Richman C M, Slapak C A, Toh B
Department of Medicine, Thomas Hazen Thorne Bone Marrow Transplant Center, Rush Medical College, Chicago, Illinois.
J Biol Response Mod. 1990 Dec;9(6):570-5.
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(IFN)在某些血液系统恶性肿瘤中具有临床疗效。有人提出将干扰素与传统细胞毒性药物联合使用,作为改善慢性粒细胞白血病(CML)等疾病治疗方法的一种手段。在本研究中,我们在体外研究了重组干扰素单独使用以及与阿糖胞苷(Ara-C)联合使用对正常和白血病人类造血祖细胞(CFU-GM)的影响。将来自正常骨髓、CML患者外周血或急性非淋巴细胞白血病细胞系HL-60的单核细胞与α-、β-或γ-干扰素(0 - 1000单位/毫升)一起孵育,随后加入阿糖胞苷。如果在阿糖胞苷暴露3小时前1小时用干扰素处理细胞,正常CFU-GM的存活率会显著提高。对CML和HL-60祖细胞进行类似的干扰素预处理未能保护白血病CFU-GM免受阿糖胞苷诱导的毒性。对正常CFU-GM的这种选择性保护可能具有临床应用价值。