Ruggiero Eliana, Nicolay Jan P, Fronza Raffaele, Arens Anne, Paruzynski Anna, Nowrouzi Ali, Ürenden Gökçe, Lulay Christina, Schneider Sven, Goerdt Sergij, Glimm Hanno, Krammer Peter H, Schmidt Manfred, von Kalle Christof
Department of Translational Oncology, National Center for Tumor Diseases and German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Division of Immunogenetics, German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Nat Commun. 2015 Sep 1;6:8081. doi: 10.1038/ncomms9081.
Unbiased dissection of T-cell receptor (TCR) repertoire diversity at the nucleotide level could provide important insights into human immunity. Here we show that TCR ligation-anchored-magnetically captured PCR (TCR-LA-MC PCR) identifies TCR α- and β-chain diversity without sequence-associated or quantitative restrictions in healthy and diseased conditions. TCR-LA-MC PCR identifies convergent recombination events, classifies different stages of cutaneous T-cell lymphoma in vivo and demonstrates TCR reactivation after in vitro cytomegalovirus stimulation. TCR-LA-MC PCR allows ultra-deep data access to both physiological TCR diversity and mechanisms influencing clonality in all clinical settings with restricted or distorted TCR repertoires.
在核苷酸水平上对T细胞受体(TCR)库多样性进行无偏分析可为人类免疫提供重要见解。我们在此表明,TCR连接锚定磁捕获PCR(TCR-LA-MC PCR)能够在健康和疾病状态下识别TCRα链和β链的多样性,且不受序列相关或定量限制。TCR-LA-MC PCR可识别趋同重组事件,在体内对皮肤T细胞淋巴瘤的不同阶段进行分类,并证明体外巨细胞病毒刺激后TCR的重新激活。TCR-LA-MC PCR能够在所有TCR库受限或扭曲的临床环境中,实现对生理性TCR多样性以及影响克隆性的机制的超深度数据获取。