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CD7(+)急性白血病的生物学特征

Biological characteristics of CD7(+) acute leukemia.

作者信息

Miwa H, Nakase K, Kita K

机构信息

Second Department of Internal Medicine, Mie University School of Medicine, Tsu, Japan.

出版信息

Leuk Lymphoma. 1996 Apr;21(3-4):239-44.

PMID:8726405
Abstract

Eighty six of 430 acute myeloblastic leukemia (AML) patients (20.0%) and forty of 173 acute lymphoblastic leukemia (ALL) patients (23.1%) had CD7 on their leukemia cells. CD7(+) AML occurred at a younger age than CD7(-) AML, and is more frequent in males. Hepatomegaly and central nervous system involvement were also more frequent in CD7(+) AML than in CD7(-) AML. The age of onset of CD7(+) ALL is also younger than that of CD7(-) ALL. Phenotypically, CD(+) AML expressed CD34, HLA-DR, and TdT more frequently than CD7(-) AML while CD7(+) ALL expressed CD13/33 more often than CD7(-) ALL cells responded most significantly to interleukin 3 (IL-3), whereas most CD7(-) AML cells responded more significantly to granulocyte macrophage-colony stimulating factor (GM-CSF) and/or granulocyte (G)-CSF than to IL-3. CD7(+)sCD3(-)CD4(-)CD8(-) ALL expressed G-CSF receptor and c-kit mRNA more frequently, which is not usual in other types of ALL. P-glycoprotein (P-gp)/multi-drug resistance gene (MDR1), thought to be expressed in hematopoietic stem cells, is expressed in CD7(+) AML and CD7(+)sCD3(-) CD4(-)CD8(-) ALL significantly more often than in CD7(-) acute leukemias and the CR rate and overall survival of CD7(+)AML was worse than CD7(-) AML. These data, collectively, suggest the close association of CD7(+) AML and CD7(+)sCD3(-)CD4(-)CD8(-) ALL, not only the common expression of CD7 itself but also because their phenotypical immaturity, cytokine receptor expression, P-gp/MDR1 expression and clinical manifestations including the frequent occurrence in males and the poor prognosis. We propose that CD7(+) acute leukemia is an hematopoietic stem cell leukemia which may be separate entity.

摘要

430例急性髓细胞白血病(AML)患者中有86例(20.0%),173例急性淋巴细胞白血病(ALL)患者中有40例(23.1%)白血病细胞表达CD7。CD7(+) AML发病年龄比CD7(-) AML小,且在男性中更常见。肝肿大和中枢神经系统受累在CD7(+) AML中也比CD7(-) AML更常见。CD7(+) ALL的发病年龄也比CD7(-) ALL小。表型上,CD(+) AML比CD7(-) AML更频繁地表达CD34、HLA-DR和TdT,而CD7(+) ALL比CD7(-) ALL更频繁地表达CD13/33。大多数CD7(+)细胞对白细胞介素3(IL-3)反应最显著,而大多数CD7(-) AML细胞对粒细胞巨噬细胞集落刺激因子(GM-CSF)和/或粒细胞(G)-CSF的反应比对IL-3更显著。CD7(+)sCD3(-)CD4(-)CD8(-) ALL更频繁地表达G-CSF受体和c-kit mRNA,这在其他类型的ALL中并不常见。被认为在造血干细胞中表达的P-糖蛋白(P-gp)/多药耐药基因(MDR1),在CD7(+) AML和CD7(+)sCD3(-) CD4(-)CD8(-) ALL中的表达明显比在CD7(-)急性白血病中更频繁,且CD7(+)AML的完全缓解率和总生存率比CD7(-) AML更差。这些数据共同表明CD7(+) AML和CD7(+)sCD3(-)CD4(-)CD8(-) ALL密切相关,不仅因为CD7本身的共同表达,还因为它们的表型不成熟、细胞因子受体表达、P-gp/MDR1表达以及包括男性中频繁发生和预后不良在内的临床表现。我们提出CD7(+)急性白血病是一种造血干细胞白血病,可能是一个独立的实体。

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