Hara J, Benedict S H, Mak T W, Gelfand E W
Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
J Clin Invest. 1987 Dec;80(6):1770-7. doi: 10.1172/JCI113270.
We have analyzed T cell receptor alpha-chain gene configuration using three genomic joining (J) region probes in 64 children with acute lymphoblastic leukemia (ALL). 11 out of 18 T-ALLs were T3 positive; alpha-chain gene rearrangements were demonstrated in only two of 18, indicating that the majority of T-ALLs would have rearrangements involving J alpha segments located upstream of these probes. In contrast, 15 out of 46 B-precursor ALLs showed rearrangements of the alpha-chain gene and J alpha segments located approximately 20-30 kb upstream of the constant region were involved in 13 of these patients. Nine of 15 B-precursor ALLs with rearranged alpha-chain genes had rearrangements of both gamma- and beta-chain genes, whereas the remaining six had no rearrangements of gamma- and beta-chain genes. These findings indicated that alpha-chain gene rearrangement is not specific for T lineage cells and gamma- and/or beta-chain gene rearrangement does not appear essential for alpha-chain gene rearrangement, at least in B-precursor leukemic cells.
我们使用三种基因组连接(J)区探针,对64例急性淋巴细胞白血病(ALL)患儿的T细胞受体α链基因构型进行了分析。18例T-ALL中有11例T3呈阳性;18例中仅2例显示α链基因重排,这表明大多数T-ALL会发生涉及这些探针上游Jα片段的重排。相比之下,46例B前体ALL中有15例显示α链基因重排,其中13例患者涉及位于恒定区上游约20 - 30 kb处的Jα片段。15例α链基因重排的B前体ALL中,9例γ链和β链基因均发生重排,而其余6例γ链和β链基因未发生重排。这些发现表明,α链基因重排并非T系细胞所特有,并且γ链和/或β链基因重排对于α链基因重排似乎并非必不可少,至少在B前体白血病细胞中是如此。