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阿糖胞苷诱导多发性硬化症患者自然杀伤细胞及抗体依赖性细胞毒性功能的变化。

Cytosine arabinoside induced changes in natural killer and antibody dependent cellular cytotoxicity functions in multiple sclerosis patients.

作者信息

Moody D J, Fahey J L, Durkos-Smith D, Ellison G W, Myers L W

出版信息

J Immunopharmacol. 1986;8(2):259-69. doi: 10.3109/08923978609028618.

Abstract

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.

摘要

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。

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