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CD7+ CD5- CD2-和CD7+ CD5+ CD2-淋巴母细胞的谱系确定:关于髓过氧化物酶、CD3ε和CD3δ的表型、基因型及基因表达的研究

Lineage determination of CD7+ CD5- CD2- and CD7+ CD5+ CD2- lymphoblasts: studies on phenotype, genotype, and gene expression of myeloperoxidase, CD3 epsilon, and CD3 delta.

作者信息

Yoneda N, Tatsumi E, Teshigawara K, Nagata S, Nagano T, Kishimoto Y, Kimura T, Yasunaga K, Yamaguchi N

机构信息

Department of Laboratory Medicine, Kobe University School of Medicine, Japan.

出版信息

Am J Hematol. 1994 Apr;45(4):310-20. doi: 10.1002/ajh.2830450408.

DOI:10.1002/ajh.2830450408
PMID:7513945
Abstract

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)

摘要

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)

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