Mantovani A, Luini W, Peri G, Vecchi A, Spreafico F
J Natl Cancer Inst. 1978 Nov;61(5):1255-61. doi: 10.1093/jnci/61.5.1255.
Spleen natural killer (NK) activity was investigated in cells from C57BL/6J mice treated with various chemotherapeutic agents; 51Cr-labeled YAC-1 lymphoma cells were used as targets. Treatment with azathioprine (a single injection of 100-400 mg/kg ip or 5 daily doses of 80 mg/kg lp) and cyclophosphamide (a single injection of 50--200 mg/kg ip or 5 daily doses of 25 mg/kg ip) resulted in a marked dose-dependent inhibition of NK activity 2 days later. NK cells recovered rapidly from drug-induced suppression; by 7 days after drug treatment, no difference from control values was observed. Dimethyltriazenoimidazole carboxamide (20--200 mg/kg ip) and adriamycin (10--15 mg/kg iv) did not impair natural cytotoxicity per unit number of lymphoid cells, daunomycin (10 mg/kg iv) caused borderline impairment of NK acitivity, and N-trifluoroacetyl-adriamycin-14-valerate (80 mg/kg iv) markedly suppressed natural cytotoxicity. These results are discussed in light of the known effects of these agents on T-cells, B-cells, and K-cells and on hematopoietic histocompatibility-type reactions.
研究了用各种化疗药物处理的C57BL/6J小鼠细胞中的脾脏自然杀伤(NK)活性;使用51Cr标记的YAC-1淋巴瘤细胞作为靶细胞。用硫唑嘌呤(腹腔注射100 - 400mg/kg单次剂量或腹腔注射80mg/kg每日5次剂量)和环磷酰胺(腹腔注射50 - 200mg/kg单次剂量或腹腔注射25mg/kg每日5次剂量)处理后,2天后导致NK活性出现明显的剂量依赖性抑制。NK细胞从药物诱导的抑制中迅速恢复;药物治疗7天后,未观察到与对照值有差异。二甲基三氮烯咪唑甲酰胺(腹腔注射20 - 200mg/kg)和阿霉素(静脉注射10 - 15mg/kg)不会损害单位数量淋巴细胞的天然细胞毒性,柔红霉素(静脉注射10mg/kg)对NK活性造成临界损害,而N-三氟乙酰阿霉素-14-戊酸酯(静脉注射80mg/kg)显著抑制天然细胞毒性。根据这些药物对T细胞、B细胞、K细胞以及造血组织相容性类型反应的已知作用对这些结果进行了讨论。