Asou N, Matsuoka M, Hattori T, Kawano F, Maeda S, Shimada K, Takatsuki K
Blood. 1987 Mar;69(3):968-70.
Rearrangements of the T cell gamma (T gamma) gene were studied in primary neoplastic cells from 75 patients with leukemia or lymphoma. T gamma gene rearrangements were observed in 19 of 21 T cell neoplasms; 14 of 21 immature B cell leukemias, including 4 out of 5 patients with rearrangements of both immunoglobulin heavy-chain (JH) and T cell receptor beta chain (T beta) genes; none out of 16 nonlymphoid leukemias. Thus, T gamma gene rearrangement is frequently found in immature B cells and is not always found in T cells showing T beta gene rearrangement, but it is not detected in nonlymphoid cells. Furthermore, T gamma gene rearrangement in cells with the germline configuration of the JH and T beta genes was observed. These results indicate that the detection of T gamma gene rearrangement does not allow a clear assignment to a particular lineage. However, an analysis of T gamma gene rearrangement provides a further potential tool to establish the lymphoid cellular origin and clonality of hematologic neoplasms and identify the normal stages of lymphocyte differentiation.
对75例白血病或淋巴瘤患者的原发性肿瘤细胞中的T细胞γ(Tγ)基因重排进行了研究。在21例T细胞肿瘤中的19例中观察到Tγ基因重排;21例未成熟B细胞白血病中的14例,包括5例免疫球蛋白重链(JH)和T细胞受体β链(Tβ)基因均发生重排的患者中的4例;16例非淋巴细胞白血病中均未观察到。因此,Tγ基因重排在未成熟B细胞中常见,在显示Tβ基因重排的T细胞中并非总是出现,但在非淋巴细胞中未检测到。此外,在具有JH和Tβ基因种系构型的细胞中观察到了Tγ基因重排。这些结果表明,Tγ基因重排的检测不能明确归属于特定谱系。然而,Tγ基因重排分析为确定血液肿瘤的淋巴细胞起源和克隆性以及识别淋巴细胞分化的正常阶段提供了一个潜在的工具。