Disease associated human TCR characterization by deep-learning framework TCR-DeepInsight
Ziwei XueiD, Lize WuiD, Bing Xin GaoiD, Ruonan TianiD, Yiru CheniD, Yicheng QiiD, Tianze Dong, Yadan Bai, Yu Shan ZhaoiD, Bing HeiD, Lie WangiD, Zuozhu LiuiD, Jianhua YaoiD, Linrong LuiD, Wanlu LiuiD
Abstract
T cell function is defined by both T cell receptors (TCR) and T cell gene expression (GEX). Although single-cell technology enables the simultaneous capture of TCR and GEX information, the lack of a reference atlas and computational tools hinders our ability to uncover the fundamental TCR usage rules and to efficiently characterize disease-associated TCRs (dTCR). Here, through the collection of million-scale single-cell GEX-TCR reference atlas comprising 20 diverse disease conditions, we revealed the intrinsic features of TCR-MHC (Major Histocompatibility Complex) restriction in CD4/CD8 lineages. We observed the higher coherence for TCR/{beta} chains in memory T cells, and detected widely-existing public TCR/{beta} pairs across individuals. Building upon the reference atlas, we introduced TCR- DeepInsight, a deep-learning framework featuring a disease specificity scoring system that enables the characterization of dTCR clusters with similar GEX-TCR. Our study provides a valuable tool for researchers to analyze single-cell GEX-TCR data and identify dTCRs comprehensively and robustly.
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