Ko H L, Beuth J, Tunggal L, Gil M, Jeljaszewicz J, Pulverer G
Institute of Medical Microbiology and Hygiene, University of Cologne, Germany.
In Vivo. 1994 Mar-Apr;8(2):173-6.
The antiparasitic naphthylurea suramin (SUR) could be shown to exert immunomodulating and antimetastatic activity in BALB/c-mice. Regular intraperitoneal administration of SUR yielded significant weight gain of spleen and significant enhancement of peritoneal macrophage activity in chemiluminescence assays. The number of thymocytes per mg organ weight did not show evident differences in control and SUR treated groups; however, determinations of lymphocyte subsets revealed up-regulation of mature cells expressing helper/inducer (L3T4) or cytotoxic/suppressor (Lyt-2) phenotypes but down-regulation of immature cells presenting both L3T4/Lyt-2 antigens. Accordingly, administration of SUR obviously accelerated murine thymocyte maturation. Counts of BALB/c-mice peripheral blood lymphocytes (PBL) revealed evident (but statistically non-significant) increases after SUR administration. The determination of activated T-cells expressing interleukin (Il-2) receptors further proved that SUR induced a potent immunostimulation since these cells were significantly enhanced after treatment. To evaluate the antimetastatic activity of SUR, sarcoma L-1 cells were intravenously inoculated into BALB/c-mice. In this model system the number of experimental lung metastases significantly decreased, as compared to control mice which received injections of saline solution. Accordingly, SUR can be regarded as an immunomodulating and antimetastatic substance which seems to be promising for clinical trials in oncology.
抗寄生虫萘脲苏拉明(SUR)已被证明在BALB/c小鼠中具有免疫调节和抗转移活性。定期腹腔注射SUR可使脾脏显著增重,并在化学发光试验中显著增强腹腔巨噬细胞活性。每毫克器官重量的胸腺细胞数量在对照组和SUR处理组中未显示明显差异;然而,淋巴细胞亚群的测定显示,表达辅助/诱导(L3T4)或细胞毒性/抑制(Lyt-2)表型的成熟细胞上调,但同时呈现L3T4/Lyt-2抗原的未成熟细胞下调。因此,SUR的给药明显加速了小鼠胸腺细胞的成熟。BALB/c小鼠外周血淋巴细胞(PBL)计数显示,SUR给药后有明显(但统计学上无显著意义)的增加。对表达白细胞介素(Il-2)受体的活化T细胞的测定进一步证明,SUR诱导了强烈的免疫刺激,因为这些细胞在治疗后显著增加。为了评估SUR的抗转移活性,将肉瘤L-1细胞静脉注射到BALB/c小鼠体内。在这个模型系统中,与接受盐水注射的对照小鼠相比,实验性肺转移瘤的数量显著减少。因此,SUR可被视为一种免疫调节和抗转移物质,似乎有望用于肿瘤学的临床试验。