Balkwill F R, Moodie E M, Freedman V, Fantes K H
Int J Cancer. 1982 Aug 15;30(2):231-5. doi: 10.1002/ijc.2910300217.
In this paper we describe a model system for looking at the effects of human interferon, IFN, on an established human tumour. Highly purified human IFN derived from lymphoblastoid cells (HuIFN alpha-Namalwa) strongly inhibited the growth of a human breast cancer growing as a xenograft in nude mice. The effect was dose-dependent, required daily treatment for an optimal effect and was time-dependent, little inhibition being seen before 2 weeks of therapy. With the doses used, however, neither tumour regression nor disappearance were seen and on morphological examination, treated tumours appeared as miniatures of control tumours. The inhibition of the tumour by HuIFN alpha-Namalwa appeared to be due to a direct effect on the human cells as this IFN had little effect on the mouse immune system in vitro as measured by NK cells activity. Also HuIFN therapy had no effect on levels of an interferon induced enzyme, 2-5A synthetase, in the mouse spleen cells but stimulated this enzyme in the human tumour.
在本文中,我们描述了一个用于研究人干扰素(IFN)对已建立的人类肿瘤影响的模型系统。从淋巴母细胞中提取的高度纯化的人干扰素(HuIFNα-Namalwa)强烈抑制了作为裸鼠异种移植瘤生长的人类乳腺癌的生长。这种作用具有剂量依赖性,为达到最佳效果需要每日治疗,并且具有时间依赖性,在治疗2周前几乎未见抑制作用。然而,使用这些剂量时,既未观察到肿瘤消退也未观察到肿瘤消失,并且在形态学检查中,经治疗的肿瘤表现为对照肿瘤的缩影。HuIFNα-Namalwa对肿瘤的抑制作用似乎是由于对人类细胞的直接作用,因为通过自然杀伤细胞活性测定,这种干扰素在体外对小鼠免疫系统几乎没有影响。此外,HuIFN治疗对小鼠脾细胞中干扰素诱导酶2-5A合成酶的水平没有影响,但能刺激人类肿瘤中的这种酶。