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T 细胞大颗粒淋巴细胞白血病中克隆性的评估:流式细胞术检测 T 细胞受体 Vβ库及 T 细胞受体基因重排

Assessment of clonality in T-cell large granular lymphocytic leukemia: flow cytometric T cell receptor Vβ repertoire and T cell receptor gene rearrangement.

作者信息

Qiu Zhi-Yuan, Shen Wen-Yi, Fan Lei, Wang Li, Yu Hui, Qiao Chun, Wu Yu-Jie, Lu Rui-Nan, Qian Jun, He Guang-Sheng, Xu Wei, Li Jian-Yong

机构信息

Department of Hematology, the First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital , Nanjing , China.

出版信息

Leuk Lymphoma. 2015 Feb;56(2):324-31. doi: 10.3109/10428194.2014.921297. Epub 2014 Jul 17.

Abstract

The usefulness of flow cytometric variable β-chain repertoire (FC-Vβ) and T-cell receptor gene rearrangement (TCR-GR) analyses for differentiating T-cell large granular lymphocytic leukemia (T-LGLL) from reactive T-large granular lymphocyte (T-LGL) lymphocytosis has been insufficiently studied to date. In this study, we analyzed the diagnostic value of TCR-GR and FC-Vβ analysis in T-LGLL, and compared these results. In our study, FC-Vβ analysis was positive in all cases of T-LGLL, and clonality assessment of FC-Vβ had equal sensitivity and specificity to GeneScanning analysis but was more sensitive than heteroduplex analysis. Suspected T-cell clonality can best be addressed by evaluating two TCR targets (TCRβ and TCRγ), either in parallel or consecutively. Signal transducer and activator of transcription 3 (STAT3) mutation may provide a diagnostic tool for classifying some cases of T-LGL lymphocytosis as true T-LGLL. Our results further demonstrate a significant correlation of STAT3 mutation with pure red cell aplasia, neutropenia, hepatomegaly, β2-microglobulin and anemia.

摘要

流式细胞术可变β链库(FC-Vβ)和T细胞受体基因重排(TCR-GR)分析在鉴别T细胞大颗粒淋巴细胞白血病(T-LGLL)与反应性T大颗粒淋巴细胞(T-LGL)淋巴细胞增多症方面的实用性,迄今为止尚未得到充分研究。在本研究中,我们分析了TCR-GR和FC-Vβ分析在T-LGLL中的诊断价值,并比较了这些结果。在我们的研究中,FC-Vβ分析在所有T-LGLL病例中均为阳性,FC-Vβ的克隆性评估与基因扫描分析具有相同的敏感性和特异性,但比异源双链分析更敏感。通过并行或连续评估两个TCR靶点(TCRβ和TCRγ),可以最好地解决疑似T细胞克隆性问题。信号转导和转录激活因子3(STAT3)突变可能为将某些T-LGL淋巴细胞增多症病例归类为真正的T-LGLL提供一种诊断工具。我们的结果进一步证明STAT3突变与纯红细胞再生障碍、中性粒细胞减少、肝肿大、β2-微球蛋白和贫血之间存在显著相关性。

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