Ellis C N, Kang S, Grekin R C, LoBuglio A F, Voorhees J J
Arch Dermatol. 1985 Jul;121(7):877-80. doi: 10.1001/archderm.121.7.877.
We monitored the antibody-dependent cell-mediated cytotoxicity of polymorphonuclear leukocytes from 14 patients with psoriasis before and during etretinate therapy. Neutrophils obtained from the patients with psoriasis at pretherapy demonstrated significantly greater cytotoxic activity than control cells. After four weeks of etretinate therapy, the cytotoxicity of neutrophils from the psoriatic patients decreased significantly and was no longer significantly different from the control value (at a 1:1 effector-to-target ratio). The decline in neutrophil cytotoxicity preceded significant clearing of our patients' psoriasis. The reduction in the antibody-dependent cell-mediated cytotoxicity of polymorphonuclear leukocytes from patients with psoriasis occurs early during therapy and may represent one of the mechanisms of action of etretinate.
我们监测了14例银屑病患者在阿维A治疗前及治疗期间多形核白细胞的抗体依赖性细胞介导的细胞毒性。治疗前从银屑病患者获取的中性粒细胞表现出比对照细胞显著更强的细胞毒性活性。阿维A治疗四周后,银屑病患者中性粒细胞的细胞毒性显著降低,且与对照值不再有显著差异(效应细胞与靶细胞比例为1:1时)。中性粒细胞细胞毒性的下降先于患者银屑病的显著消退。银屑病患者多形核白细胞的抗体依赖性细胞介导的细胞毒性在治疗早期就降低,这可能代表了阿维A的作用机制之一。