Yoneda N, Tatsumi E, Teshigawara K, Nagata S, Nagano T, Kishimoto Y, Kimura T, Yasunaga K, Yamaguchi N
Department of Laboratory Medicine, Kobe University School of Medicine, Japan.
Am J Hematol. 1994 Apr;45(4):310-20. doi: 10.1002/ajh.2830450408.
The gene expression of myeloperoxidase (MPO), CD3 epsilon, and CD3 delta molecules, the gene rearrangement of T-cell receptor (TCR) delta, gamma, and beta and immunoglobulin heavy (IgH) chain, and the expression of cell-surface antigens were investigated in seven cases of CD7+ CD5- CD2- and four cases of CD7+ CD5+ CD2- acute lymphoblastic leukemia or lymphoblastic lymphoma (ALL/LBL) blasts, which were negative for cytochemical myeloperoxidase (cyMPO). More mature T-lineage blasts were also investigated in a comparative manner. In conclusion, the CD7+ CD5- CD2- blasts included four categories: undifferentiated blasts without lineage commitment, T-lineage blasts, T-/myeloid lineage blasts, and cyMPO-negative myeloblasts. The CD7+ CD5+ CD2- blasts included two categories; T-lineage and T-/myeloid lineage blasts. The 11 cases were of the germ-line gene (G) for TCR beta and IgH. Four cases were G for TCR delta and TCR gamma. The others were of the monoclonally rearranged gene (R) for TCR delta and G for TCR gamma or R for both TCR delta and TCR gamma. The expression or in vitro induction of CD13 and/or CD33 antigens correlated with the immaturity of these neoplastic T cells, since it was observed in all 11 CD7+ CD5- CD2- and CD7+ CD5+ CD2-, and some CD7+ CD5+ CD2+ (CD3- CD4- CD8-) cases, but not in CD3 +/- CD4+ CD8+ or CD3+ CD4+ CD8- cases. CD3 epsilon mRNA, but not CD3 delta mRNA, was detected in two CD7+ CD5- CD2- cases, while mRNA of neither of the two CD3 molecules was detected in the other tested CD7+ CD5- CD2- cases. In contrast, mRNA of both CD3 epsilon and CD3 delta were detected in all CD7+ CD5+ CD2- cases, indicating that CD7+ CD5- CD2- blasts at least belong to T-lineage. The blasts of two CD7+ CD5- CD2- cases with entire germ-line genes and without mRNA of the three molecules (MPO, CD3 epsilon, and CD3 delta) were regarded as being at an undifferentiated stage prior to their commitment to either T- or myeloid-lineage. The co-expression of the genes of MPO and CD3 epsilon in a CD7+ CD5- CD2- case MPO, CD3 epsilon, and CD3 delta in a CD7+ CD5+ CD2- case suggested the presence of some overlapping phase for T- and myeloid-lineage commitment during immature stages of differentiation. This helps understand the conversion of some T-ALL/LBL cases to acute myeloblastic leukemia (AML).(ABSTRACT TRUNCATED AT 400 WORDS)
对7例CD7+ CD5- CD2-和4例CD7+ CD5+ CD2-急性淋巴细胞白血病或淋巴细胞淋巴瘤(ALL/LBL)原始细胞进行了研究,这些原始细胞的细胞化学髓过氧化物酶(cyMPO)呈阴性,同时检测了髓过氧化物酶(MPO)、CD3ε和CD3δ分子的基因表达、T细胞受体(TCR)δ、γ和β以及免疫球蛋白重链(IgH)的基因重排,以及细胞表面抗原的表达。还以比较的方式研究了更成熟的T系原始细胞。总之,CD7+ CD5- CD2-原始细胞包括四类:未分化的无谱系定向原始细胞、T系原始细胞、T/髓系原始细胞和cyMPO阴性的髓母细胞。CD7+ CD5+ CD2-原始细胞包括两类:T系和T/髓系原始细胞。11例患者的TCRβ和IgH为种系基因(G)。4例患者的TCRδ和TCRγ为G。其他患者的TCRδ为单克隆重排基因(R),TCRγ为G,或TCRδ和TCRγ均为R。CD13和/或CD33抗原的表达或体外诱导与这些肿瘤性T细胞的不成熟相关,因为在所有11例CD7+ CD5- CD2-和CD7+ CD5+ CD2-以及一些CD7+ CD5+ CD2+(CD3- CD4- CD8-)病例中均观察到,但在CD3+/- CD4+ CD8+或CD3+ CD4+ CD8-病例中未观察到。在2例CD7+ CD5- CD2-病例中检测到CD3ε mRNA,但未检测到CD3δ mRNA,而在其他检测的CD7+ CD5- CD2-病例中未检测到这两种CD3分子的mRNA。相反,在所有CD7+ CD5+ CD2-病例中均检测到CD3ε和CD3δ的mRNA,表明CD7+ CD5- CD2-原始细胞至少属于T系。2例CD7+ CD5- CD2-病例的原始细胞具有完整的种系基因且未检测到三种分子(MPO、CD3ε和CD3δ)的mRNA,被认为处于未分化阶段,尚未定向到T系或髓系。在1例CD7+ CD5- CD2-病例中MPO和CD3ε基因的共表达以及在1例CD7+ CD5+ CD2-病例中MPO、CD3ε和CD3δ的共表达表明,在分化的不成熟阶段,T系和髓系定向存在一些重叠阶段。这有助于理解一些T-ALL/LBL病例向急性髓细胞白血病(AML)的转化。(摘要截断于400字)