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基于聚合酶链反应的基因扫描技术检测TCRγ链基因重排:提高多例皮肤T细胞淋巴瘤样本的诊断准确性及分析克隆异质性

TCRgamma-chain gene rearrangement by PCR-based GeneScan: diagnostic accuracy improvement and clonal heterogeneity analysis in multiple cutaneous T-cell lymphoma samples.

作者信息

Ponti Renata, Fierro Maria T, Quaglino Pietro, Lisa Bonello, Paola Francia di Celle, Michela Ortoncelli, Paolo Fava, Comessatti Alessandra, Novelli Mauro, Bernengo Maria G

机构信息

Section of Dermatology, Department of Medical Sciences and Human Oncology, University of Turin, Turin, Italy.

出版信息

J Invest Dermatol. 2008 Apr;128(4):1030-8. doi: 10.1038/sj.jid.5701109. Epub 2007 Nov 8.

Abstract

Cutaneous T-cell lymphomas are a heterogeneous group of lymphomas where the tumor population emerges within a multiple subclone pattern ("clonal heterogeneity"). PCR analysis has been shown to be useful in the diagnosis of mycosis fungoides (MF) and Sézary Syndrome (SS). Focusing the attention on clonal heterogeneity, the efficacy of the multiplex/heteroduplex (HD) PCR and the GeneScan (GS) capillary electrophoresis analysis was compared in the early diagnosis of MF/SS, using a multiple sample approach. Indeed, GS demonstrated TCRgamma gene rearrangement (GR) in all the 57 SS (100%) and in 123/146 (84%) of the MF samples, whereas the multiplex/HD PCR was less sensitive. An increase in clonality was observed in connection with both a worsening of the cutaneous disease (79% T1/T2; 100% T3/T4) and an increase in the histopathological score (HS < 5, 76%; HS > or = 5, 94%). Clonal heterogeneity with adjunctive reproducible skin TCRgamma-GRs was also observed. "Clonal instability," with different GRs, was present in a small percentage of patients. Therefore, it can be concluded that GS analysis in TCRgamma-GR is able to improve diagnosis in MF/SS patients and the multiple sample approach is helpful for a correct interpretation of clonal patterns in skin lesions, especially in early-stage MF and in SS skin/blood samples.

摘要

皮肤T细胞淋巴瘤是一组异质性淋巴瘤,肿瘤细胞群体以多种亚克隆模式出现(“克隆异质性”)。聚合酶链反应(PCR)分析已被证明在蕈样肉芽肿(MF)和塞扎里综合征(SS)的诊断中有用。聚焦于克隆异质性,采用多样本方法比较了多重/异源双链(HD)PCR和基因扫描(GS)毛细管电泳分析在MF/SS早期诊断中的效果。事实上,GS在所有57例SS(100%)和146例MF样本中的123例(84%)中显示出TCRγ基因重排(GR),而多重/HD PCR的敏感性较低。随着皮肤疾病的恶化(79% T1/T2;100% T3/T4)和组织病理学评分的增加(HS<5,76%;HS≥5,94%),克隆性增加。还观察到伴有辅助性可重复皮肤TCRγ-GRs的克隆异质性。少数患者存在具有不同GRs的“克隆不稳定性”。因此,可以得出结论,TCRγ-GR的GS分析能够改善MF/SS患者的诊断,多样本方法有助于正确解释皮肤病变中的克隆模式,尤其是在早期MF和SS皮肤/血液样本中。

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