Santoni A, Riccardi C, Sorci V, Herberman R B
J Immunol. 1980 May;124(5):2329-35.
Adriamycin, a widely employed anti-neoplastic agent, was found to have either inhibitory or stimulatory effects on NK activity, depending on the site examined. A single i.p. administration of ADM resulted in a rapid increase of cytolytic activity by PEC of various mouse strains. The effector cells appeared to be NK cells, being nonadherent and nonphagocytic; they expressed low amounts of Thy 1.2 antigen and had the same pattern of specificity as splenic NK cells. In contrast to the stimulatory effects of NK activity of PEC, ADM caused a transient dose-dependent depression of NK activity in the spleen, with a peak reduction at day 3 and recovery within a few days thereafter. The depressed NK activity could be reversed by removal of adherent cells by passage through a nylon column. Moreover, ADM induced cytostatic activity against tumor cells by macrophages, suggesting that activated macrophages may be responsible for suppression of splenic NK activity. The possible modulation of the levels of NK activity by ADM-induced macrophages was supported by mixture experiments, in which plastic adherent spleen cells from ADM-treated mice, but not from normal mice, inhibited the NK activity of normal spleen cells.
阿霉素是一种广泛应用的抗肿瘤药物,根据所检测的部位不同,它对自然杀伤(NK)活性有抑制或刺激作用。单次腹腔注射阿霉素会使各种小鼠品系的腹腔渗出细胞(PEC)的细胞溶解活性迅速增加。效应细胞似乎是NK细胞,不具有黏附性和吞噬性;它们表达少量的Thy 1.2抗原,并且与脾NK细胞具有相同的特异性模式。与PEC的NK活性的刺激作用相反,阿霉素会导致脾脏中NK活性出现短暂的剂量依赖性降低,在第3天达到最大降低程度,此后几天内恢复。通过尼龙柱去除黏附细胞可使降低的NK活性恢复。此外,阿霉素诱导巨噬细胞产生针对肿瘤细胞的细胞生长抑制活性,这表明活化的巨噬细胞可能是脾脏NK活性受抑制的原因。混合实验支持了阿霉素诱导的巨噬细胞对NK活性水平的可能调节作用,在该实验中,来自阿霉素处理小鼠而非正常小鼠的塑料黏附脾细胞抑制了正常脾细胞的NK活性。