Tank B, Bijma A M, Marquet R L, Eggermont A M, Weimar W, Jeekel J, Westbroek D L
Oncology. 1985;42(3):157-63. doi: 10.1159/000226023.
10 patients with disseminated colorectal cancer were treated either chronically or cyclically with human recombinant leukocyte A interferon (IFl-rA) for 3 months. During this period, leukocyte adherence inhibition (LAI), natural killer (NK) cell activity, concanavalin A-induced gamma-interferon production capacity (GIPCA) and phytohemagglutinin response were sequentially monitored. In both chronically and cyclically treated patients, IFl-rA therapy led to a 'short-lived' augmentation of NK cell activity. In the chronically treated patients, there was a further depression in the NK cell activity during the course of therapy. The outcome of LAI remained unaltered irrespective of the mode of IFl-rA therapy. There was an inverse correlation between GIPCA and phytohemagglutinin response.
10例播散性结直肠癌患者接受人重组白细胞A干扰素(IFl-rA)长期或周期治疗3个月。在此期间,依次监测白细胞黏附抑制(LAI)、自然杀伤(NK)细胞活性、伴刀豆球蛋白A诱导的γ干扰素产生能力(GIPCA)和植物血凝素反应。在长期和周期治疗的患者中,IFl-rA治疗均导致NK细胞活性“短暂”增强。在长期治疗的患者中,治疗过程中NK细胞活性进一步降低。无论IFl-rA治疗方式如何,LAI结果均未改变。GIPCA与植物血凝素反应呈负相关。