Moody D J, Fahey J L, Durkos-Smith D, Ellison G W, Myers L W
J Immunopharmacol. 1986;8(2):259-69. doi: 10.3109/08923978609028618.
Five multiple sclerosis patients were treated weekly with cytosine arabinoside (araC) on an escalating dose schedule. The dose was initiated at 50 mg/M2 and then increased once each week by 50 mg/M2 (unless toxicity caused delay). Dosage decisions were based on whether or not the antibody-dependent cellular-cytotoxicity (ADCC) or natural killer (NK) cytotoxicity levels had been reduced to a level more than 2 standard deviations below the control range. Cytosine arabinoside treatment was discontinued in 2 of 5 subjects at doses of 500 mg/M2 due to toxicity. The 3 remaining patients demonstrated sustained reductions in the percentage of FcR+ cells in their peripheral blood. The maximum percentage reductions from the baseline values ranged from 50% to 76%. Concomitant reductions in the NK activity at the same doses ranged from 65% to 83%. ADCC activity in all 3 patients, however, was relatively resistant to suppression. The nadirs for the ADCC activity were only 16% to 44% below the baseline minimum. AraC was shown to reduce the proportion of FcR+ cells and NK cytotoxic activity in preference to ADCC activity.
五名多发性硬化症患者按照剂量递增方案每周接受阿糖胞苷(araC)治疗。剂量从50mg/M²开始,然后每周增加50mg/M²(除非毒性导致延迟)。剂量决策基于抗体依赖性细胞毒性(ADCC)或自然杀伤(NK)细胞毒性水平是否已降至比对照范围低2个标准差以上的水平。由于毒性,5名受试者中有2名在剂量达到500mg/M²时停止了阿糖胞苷治疗。其余3名患者外周血中FcR+细胞百分比持续下降。相对于基线值的最大百分比下降范围为50%至76%。相同剂量下NK活性的相应下降范围为65%至83%。然而,所有3名患者的ADCC活性相对不易被抑制。ADCC活性的最低点仅比基线最小值低16%至44%。阿糖胞苷显示出优先降低FcR+细胞比例和NK细胞毒性活性而非ADCC活性。