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T急性淋巴细胞白血病细胞中T细胞受体δ基因的重排不同于B系急性淋巴细胞白血病中发生的重排,且优先涉及一个Vδ基因片段。

Rearrangements of the T cell receptor delta gene in T acute lymphoblastic leukemia cells are distinct from those occurring in B lineage acute lymphoblastic leukemia and preferentially involve one V delta gene segment.

作者信息

Loiseau P, Guglielmi P, Le Paslier D, MacIntyre E, Gessain A, Bories J C, Flandrin G, Chen Z, Sigaux F

机构信息

Laboratoire Central d'Immunologie et d'Histocompatibilité, INSERM U93, Paris, France.

出版信息

J Immunol. 1989 May 1;142(9):3305-11.

PMID:2523429
Abstract

Rearrangement of the TCR-delta gene was studied using J delta, C delta, and V delta probes in 61 cases of acute lymphoblastic leukemia (ALL) and several cases of chronic lymphoid neoplasms to define the specificity and the diversity of rearrangements occurring at the delta locus. TCR-delta rearrangements or deletions were found in all T (33 cases) and B lineage (28 cases) ALL but not in any case of B cell chronic proliferations (13 cases). The restriction patterns of rearrangement were clearly distinct between T and B ALL and use of one V delta probe showed that rearrangement of the V delta IDP2 gene segment which is also productively rearranged in the Peer cell line, occurred frequently in T-ALL but never in B lineage ALL. Studies of WT31 and delta TCS1 antibody reactivity showed that at least 4 of 13 CD3+ T-ALL cases expressed the delta protein. CD4 and/or CD8 Ag expression were observed in some of the gamma delta expressing T-ALL. These data show that particular TCR-delta gene rearrangements occur in neoplastic early B cells and that the combinatorial diversity of TCR-delta rearrangements in T cells is higher than initially expected. In addition this study shows that an important proportion of CD3 positive T-ALL cases express the gamma delta heterodimer.

摘要

使用Jδ、Cδ和Vδ探针研究了61例急性淋巴细胞白血病(ALL)及几例慢性淋巴细胞肿瘤中TCR-δ基因的重排,以确定δ基因座处重排的特异性和多样性。在所有T系(33例)和B系(28例)ALL中均发现了TCR-δ重排或缺失,但在任何B细胞慢性增殖病例(13例)中均未发现。T系和B系ALL的重排限制模式明显不同,使用一种Vδ探针显示,在Peer细胞系中也发生有效重排的Vδ IDP2基因片段重排在T-ALL中频繁发生,而在B系ALL中从未发生。对WT31和δTCS1抗体反应性的研究表明,13例CD3+ T-ALL病例中至少有4例表达δ蛋白。在一些表达γδ的T-ALL中观察到了CD4和/或CD8抗原表达。这些数据表明,特定的TCR-δ基因重排在肿瘤性早期B细胞中发生,并且T细胞中TCR-δ重排的组合多样性高于最初预期。此外,本研究表明,相当一部分CD3阳性T-ALL病例表达γδ异二聚体。

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