T细胞受体
剧目
克隆(编程)
计算生物学
生物
遗传学
计算机科学
T细胞
程序设计语言
免疫系统
声学
物理
作者
Raphaël Genolet,Sara Bobisse,Johanna Chiffelle,Marion Arnaud,Rémy Pétremand,Lise Queiroz,Alexandra Michel,Patrick Reichenbach,Julien Cesbron,Aymeric Auger,Petra Baumgaertner,Philippe Guillaume,Julien Schmidt,Melita Irving,Lana E. Kandalaft,Daniel E. Speiser,George Coukos,Alexandre Harari
标识
DOI:10.1016/j.crmeth.2023.100459
摘要
T cell receptor (TCR) technologies, including repertoire analyses and T cell engineering, are increasingly important in the clinical management of cellular immunity in cancer, transplantation, and other immune diseases. However, sensitive and reliable methods for repertoire analyses and TCR cloning are still lacking. Here, we report on SEQTR, a high-throughput approach to analyze human and mouse repertoires that is more sensitive, reproducible, and accurate as compared with commonly used assays, and thus more reliably captures the complexity of blood and tumor TCR repertoires. We also present a TCR cloning strategy to specifically amplify TCRs from T cell populations. Positioned downstream of single-cell or bulk TCR sequencing, it allows time- and cost-effective discovery, cloning, screening, and engineering of tumor-specific TCRs. Together, these methods will accelerate TCR repertoire analyses in discovery, translational, and clinical settings and permit fast TCR engineering for cellular therapies.
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