干扰素治疗慢性骨髓性白血病诱导2′-5′低聚腺苷酸合成酶的研究。

Molecular biotherapy Pub Date : 1992-06-01
T Moritz, B Weissmann, B Grünewald, H Hust, G Kummer, N Niederle
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引用次数: 0

摘要

用干扰素- α (ifn - α) (4 × 10(6) IU/m2)单独或联合50微克ifn - γ治疗的慢性粒细胞白血病(CML)患者外周血单个核细胞(PBMCs)和血清中干扰素诱导的2′-5′寡腺苷酸合成酶(2-5 OAS)的活性测定。在IFN治疗开始时,PBMCs中检测到2-5个OAS滴度显著升高(预处理0.03-1.62,中位数0.2;治疗期间0.8-13.14,中位数4.31;22例研究患者)和血清(预处理21-156 pmol/dl,中位数62;治疗期间532-1740 pmol/dl,中位数800;研究了8名患者)。然而,2-5 OAS滴度与临床结果或IFN治疗无关,而且在IFN抵抗期间,PBMCs中2-5 OAS活性升高(中位数3.45;范围1.05 - -13.14;11例患者被检出。这些数据反对2-5 OAS系统直接参与IFN治疗CML的疗效。然而,pbmc或血清中2-5个OAS滴度似乎是生物活性IFN治疗的可靠对照。
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Induction of 2'-5' oligoadenylate synthetase during interferon treatment of chronic myelogenous leukemia.

Activity of the interferon-induced enzyme 2'-5' oligoadenylate synthetase (2-5 OAS) was measured in peripheral blood mononuclear cells (PBMCs) and serum of patients with chronic phase Ph'-positive chronic myelogenous leukemia (CML) treated with interferon-alpha (IFN-alpha) (4 x 10(6) IU/m2) alone or in combination with 50 micrograms IFN-gamma. At the beginning of IFN therapy, marked elevation of 2-5 OAS titers was detected in PBMCs (pretreatment 0.03-1.62, median 0.2; during treatment 0.8-13.14, median 4.31; 22 patients studied) and in serum (pretreatment 21-156 pmol/dl, median 62; during treatment 532-1740 pmol/dl, median 800; eight patients studied). However, 2-5 OAS titers were not related to clinical outcome or IFN therapy and also during IFN resistance elevated 2-5 OAS activity in PBMCs (median 3.45; range 1.05-13.14; 11 patients studied) were detected. These data argue against direct involvement of the 2-5 OAS system in the therapeutic effect of IFN in CML. However, 2-5 OAS titers in PBMCs or serum appear to be a reliable control of biologically active IFN therapy.

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