Pastore S, De Vecchis L, Migliorati G, Frati L, Bonmassar A G
J Immunopharmacol. 1982;4(3):183-97. doi: 10.3109/08923978209026433.
Vindesine (VDS), a structural analogue of Vinca Alkaloids, was found to increase the NK-mediated cytolytic effects of mouse lymphocytes against human K562 target cells in a 18-hr assay. Pretreatment of effector or target cells with the drug did not affect substantially the NK reaction. The phenomenon has been detected using splenocytes of either congenitally athymic or conventional euthymic mice of different strains. Effector lymphocytes deprived of cells adherent to plastic surface or to nylon-wool column were still competent for drug-mediated increase of NK function. It is suggested that modification of the membrane make-up of effector or target cells reversibly induced by VDS, would promote higher NK-mediated cytolytic effects.
长春地辛(VDS)是一种长春花生物碱的结构类似物,在一项18小时的实验中发现它能增强小鼠淋巴细胞对人K562靶细胞的自然杀伤(NK)介导的细胞溶解作用。用该药物对效应细胞或靶细胞进行预处理,对NK反应没有实质性影响。使用不同品系的先天性无胸腺或常规有胸腺小鼠的脾细胞均检测到了这一现象。去除附着在塑料表面或尼龙毛柱上的细胞后的效应淋巴细胞,仍能使药物介导的NK功能增强。提示VDS可逆性诱导效应细胞或靶细胞膜组成的改变,可促进更高的NK介导的细胞溶解作用。