T细胞受体
主要组织相容性复合体
生物
抗原
T细胞
计算生物学
细胞生物学
质量细胞仪
免疫学
免疫系统
遗传学
表型
基因
作者
Alok V. Joglekar,Guideng Li
出处
期刊:Nature Methods
[Springer Nature]
日期:2020-07-06
卷期号:18 (8): 873-880
被引量:104
标识
DOI:10.1038/s41592-020-0867-z
摘要
T cells respond to threats in an antigen-specific manner using T cell receptors (TCRs) that recognize short peptide antigens presented on major histocompatibility complex (MHC) proteins. The TCR-peptide-MHC interaction mediated between a T cell and its target cell dictates its function and thereby influences its role in disease. A lack of approaches for antigen discovery has limited the fundamental understanding of the antigenic landscape of the overall T cell response. Recent advances in high-throughput sequencing, mass cytometry, microfluidics and computational biology have led to a surge in approaches to address the challenge of T cell antigen discovery. Here, we summarize the scope of this challenge, discuss in depth the recent exciting work and highlight the outstanding questions and remaining technical hurdles in this field.
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