Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Department of Biology, Institute of Microbiology, ETH Zurich, Zurich, Switzerland.
Front Immunol. 2018 Oct 2;9:2149. doi: 10.3389/fimmu.2018.02149. eCollection 2018.
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.
抗体进化研究传统上仅限于跟踪单个克隆谱系(源自单个 V-(D)-J 重组的 B 细胞)随时间的变化,或研究批量功能变化(例如,追踪血清多克隆抗体蛋白)。研究单个 B 细胞忽略了大部分体液免疫反应,而批量功能研究缺乏必要的分辨率来分析共存的克隆多样性。高通量测序 (HTS) 技术和生物信息学的最新进展使得有可能在单个库中检查多个共同进化的抗体单克隆谱系。为了更好地了解病原体的存在如何决定抗体库的全局进化,已经引入了大量伴随的方法和工具。在这里,我们全面总结了抗体反应系统系统发育这一新兴领域的巨大进展。我们介绍了涵盖库系统发生学史、最新工具的概述,并展望了这个快速发展和充满希望的领域的未来方向。