Merritt J A, Meltzer D M, Ball L A, Borden E C
Prog Clin Biol Res. 1985;202:423-30.
The interferon-induced enzyme 2-5A synthetase was measured in extracts of ficoll-purified peripheral mononuclear cells from normal healthy volunteers and a large group of patients with metastatic carcinoma. The range of values in both populations was very large and overlapped considerably. On average, individuals with disseminated cancer have a two-fold increase in 2-5A synthetase activity. In addition, several patients have been identified who appear to have fully induced 2-5A synthetase activity with no detectable serum interferon and no history of prior interferon injections. This indicates that the interferon regulated 2-5A system is activated in metastatic carcinoma. Treatment of patients with interferon-alpha caused a dose-dependent increase in enzyme activity. The maximum fold increase varied from individual to individual, as did the dose required for maximum enzyme stimulation. A rigorous attempt must now be made to correlate enzyme induction with the clinical outcome of interferon treatment in order to assess the clinical value of such measurements.
在从正常健康志愿者以及一大群转移性癌患者中通过菲可分离法纯化得到的外周血单个核细胞提取物中,对干扰素诱导酶2-5A合成酶进行了检测。这两组人群中的酶活性值范围都非常大,且有相当程度的重叠。平均而言,患有播散性癌症的个体其2-5A合成酶活性会增加两倍。此外,还发现了几名患者,他们似乎具有完全诱导的2-5A合成酶活性,但血清中检测不到干扰素,且既往也没有注射过干扰素的病史。这表明在转移性癌中,干扰素调节的2-5A系统被激活。用α干扰素治疗患者会导致酶活性呈剂量依赖性增加。最大增加倍数因个体而异,达到最大酶刺激所需的剂量也因个体不同而有所差异。现在必须进行严格的尝试,将酶诱导与干扰素治疗的临床结果相关联,以便评估此类检测的临床价值。