Pedersen B K, Bygbjerg I C, Theander T G, Andersen B J
Allergy. 1986 Sep;41(7):537-42. doi: 10.1111/j.1398-9995.1986.tb00340.x.
Natural killer (NK) cell activity against K 562 target cells was inhibited by pharmacological concentrations of chloroquine, mefloquine and quinine. The most potent were mefloquine and quinine. The drug-induced inhibition of the NK cell activity was abolished by addition of alpha-interferon (IF) or interleukin 2 (Il-2); preincubation of mononuclear cells with IF or Il-2 followed by addition of anti-malarial drugs decreased the inhibitory effects of the drugs. The drug-induced inhibition of the NK cell activity was not dependent on the presence of monocytes. Using monocyte depleted Percoll fractionated NK cell enriched populations in a single cell agarose assay, it was shown that the inhibitory effects of mefloquine, but not of chloroquine and quinine were due to an inhibition of the formation of effector/target cell conjugates.
氯喹、甲氟喹和奎宁的药理浓度可抑制自然杀伤(NK)细胞对K562靶细胞的活性。其中最有效的是甲氟喹和奎宁。添加α干扰素(IF)或白细胞介素2(Il-2)可消除药物诱导的NK细胞活性抑制;单核细胞先用IF或Il-2预孵育,然后添加抗疟药物,可降低药物的抑制作用。药物诱导的NK细胞活性抑制不依赖于单核细胞的存在。在单细胞琼脂糖试验中,使用经Percoll分级分离的去除单核细胞的富含NK细胞群体,结果显示甲氟喹而非氯喹和奎宁的抑制作用是由于效应细胞/靶细胞结合物形成受到抑制。