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慢性粒细胞白血病(CML)的原始细胞危象。II. “淋巴细胞样”和髓细胞样病例的细胞表面标志物分析。

Blast crisis of chronic myeloid leukaemia (CML). II. Cell surface marker analysis of "lymphoid" and myeloid cases.

作者信息

Janossy G, Greaves M F, Revesz T, Lister T A, Roberts M, Durrant J, Kirk B, Catovsky D, Beard M E

出版信息

Br J Haematol. 1976 Oct;34(2):179-92. doi: 10.1111/j.1365-2141.1976.tb00189.x.

Abstract

Fourteen cases of philadelphia chromosome (Ph1) positive chronic myeloid leukaemia in blast transformation have been investigated using cell surface markers. Morphologically eight cases were lymphoid and the remainder myeloid in appearance. All cases were negative with surface markers for thymocytes and T and B lymphocytes. Five of the lymphoid cases reacted with an antiserum specific for acute lymphoid leukaemia )ALL) of non-T non-B type and were also weakly reactive with a lymphocyte reactive antiserum. A sixth patient, whose blast cells were anti-ALL negative (ALL-) at presentation, subsequently developed central nervous system leukaemia with anti-ALL positive (ALL+) blast cells in the CSF. In all cases the leukaemic blast cells showed greatly diminished expression of cholera toxin receptors when compared to granulocytic cells from the chronic phase of CML. This parallels weak or negligible expression of the cholera toxin receptor in ALL and AML. These results suggest that the blastic phase of CML may involve different cellular derivatives of a pluripotential stem cell in which the primary malignant/genetic changes reside. The blast crisis of CML can therefore be heterogeneous with respect to cellular expression and in a significant proportion of patients involves a cell which is by membrane markers and morphological criteria indistinguishable from that seen in the common form of ALL. In these cases the Philadelphia chromosome may be the only distinguishing cellular characteristic.

摘要

应用细胞表面标志物对14例费城染色体(Ph1)阳性的慢性髓性白血病急变期患者进行了研究。形态学上,8例为淋巴样,其余为髓样。所有病例的胸腺细胞、T淋巴细胞和B淋巴细胞表面标志物均为阴性。5例淋巴样病例与一种针对非T非B型急性淋巴细胞白血病(ALL)的抗血清发生反应,并且与一种淋巴细胞反应性抗血清也有弱反应。第六例患者,其原始细胞在初诊时为抗ALL阴性(ALL-),随后发生中枢神经系统白血病,脑脊液中的原始细胞为抗ALL阳性(ALL+)。与慢性期慢性髓性白血病的粒细胞相比,所有病例的白血病原始细胞霍乱毒素受体表达均显著降低。这与ALL和AML中霍乱毒素受体的弱表达或无表达情况相似。这些结果提示,慢性髓性白血病急变期可能涉及多能干细胞的不同细胞衍生物,其中存在原发性恶性/基因改变。因此,慢性髓性白血病的急变期在细胞表达方面可能是异质性的,并且在相当比例的患者中涉及一种通过膜标志物和形态学标准与常见ALL形式中所见细胞无法区分的细胞。在这些病例中,费城染色体可能是唯一可区分的细胞特征。

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