Provinciali M, Di Stefano G, Raffaeli W, Pari G, Desiderio F, Fabris N
Gerontol. Res. Dept. Italian Natl. Res. Ctrs. on Aging, INRCA, Ancona, Italy.
Int J Neurosci. 1991 Jul;59(1-3):127-33. doi: 10.3109/00207459108985455.
The cytotoxic activity of Natural Killer (NK) and Lymphokine Activated Killer (LAK) cells in neoplastic patients with or without antalgic treatment was studied. NK cell activity was found reduced in untreated neoplastic patients when compared to healthy subjects. The atalgic treatment with morphine (orally or intrathecally administered) was able to significantly reduce the mean values of NK cell activity found in cancer patients. In three patients the cytotoxicity of NK cells significantly decreased during transfer from oral to intrathecal administration of morphine. In contrast to the NK cell function, the development of LAK cell activity significantly increased in neoplastic patients when compared to healthy controls. Further increments were obtained during treatment with morphine. The oral treatment with morphine was able to determine a higher induction of LAK cells than the intrathecal administration of the drug. Besides providing new knowledge on the effect of morphine on immune system our findings suggest that, in order to include neoplastic patients in clinical trials of adoptive immunotherapy with LAK cells and interleukin-2 (IL-2), the antalgic therapy with oral administration of morphine may represent a better solution than the intrathecal administration of the drug.
研究了接受或未接受镇痛治疗的肿瘤患者中自然杀伤(NK)细胞和淋巴因子激活的杀伤(LAK)细胞的细胞毒性活性。与健康受试者相比,发现未接受治疗的肿瘤患者的NK细胞活性降低。吗啡(口服或鞘内给药)的镇痛治疗能够显著降低癌症患者中发现的NK细胞活性的平均值。在三名患者中,从口服吗啡转为鞘内给药期间,NK细胞的细胞毒性显著降低。与NK细胞功能相反,与健康对照相比,肿瘤患者中LAK细胞活性的发展显著增加。吗啡治疗期间进一步增加。口服吗啡治疗比鞘内给药能够诱导更高水平的LAK细胞。除了提供关于吗啡对免疫系统影响的新知识外,我们的研究结果表明,为了将肿瘤患者纳入LAK细胞和白细胞介素-2(IL-2)过继性免疫治疗的临床试验中,口服吗啡的镇痛治疗可能比鞘内给药是更好的解决方案。