Biosystems Science and Engineering, ETH Zurich, Basel, SwitzerlandDepartment of Biology, Institute of Microbiology, ETH Zurich, Zurich, SwitzerlandDepartment of Chemistry and Applied Biosciences, ETH Zurich, Zurich, SwitzerlandDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, SwitzerlandDepartment of Biology, Institute of Microbiology, ETH Zurich, Zurich, SwitzerlandDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, SwitzerlandAntibody evolution studies have been traditionally limited to either tracing a single clonal lineage (B cells derived from a single V-(D)-J recombination) over time or examining bulk functionality changes (e.g., tracing serum polyclonal antibody proteins). Studying a single B cell disregards the majority of the humoral immune response, whereas bulk functional studies lack the necessary resolution to analyze the co-existing clonal diversity. Recent advances in high-throughput sequencing (HTS) technologies and bioinformatics have made it possible to examine multiple co-evolving antibody monoclonal lineages within the context of a single repertoire. A plethora of accompanying methods and tools have been introduced in hopes of better understanding how pathogen presence dictates the global evolution of the antibody repertoire. Here, we provide a comprehensive summary of the tremendous progress of this newly emerging field of systems phylogeny of antibody responses. We present an overview encompassing the historical developments of repertoire phylogenetics, state-of-the-art tools, and an outlook on the future directions of this fast-advancing and promising field.https://www.frontiersin.org/article/10.3389/fimmu.2018.02149/fullsystems immunologyphylogeneticsantibody lineageB cell evolutionIg-Seq
collection DOAJ
language English
format Article
sources DOAJ
author Alexander Dimitri Yermanos
Alexander Dimitri Yermanos
Andreas Kevin Dounas
Tanja Stadler
Annette Oxenius
Sai T. Reddy
spellingShingle Alexander Dimitri Yermanos
Alexander Dimitri Yermanos
Andreas Kevin Dounas
Tanja Stadler
Annette Oxenius
Sai T. Reddy
Tracing Antibody Repertoire Evolution by Systems Phylogeny
Frontiers in Immunology
systems immunology
phylogenetics
antibody lineage
B cell evolution
Ig-Seq
author_facet Alexander Dimitri Yermanos
Alexander Dimitri Yermanos
Andreas Kevin Dounas
Tanja Stadler
Annette Oxenius
Sai T. Reddy
author_sort Alexander Dimitri Yermanos
title Tracing Antibody Repertoire Evolution by Systems Phylogeny
title_short Tracing Antibody Repertoire Evolution by Systems Phylogeny
title_full Tracing Antibody Repertoire Evolution by Systems Phylogeny
title_fullStr Tracing Antibody Repertoire Evolution by Systems Phylogeny
title_full_unstemmed Tracing Antibody Repertoire Evolution by Systems Phylogeny
title_sort tracing antibody repertoire evolution by systems phylogeny
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-10-01
description Antibody evolution studies have been traditionally limited to either tracing a single clonal lineage (B cells derived from a single V-(D)-J recombination) over time or examining bulk functionality changes (e.g., tracing serum polyclonal antibody proteins). Studying a single B cell disregards the majority of the humoral immune response, whereas bulk functional studies lack the necessary resolution to analyze the co-existing clonal diversity. Recent advances in high-throughput sequencing (HTS) technologies and bioinformatics have made it possible to examine multiple co-evolving antibody monoclonal lineages within the context of a single repertoire. A plethora of accompanying methods and tools have been introduced in hopes of better understanding how pathogen presence dictates the global evolution of the antibody repertoire. Here, we provide a comprehensive summary of the tremendous progress of this newly emerging field of systems phylogeny of antibody responses. We present an overview encompassing the historical developments of repertoire phylogenetics, state-of-the-art tools, and an outlook on the future directions of this fast-advancing and promising field.
topic systems immunology
phylogenetics
antibody lineage
B cell evolution
Ig-Seq
url https://www.frontiersin.org/article/10.3389/fimmu.2018.02149/full
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