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检测全 T 细胞受体序列库中富集的 T 细胞表位特异性。

Detection of Enriched T Cell Epitope Specificity in Full T Cell Receptor Sequence Repertoires.

机构信息

Adrem Data Lab, Department of Mathematics and Computer Science, University of Antwerp, Antwerp, Belgium.

Antwerp Unit for Data Analysis and Computation in Immunology and Sequencing (AUDACIS), University of Antwerp, Antwerp, Belgium.

出版信息

Front Immunol. 2019 Nov 29;10:2820. doi: 10.3389/fimmu.2019.02820. eCollection 2019.

Abstract

High-throughput T cell receptor (TCR) sequencing allows the characterization of an individual's TCR repertoire and directly queries their immune state. However, it remains a non-trivial task to couple these sequenced TCRs to their antigenic targets. In this paper, we present a novel strategy to annotate full TCR sequence repertoires with their epitope specificities. The strategy is based on a machine learning algorithm to learn the TCR patterns common to the recognition of a specific epitope. These results are then combined with a statistical analysis to evaluate the occurrence of specific epitope-reactive TCR sequences per epitope in repertoire data. In this manner, we can directly study the capacity of full TCR repertoires to target specific epitopes of the relevant vaccines or pathogens. We demonstrate the usability of this approach on three independent datasets related to vaccine monitoring and infectious disease diagnostics by independently identifying the epitopes that are targeted by the TCR repertoire. The developed method is freely available as a web tool for academic use at tcrex.biodatamining.be.

摘要

高通量 T 细胞受体 (TCR) 测序可以描述个体的 TCR 库,并直接检测其免疫状态。然而,将这些测序的 TCR 与它们的抗原靶标联系起来仍然是一项艰巨的任务。在本文中,我们提出了一种新的策略,用其表位特异性对完整的 TCR 序列库进行注释。该策略基于机器学习算法,用于学习识别特定表位的 TCR 模式。然后,将这些结果与统计分析相结合,以评估每个表位在库数据中出现的特定表位反应性 TCR 序列。通过这种方式,我们可以直接研究完整的 TCR 库针对相关疫苗或病原体的特定表位的能力。我们通过独立识别 TCR 库靶向的表位,在三个与疫苗监测和传染病诊断相关的独立数据集上展示了该方法的可用性。所开发的方法可作为学术用途的免费网络工具在 tcrex.biodatamining.be 上使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6959/6896208/0a35946af838/fimmu-10-02820-g0001.jpg

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