Waynforth H B, Magee P N
Br J Cancer. 1974 Dec;30(6):512-23. doi: 10.1038/bjc.1974.230.
N-Nitroso-N-methylurea (NMU) induced a marked dose dependent leucopoenia which was associated with an increased survival of skin allografts in adult rats and in 2 strains of mice. The humoral immune response to NMU as assessed by haemolytic plaque formation and haemagglutination was also much reduced. Dimethylnitrosamine (DMN) which, like NMU is a powerful carcinogen and an alkylating agent, showed no immunosuppressive activity after a single dose in rats on either a normal diet or fed a protein-free diet which enhances kidney tumourigenesis. In mice DMN at a near LD(50) dose (14 mg/kg) had no effect on skin graft survival but did reduce the humoral response. At half this dose level, however, no immunosuppressive effect was seen. The results support the conclusion that the immunosuppressive activity of a chemical carcinogen is not necessarily associated with the expression of its carcinogenicity.
N-亚硝基-N-甲基脲(NMU)可诱导明显的剂量依赖性白细胞减少,这与成年大鼠和两种小鼠品系皮肤同种异体移植的存活时间延长有关。通过溶血空斑形成和血凝反应评估,对NMU的体液免疫反应也显著降低。二甲基亚硝胺(DMN)与NMU一样,是一种强致癌物和烷基化剂,在正常饮食或喂食无蛋白饮食(可增强肾肿瘤发生)的大鼠中,单次给药后未显示出免疫抑制活性。在小鼠中,接近半数致死剂量(14mg/kg)的DMN对皮肤移植存活没有影响,但确实降低了体液反应。然而,在该剂量的一半水平时,未观察到免疫抑制作用。这些结果支持以下结论:化学致癌物的免疫抑制活性不一定与其致癌性的表达相关。