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骨髓增生异常综合征进展而来的急性白血病中的白血病相关抑制活性。

Leukemia-associated inhibitory activity in acute leukemia developed from myelodysplastic syndrome.

作者信息

Fukuoka T, Fujita S

机构信息

First Department of Internal Medicine, School of Medicine, Ehime University, Japan.

出版信息

Jpn J Med. 1987 Aug;26(3):314-8. doi: 10.2169/internalmedicine1962.26.314.

Abstract

Clinical responses of patients with acute leukemia (AL) following the myelodysplastic syndrome (MDS) to the standard therapy are poor. It is considered that the greatly decreased hemopoiesis in these cases is responsible for their clinical picture. We studied leukemia-associated inhibitory activity (LIA), which inhibited human granulocyte-macrophage progenitors, in these patients. Peripheral blood (PB) mononuclear cells (MNC) suppressive to granulocyte-macrophage colony formation were present in 3 of 5 cases of de novo AL and in 3 of 4 cases of AL following MDS. The PB MNC-cultured media from these cases also suppressed colony formation. The elution patterns of LIA of these cases were almost identical in gel chromatography. These results suggest that LIA may be responsible for the suppression of normal granulopoiesis in some patients with AL developed from MDS, and that the profound derangement of normal hemopoietic capability in these cases may be due to multiple complex factors.

摘要

骨髓增生异常综合征(MDS)后发生急性白血病(AL)的患者对标准治疗的临床反应较差。据认为,这些病例中造血功能的大幅下降是其临床表现的原因。我们研究了这些患者中抑制人粒细胞-巨噬细胞祖细胞的白血病相关抑制活性(LIA)。5例初发AL患者中有3例以及4例MDS后发生AL的患者中有3例存在抑制粒细胞-巨噬细胞集落形成的外周血(PB)单个核细胞(MNC)。这些病例的PB MNC培养基也抑制集落形成。这些病例的LIA在凝胶色谱中的洗脱模式几乎相同。这些结果表明,LIA可能是导致某些由MDS发展而来的AL患者正常粒细胞生成受抑制的原因,并且这些病例中正常造血能力的严重紊乱可能是由于多种复杂因素所致。

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