Cesario T C, Slater L M, Kaplan H S, Gupta S, Gorse G J
Cancer Res. 1984 Nov;44(11):4962-6.
Since gamma-interferon (IFN-gamma) is a potent immunomodulator and patients receiving certain antineoplastic agents are at risk of unusual infections, we have determined the effect of certain antineoplastic agents on IFN-gamma production. Induction of peripheral blood mononuclear cells from normal donors in the presence and absence of various antineoplastic agents was achieved using phytohemagglutinin (8 micrograms/ml). Supernatants were then separated by centrifugation, dialyzed, and assayed for interferon. Cell viability was always greater than 85% with or without the presence of drugs. Hydrocortisone was found to eliminate IFN-gamma production if added within 24 hr after the phytohemagglutinin. The suppression of IFN-gamma production occurred with hydrocortisone concentrations as low as 0.65 microgram/ml, was associated with a diminished proliferative response to the lectin, and occurred with other interferon inducers including staphylococcal enterotoxin A. Adriamycin (0.4 microgram/ml) and vincristine (0.08 microgram/ml) also diminished IFN-gamma production, but only if the peripheral blood mononuclear cells were pretreated with the drugs. Methotrexate, 5-fluorouracil, and 6-mercaptopurine failed to influence the yield of IFN-gamma. These results are significantly different from experiments previously reported using alpha- and beta-interferons and suggest an important mechanism by which these drugs can produce immunosuppression.
由于γ干扰素(IFN-γ)是一种强效免疫调节剂,且接受某些抗肿瘤药物治疗的患者有发生罕见感染的风险,我们已经确定了某些抗肿瘤药物对IFN-γ产生的影响。使用植物血凝素(8微克/毫升)在有和没有各种抗肿瘤药物存在的情况下诱导正常供体外周血单个核细胞。然后通过离心分离上清液,透析,并检测干扰素。无论有无药物存在,细胞活力始终大于85%。发现如果在植物血凝素加入后24小时内加入氢化可的松,可消除IFN-γ的产生。氢化可的松浓度低至0.65微克/毫升时即可抑制IFN-γ的产生,这与对凝集素的增殖反应减弱有关,并且在包括葡萄球菌肠毒素A在内的其他干扰素诱导剂存在时也会发生。阿霉素(0.4微克/毫升)和长春新碱(0.08微克/毫升)也会减少IFN-γ的产生,但前提是外周血单个核细胞先用这些药物预处理。甲氨蝶呤、5-氟尿嘧啶和6-巯基嘌呤未能影响IFN-γ的产量。这些结果与先前报道的使用α和β干扰素的实验有显著差异,并提示了这些药物产生免疫抑制作用的一个重要机制。