Suppr超能文献

TCR 测序在癌症和自身免疫中的应用:条形码及其他。

TCR-sequencing in cancer and autoimmunity: barcodes and beyond.

机构信息

Department of Immunology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA; Evergrande Center for Immunological Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA, USA.

Center for Data Sciences, Brigham and Women's Hospital, Boston, MA, USA; Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.

出版信息

Trends Immunol. 2022 Mar;43(3):180-194. doi: 10.1016/j.it.2022.01.002. Epub 2022 Jan 25.

Abstract

The T cell receptor (TCR) endows T cells with antigen specificity and is central to nearly all aspects of T cell function. Each naïve T cell has a unique TCR sequence that is stably maintained during cell division. In this way, the TCR serves as a molecular barcode that tracks processes such as migration, differentiation, and proliferation of T cells. Recent technological advances have enabled sequencing of the TCR from single cells alongside deep molecular phenotypes on an unprecedented scale. In this review, we discuss strengths and limitations of TCR sequences as molecular barcodes and their application to study immune responses following Programmed Death-1 (PD-1) blockade in cancer. Additionally, we consider applications of TCR data beyond use as a barcode.

摘要

T 细胞受体 (TCR) 赋予 T 细胞抗原特异性,是 T 细胞几乎所有功能方面的核心。每个初始 T 细胞都有一个独特的 TCR 序列,在细胞分裂过程中稳定维持。这样,TCR 就像一个分子条码,跟踪 T 细胞的迁移、分化和增殖等过程。最近的技术进步使得能够在前所未有的规模上对单个细胞的 TCR 进行测序,同时对其进行深度分子表型分析。在这篇综述中,我们讨论了 TCR 序列作为分子条码的优缺点及其在研究癌症中程序性死亡受体-1 (PD-1) 阻断后免疫反应中的应用。此外,我们还考虑了 TCR 数据的应用,不仅限于作为条码。

相似文献

1
TCR-sequencing in cancer and autoimmunity: barcodes and beyond.
Trends Immunol. 2022 Mar;43(3):180-194. doi: 10.1016/j.it.2022.01.002. Epub 2022 Jan 25.
2
Single-Cell TCR and Transcriptome Analysis: An Indispensable Tool for Studying T-Cell Biology and Cancer Immunotherapy.
Front Immunol. 2021 Jun 7;12:689091. doi: 10.3389/fimmu.2021.689091. eCollection 2021.
3
T-Cell Receptor Repertoire Sequencing in the Era of Cancer Immunotherapy.
Clin Cancer Res. 2023 Mar 14;29(6):994-1008. doi: 10.1158/1078-0432.CCR-22-2469.
5
Analysis of TCR β CDR3 sequencing data for tracking anti-tumor immunity.
Methods Enzymol. 2019;629:443-464. doi: 10.1016/bs.mie.2019.08.006. Epub 2019 Sep 5.
6
Profiling tissue-resident T cell repertoires by RNA sequencing.
Genome Med. 2015 Nov 30;7:125. doi: 10.1186/s13073-015-0248-x.
7
Investigation of Antigen-Specific T-Cell Receptor Clusters in Human Cancers.
Clin Cancer Res. 2020 Mar 15;26(6):1359-1371. doi: 10.1158/1078-0432.CCR-19-3249. Epub 2019 Dec 12.
9
Tetramer-Associated T Cell Receptor Sequencing.
Methods Mol Biol. 2022;2574:183-208. doi: 10.1007/978-1-0716-2712-9_8.
10
Application of T cell receptor (TCR) repertoire analysis for the advancement of cancer immunotherapy.
Curr Opin Immunol. 2022 Feb;74:1-8. doi: 10.1016/j.coi.2021.07.006. Epub 2021 Aug 25.

引用本文的文献

2
THE BIOLOGY BEHIND PD-1 CHECKPOINT BLOCKADE.
Trans Am Clin Climatol Assoc. 2025;135:169-183.
3
PD-1 regulates tumor-infiltrating CD8+ T cells in both a cell-intrinsic and a cell-extrinsic fashion.
J Exp Med. 2025 Oct 6;222(10). doi: 10.1084/jem.20230542. Epub 2025 Jul 24.
4
Granzyme K CD8 T cells slow tauopathy progression by targeting microglia.
Nat Immunol. 2025 Jun 24. doi: 10.1038/s41590-025-02198-4.
5
Single-cell meta-analysis of T cells reveals clonal dynamics of response to checkpoint immunotherapy.
Cell Genom. 2025 May 14;5(5):100842. doi: 10.1016/j.xgen.2025.100842. Epub 2025 Apr 4.
9
The T cell receptor sequence influences the likelihood of T cell memory formation.
Cell Rep. 2025 Jan 28;44(1):115098. doi: 10.1016/j.celrep.2024.115098. Epub 2024 Dec 27.
10
TCellR2Vec: efficient feature selection for TCR sequences for cancer classification.
PeerJ Comput Sci. 2024 Nov 4;10:e2239. doi: 10.7717/peerj-cs.2239. eCollection 2024.

本文引用的文献

1
Deep learning-based prediction of the T cell receptor-antigen binding specificity.
Nat Mach Intell. 2021 Oct;3(10):864-875. doi: 10.1038/s42256-021-00383-2. Epub 2021 Sep 23.
2
HLA autoimmune risk alleles restrict the hypervariable region of T cell receptors.
Nat Genet. 2022 Apr;54(4):393-402. doi: 10.1038/s41588-022-01032-z. Epub 2022 Mar 24.
3
Repertoire analyses reveal T cell antigen receptor sequence features that influence T cell fate.
Nat Immunol. 2022 Mar;23(3):446-457. doi: 10.1038/s41590-022-01129-x. Epub 2022 Feb 17.
5
Pan-cancer single-cell landscape of tumor-infiltrating T cells.
Science. 2021 Dec 17;374(6574):abe6474. doi: 10.1126/science.abe6474.
6
Stem-like intestinal Th17 cells give rise to pathogenic effector T cells during autoimmunity.
Cell. 2021 Dec 22;184(26):6281-6298.e23. doi: 10.1016/j.cell.2021.11.018. Epub 2021 Dec 6.
7
High-throughput and high-dimensional single-cell analysis of antigen-specific CD8 T cells.
Nat Immunol. 2021 Dec;22(12):1590-1598. doi: 10.1038/s41590-021-01073-2. Epub 2021 Nov 22.
8
Sensitive identification of neoantigens and cognate TCRs in human solid tumors.
Nat Biotechnol. 2022 May;40(5):656-660. doi: 10.1038/s41587-021-01072-6. Epub 2021 Nov 15.
9
Arthritis flares mediated by tissue-resident memory T cells in the joint.
Cell Rep. 2021 Oct 26;37(4):109902. doi: 10.1016/j.celrep.2021.109902.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验