T细胞受体
生物
主要组织相容性复合体
计算生物学
抗原
获得性免疫系统
T细胞
单细胞测序
剧目
细胞生物学
免疫系统
表型
遗传学
基因
物理
声学
外显子组测序
作者
Joy A. Pai,Ansuman T. Satpathy
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2021-07-19
卷期号:18 (8): 881-892
被引量:288
标识
DOI:10.1038/s41592-021-01201-8
摘要
T cells express T cell receptors (TCRs) composed of somatically recombined TCRα and TCRβ chains, which mediate recognition of major histocompatibility complex (MHC)-antigen complexes and drive the antigen-specific adaptive immune response to pathogens and cancer. The TCR repertoire in each individual is highly diverse, which allows for recognition of a wide array of foreign antigens, but also presents a challenge in analyzing this response using conventional methods. Recent studies have developed high-throughput sequencing technologies to identify TCR sequences, analyze their antigen specificities using experimental and computational tools, and pair TCRs with transcriptional and epigenetic cell state phenotypes in single cells. In this Review, we highlight these technological advances and describe how they have been applied to discover fundamental insights into T cell-mediated immunity.
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