Christensen M, Funder A D, Bendix K, Soerensen F B
University Institute of Pathology, Arhus University Hospital, Arhus Hospital, Arhus, Denmark.
J Clin Pathol. 2006 Jun;59(6):645-54. doi: 10.1136/jcp.2005.025809. Epub 2006 Feb 6.
To compare clonal T cell receptor gamma (TCRgamma) gene rearrangements in frozen and formalin-fixed paraffin wax-embedded (FFPE) tissue, using capillary electrophoresis for use in diagnostics, as T cell lymphomas may be difficult to diagnose by conventional methods.
The DNA for PCR was extracted from frozen and FFPE tissue, cell lines and blood. PCR primers Vgamma1-8, Vgamma9, Vgamma10 or Vgamma11 (5' end labelled) combined with a mixture of JgammaP1/JgammaP/JgammaP2/Jgamma2 (unlabelled) were used. Monoclonal cases were sequenced and clonality, reproducibility, sensitivity and specificity analyses were carried out.
In all cases the molecular test was found to be in agreement with the histological diagnosis. Discrepancies were found between frozen and FFPE tissue in 18 of 56 (32%) tests. The method was highly reproducible. The sensitivity was found to be 0.5% for cell lines and 1% for patient specimens and the specificity 100%. The junctional region between the Vgamma and Jgamma segments was specific for each patient.
Capillary electrophoresis of PCR products from frozen and FFPE tissue is suitable for detecting clonal TCRgamma gene rearrangements. It is important, however, to correlate the results with conventional morphological and immunohistochemical studies.
比较冷冻组织与福尔马林固定石蜡包埋(FFPE)组织中的克隆性T细胞受体γ(TCRγ)基因重排情况,采用毛细管电泳技术用于诊断,因为T细胞淋巴瘤可能难以通过传统方法诊断。
从冷冻组织、FFPE组织、细胞系和血液中提取用于PCR的DNA。使用与JγP1/JγP/JγP2/Jγ2混合物(未标记)结合的Vγ1 - 8、Vγ9、Vγ10或Vγ11(5'端标记)的PCR引物。对单克隆病例进行测序,并进行克隆性、重复性、敏感性和特异性分析。
在所有病例中,分子检测结果均与组织学诊断一致。在56次检测中的18次(32%)发现冷冻组织与FFPE组织之间存在差异。该方法具有高度重复性。细胞系的敏感性为0.5%,患者标本的敏感性为1%,特异性为100%。每个患者的Vγ和Jγ片段之间的连接区具有特异性。
冷冻组织和FFPE组织的PCR产物的毛细管电泳适用于检测克隆性TCRγ基因重排。然而,将结果与传统的形态学和免疫组织化学研究相关联很重要。