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血液系统恶性肿瘤中T细胞受体δ链基因分析

[Analysis of T-cell receptor delta chain gene in hematological malignancies].

作者信息

Kimura N, Akiyoshi T

机构信息

First Department of Internal Medicine, Fukuoka University School of Medicine.

出版信息

Nihon Rinsho. 1992 Jun;50(6):1309-14.

PMID:1325569
Abstract

We analyzed the rearrangement of T-cell receptor (TcR) delta chain gene in 196 cases of hematological malignancies. This rearranged band (s) was observed in 15% of the total cases investigated. All T-ALL patients and cell lines, except for P30/Okubo, had a new band (s) or deletion of J delta 1 gene locus, indicating the gamma delta T-cell type or the alpha beta T-cell type. In the other T-cell malignancies, the delta rearranged band (s) was recognized in 5% of T-cell lymphomas, 20% of AILD but not in ATL, Hodgkin's disease, T-CLL. Inappropriate delta rearrangement was frequently recognized in 63% of B-ALL and 50% of CML-BC but none or few (5% less) in B-CLL, B-lymphoma and AML. Southern blotting, using J delta 1 and V delta gene probes or Pst I enzyme digestion, indicated that the inappropriate delta rearranged band in B-ALL and CML-BC is V delta 2D or DD without a J delta locus. The rearranged band (s) involved J delta locus, was mostly recognized in 5/6 cases of CD7 (+) stem cell leukemia. Therefore, the TcR delta gene is useful in evaluating clonality for the most immature T-cell neoplasms, not showing rearrangement of the other TcR genes. Moreover, this delta gene may be a useful tool for distinguishing T-lineage from the other lineages, using the characteristic rearrangement pattern (V delta 2D as a inappropriate pattern, or (D) DJ and V (D) DJ as the T-lineage pattern (s)).

摘要

我们分析了196例血液系统恶性肿瘤患者的T细胞受体(TcR)δ链基因重排情况。在所研究的全部病例中,15%观察到了这种重排条带。除P30/Okubo外,所有T-ALL患者及细胞系均出现了新的条带或Jδ1基因位点缺失,提示为γδT细胞型或αβT细胞型。在其他T细胞恶性肿瘤中,5%的T细胞淋巴瘤、20%的AILD出现了δ重排条带,但在ATL、霍奇金病、T-CLL中未出现。63%的B-ALL和50%的CML-BC中频繁出现不适当的δ重排,但在B-CLL、B淋巴瘤和AML中未出现或仅有少数(5%以下)出现。使用Jδ1和Vδ基因探针或Pst I酶切进行Southern印迹分析表明,B-ALL和CML-BC中不适当的δ重排条带为无Jδ位点的Vδ2D或DD。涉及Jδ位点的重排条带,在5/6的CD7(+)干细胞白血病病例中大多可识别。因此,TcRδ基因对于评估最不成熟的T细胞肿瘤的克隆性很有用,这些肿瘤未显示其他TcR基因的重排。此外,利用特征性重排模式(Vδ2D为不适当模式,或(D)DJ和V(D)DJ为T系模式),该δ基因可能是区分T系与其他谱系的有用工具。

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