Leah L Weber, Derek Reiman, Mrinmoy S Roddur, Yuanyuan Qi, Mohammed El-Kebir, Aly A Khan
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引用次数: 0
Abstract
Single-cell RNA sequencing (scRNA-seq) enables comprehensive characterization of the micro-evolutionary processes of B cells during an adaptive immune response, capturing features of somatic hypermutation (SHM) and class switch recombination (CSR). Existing phylogenetic approaches for reconstructing B cell evolution have primarily focused on the SHM process alone. Here, we present tree inference of B cell clonal lineages (TRIBAL), an algorithm designed to optimally reconstruct the evolutionary history of B cell clonal lineages undergoing both SHM and CSR from scRNA-seq data. Through simulations, we demonstrate that TRIBAL produces more comprehensive and accurate B cell lineage trees compared to existing methods. Using real-world datasets, TRIBAL successfully recapitulates expected biological trends in a model affinity maturation system while reconstructing evolutionary histories with more parsimonious class switching than state-of-the-art methods. Thus, TRIBAL significantly improves B cell lineage tracing, useful for modeling vaccine responses, disease progression, and the identification of therapeutic antibodies.
单细胞 RNA 测序(scRNA-seq)能全面描述适应性免疫反应过程中 B 细胞的微进化过程,捕捉体细胞超突变(SHM)和类开关重组(CSR)的特征。现有的重建 B 细胞进化的系统发生学方法主要只关注 SHM 过程。在这里,我们介绍了B细胞克隆系的树推断(TRIBAL),这是一种旨在从scRNA-seq数据中优化重建同时经历SHM和CSR的B细胞克隆系进化史的算法。通过模拟,我们证明与现有方法相比,TRIBAL 能生成更全面、更准确的 B 细胞系树。利用真实世界的数据集,TRIBAL 成功地再现了模型亲和力成熟系统中预期的生物学趋势,同时与最先进的方法相比,TRIBAL 以更简洁的类别切换重建了进化史。因此,TRIBAL 显著改善了 B 细胞系的追踪,对疫苗反应建模、疾病进展和治疗性抗体的鉴定非常有用。