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Configuration of immunoglobulin and T cell receptor beta and gamma genes in acute myeloid leukaemia: pitfalls in the analysis of 40 cases.

机译:急性髓细胞性白血病中免疫球蛋白和T细胞受体β和γ基因的配置:40例分析中的陷阱。

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摘要

AIMS: To evaluate the overall incidence of immunoglobulin (Ig) and T cell receptor (TCR) beta and gamma gene rearrangements in a series of 40 cases of acute myeloid leukaemia (AML) and to determine whether structural modifications of these genes could be correlated with the abnormal expression of lymphoid markers in malignant cells. METHODS: All cases were classified according to the criteria of the FAB group and immunophenotyped with a panel of monoclonal antibodies reactive with myeloid and lymphoid differentiation antigens. DNA analysis was performed by the method of Southern using probes for the Ig JH, TCR-C beta 1, and TCR-J tau 1 regions. RESULTS: Phenotypic analysis showed that in addition to myeloid markers, 10 cases expressed lymphoid antigens: CD7 in seven (of which three were TdT positive, one CD2 positive, and one CD19 positive) and CD19 in three. Southern blot analysis showed that bands with sizes different from the germ line control were present in the TCR beta genes in 11 cases: in six of 30 with pure myeloid phenotype and in five of 10 of those expressing lymphoid markers. A close observation of the size and patterns of those bands, however, showed that they could be artefactual. Indeed, further analysis showed that they were either due to resistant Eco RI/Hind III sites at the beta locus or to plasmid contamination. Rearranged genes were eventually found in only two of the 40 cases: at the Ig JH region in one of the 30 with pure myeloid phenotype (3.3%) and at the TCR gamma genes in one of 10 with lymphoid markers (10%). CONCLUSIONS: These observations showed that Ig/TCR gene rearrangements were rare in this AML series (overall incidence of 5%) and that they were not significantly more common in cases with aberrant expression of lymphoid markers. The size and pattern of the potential non-germline bands that can be found in these loci must be carefully evaluated.
机译:目的:评价一系列40例急性髓细胞性白血病(AML)患者中免疫球蛋白(Ig)和T细胞受体(TCR)β和γ基因重排的总体发生率,并确定这些基因的结构修饰是否与淋巴样标志物在恶性细胞中的异常表达方法:根据FAB组的标准对所有病例进行分类,并用与骨髓和淋巴样分化抗原有反应性的单克隆抗体进行免疫表型分析。通过Southern方法使用Ig JH,TCR-C beta 1和TCR-J tau 1区域的探针进行DNA分析。结果:表型分析表明,除髓样标记物外,还有10例表达淋巴样抗原:7例CD7(其中3例TdT阳性,1例CD2阳性和1例CD19阳性)和3例CD19。 Southern印迹分析表明,在11例患者中,TCR beta基因中存在大小不同于种系对照的条带:30个中有6个具有纯髓样表型,而10个中有5个表达淋巴样标记。但是,仔细观察这些频段的大小和样式,可以发现它们可能是人造的。确实,进一步的分析表明它们是由于β基因座的抗性Eco RI / Hind III位点或质粒污染所致。最终仅在40例病例中的2例中发现了重排的基因:在30例中有1例的Ig JH区具有纯髓细胞表型(3.3%),在10例中有1例的TCRγ基​​因具有淋巴标记(10%)。结论:这些观察结果表明,在该AML系列中,Ig / TCR基因重排很少见(总发生率为5%),并且在淋巴标记物异常表达的情况下,它们的发生率并不明显。必须仔细评估在这些基因座中发现的潜在非种系带的大小和模式。

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