Interferon protects normal human granulocyte/macrophage colony-forming cells from Ara-C cytotoxicity.

C M Richman, C A Slapak, B Toh
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Abstract

Interferons (IFN) have clinical efficacy in certain hematologic malignancies. Combining IFN with conventional cytotoxic agents has been proposed as a means of improving therapy for diseases such as chronic myelogenous leukemia (CML). In this study, we examined the effect of recombinant interferons alone and in combination with Ara-C on normal and leukemic human hematopoietic progenitor cells (CFU-GM) in vitro. Mononuclear cells from normal bone marrow, peripheral blood of patients with CML, or the acute nonlymphocytic leukemia cell line HL-60 were incubated with alpha-, beta-, or gamma-IFN (0-1,000 units/ml) followed by the addition of Ara-C. The survival of normal CFU-GM was significantly increased if cells were treated with IFN 1 h before 3 h of Ara-C exposure. Similar IFN pretreatment of CML and HL-60 progenitors failed to protect leukemic CFU-GM from Ara-C-induced toxicity. This selective protection of normal CFU-GM may have clinical application.

干扰素保护正常人粒细胞/巨噬细胞集落形成细胞免受Ara-C细胞毒性。
干扰素(IFN)在某些血液系统恶性肿瘤中具有临床疗效。IFN与常规细胞毒性药物联合已被提出作为改善慢性粒细胞白血病(CML)等疾病治疗的一种手段。在这项研究中,我们检测了重组干扰素单独使用和与Ara-C联合使用对体外正常和白血病人造血祖细胞(CFU-GM)的影响。用α -、β -或γ - ifn(0- 1000单位/ml)孵育来自正常骨髓、CML患者外周血或急性非淋巴细胞白血病HL-60细胞系的单个核细胞,然后加入Ara-C。正常CFU-GM细胞在暴露Ara-C 3小时前1小时用IFN处理,可显著提高细胞存活率。类似的IFN预处理CML和HL-60祖细胞未能保护白血病CFU-GM免受ara - c诱导的毒性。这种对正常CFU-GM的选择性保护可能具有临床应用价值。
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