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首页> 外文期刊>Hematological oncology >Pattern of T-cell receptor delta gene rearrangement by Southern blotting and polymerase chain reaction technique in Hong Kong Chinese patients with non-T-cell hematological malignancies.
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Pattern of T-cell receptor delta gene rearrangement by Southern blotting and polymerase chain reaction technique in Hong Kong Chinese patients with non-T-cell hematological malignancies.

机译:通过Southern印迹和聚合酶链反应技术在香港中国非T细胞血液系统恶性肿瘤患者中T细胞受体δ基因重排的模式。

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摘要

It has been recognized that clonal T-cell receptor delta (TCR delta) gene rearrangement is present in both T-and B-cell malignancies. The highly sensitive polymerase chain reaction (PCR) technique may be applicable to cases of leukemia and lymphoma of non-T-cell origin for detection of minimal residual disease (MRD). A PCR technique was used in this study to investigate the pattern of clonal TCR delta gene rearrangement in Hong Kong Chinese patients with non-T-cell hematological malignancies. Seventy-three patients with the diagnosis of acute leukemia and non-Hodgkin's lymphoma of non-T-cell origin were included in this study. There were 20 patients with common ALL (cALL), seven precursal B-cell ALL (PreB-ALL), 23 acute myeloid leukemia (AML), and 23 non-Hodgkin's lymphoma of B-lineage (B-NHL). Clonal rearrangement was detectable by Southern analysis using a J delta 1 probe in 41 per cent of ALL of B-lineage but in none of the B-NHL or AML. The samples were also studied further by monoclonal PCR amplification for TCR delta gene rearrangement. Three different sets of primers were employed to detect clonal rearrangement of the TCR delta gene. The V delta 1(D)J delta 1 recombination typically seen in T-cell malignancies were not seen in any of the of the non-T-cell malignancies. The V delta 2 (D) D delta 3 recombination was found exclusively in ALL of B-lineage and was seen in 73 per cent of the Southern positive cases. Although clonal TCR delta gene rearrangement was undetectable by Southern analysis in our AML cases, 26 per cent had a V delta 2(D)J delta 1 recombination found by the PCR technique. Sensitivity of the PCR technique was determined by serial mixing and was up to 5-10 leukemic cells per 10(4) nucleated cells. It was apparent from this study that it was feasible to detect clonal TCR delta gene rearrangement by the PCR technique in a proportion of the cases of non-T-cell hematological malignancies. The PCR technique can be applied to detect residual leukemic cells in marrow of patients in anapparent morphological complete remission. The value of this application requires further clinical evaluation and correlation.
机译:已经认识到,在T细胞和B细胞恶性肿瘤中都存在克隆性T细胞受体δ(TCRδ)基因重排。高度敏感的聚合酶链反应(PCR)技术可能适用于非T细胞来源的白血病和淋巴瘤病例,以检测最小残留疾病(MRD)。在这项研究中使用了一种PCR技术来研究中国香港非T细胞血液系统恶性肿瘤患者的克隆TCR delta基因重排的模式。本研究纳入了73例诊断为急性白血病和非T细胞源性非霍奇金淋巴瘤的患者。有20例常见ALL(cALL),7例前体B细胞ALL(PreB-ALL),23例急性骨髓性白血病(AML)和23例B型非霍奇金淋巴瘤(B-NHL)患者。使用J delta 1探针通过Southern分析可检测到41%的B谱系中的克隆重排,但没有检测到B-NHL或AML中的克隆重排。还通过单克隆PCR扩增对样品进行了TCRδ基因重排的进一步研究。使用三组不同的引物来检测TCRδ基因的克隆重排。通常在T细胞恶性肿瘤中见到的V delta 1(D)J delta 1重组在任何非T细胞恶性肿瘤中均未见。 V delta 2(D)D delta 3重组仅在所有B谱系中发现,在73%的南部阳性病例中可见。尽管在我们的AML病例中,无法通过Southern分析检测到克隆的TCR delta基因重排,但有26%的患者通过PCR技术发现了V delta 2(D)J delta 1重组。 PCR技术的灵敏度通过连续混合确定,每10(4)个有核细胞最多可容纳5-10个白血病细胞。从这项研究中可以明显看出,在一定比例的非T细胞血液学恶性肿瘤病例中,通过PCR技术检测克隆的TCR delta基因重排是可行的。 PCR技术可用于检测形态学上完全缓解的患者骨髓中残留的白血病细胞。此应用程序的价值需要进一步的临床评估和相关性。

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