Zschiesche W, Fahlbusch B, Schumann I, Tonew E
Agents Actions. 1978 Oct;8(5):515-22. doi: 10.1007/BF02111439.
Tilorone hydrochloride, an interferon inducer in small laboratory animals, was demonstrated to elicit formation of macrophage migration affecting and microbial growth inhibitory cytokines after peroral drug administration to mice. Serum kinetics of the migration inhibitory cytokine resembled those of interferon, exhibiting a peak after about 24 h, whereas the bactericidal cytokine showed a steady increase up to 48 h after drug treatment. Both the factors were found to have molecular weights of 10,000--30,000 daltons as determined by Sephadex G-200 chromatography, to be stable at pH 2 and at 56 degrees C for 30 min, sensitive to chymotrypsin and resistant to RNase digestion. The migration enhancing serum activity could not finally be characterized so far. The physicochemical data are discussed in comparison to those of lymphocyte-derived cytokines. It is suggested that cytokine production may be, at least partially, responsible for the immunological effects of tilorone and possibly contribute to its antiviral action.
盐酸替洛隆是一种在小型实验动物体内的干扰素诱导剂,经证实,给小鼠口服该药后,它能引发影响巨噬细胞迁移的物质以及抑制微生物生长的细胞因子的形成。迁移抑制细胞因子的血清动力学与干扰素相似,在约24小时后出现峰值,而杀菌细胞因子在药物治疗后48小时内呈稳定上升趋势。通过葡聚糖凝胶G - 200层析法测定,这两种因子的分子量均为10,000 - 30,000道尔顿,在pH 2和56℃下30分钟稳定,对胰凝乳蛋白酶敏感,对核糖核酸酶消化有抗性。到目前为止,迁移增强血清活性最终仍无法明确其特征。将这些理化数据与淋巴细胞衍生的细胞因子的数据进行了比较讨论。有人提出,细胞因子的产生可能至少部分地是替洛隆免疫效应的原因,并且可能有助于其抗病毒作用。