Hirsch R L, Johnson K P
Clin Immunol Immunopathol. 1985 Nov;37(2):236-44. doi: 10.1016/0090-1229(85)90155-2.
Natural killer (NK) cell activity was evaluated in multiple sclerosis (MS) patients during a phase II trial of recombinant interferon-alpha 2 (IFN). Spontaneous NK activity against the K562 myeloid target cell increased significantly during the first week of treatment in the IFN treatment group. However, NK activity was also increased in the placebo treatment group. Long-term administration of IFN caused a decline of NK activity, below the pretreatment values. This decline was not paralleled by a decline in the percentage of Leu-7 cells in the peripheral blood. The ability of IFN to enhance NK activity during treatment was also evaluated. Enhancement of NK activity by IFN was depressed for the duration of the study in the IFN treatment group. After treatment was stopped, IFN enhancement of NK activity returned to the pre-study value. These studies demonstrate that spontaneous and IFN enhanced NK activity are profoundly affected by the administration of recombinant IFN-alpha 2 in MS patients.
在重组干扰素-α2(IFN)的II期试验期间,对多发性硬化症(MS)患者的自然杀伤(NK)细胞活性进行了评估。在IFN治疗组中,治疗的第一周内,针对K562髓系靶细胞的自发NK活性显著增加。然而,安慰剂治疗组的NK活性也有所增加。长期给予IFN导致NK活性下降,低于治疗前值。这种下降与外周血中Leu-7细胞百分比的下降并不平行。还评估了IFN在治疗期间增强NK活性的能力。在IFN治疗组中,在研究期间IFN对NK活性的增强作用受到抑制。治疗停止后,IFN对NK活性的增强作用恢复到研究前的值。这些研究表明,在MS患者中,重组IFN-α2的给药对自发和IFN增强的NK活性有深远影响。