Makino M, Fujiwara M, Watanabe H, Aoyagi T, Umezawa H
Laboratory of Immunology, Niigata University School of Medicine, Japan.
Immunopharmacology. 1987 Oct-Nov;14(2):115-21. doi: 10.1016/0162-3109(87)90036-1.
We examined the suppressive effect of a newly developed antitumor agent, 15-deoxyspergualin (DSP), on the plaque-forming cell responses to various antigens. The intraperitoneal injections of DSP at a dose of 5.0 mg/kg body weight suppressed drastically the development of plaque-forming cells in the spleen of C57BL/6 mice immunized with sheep red blood cells (0.2 ml of a 5% suspension), trinitrophenyl-lipopolysaccharide (1 microgram/mice) and trinitrophenyl-Ficoll (100 micrograms/mice). These suppressive effects were observed when the administration of DSP was started after the injection of antigens. The responsiveness of spleen cells from DSP-treated mice was also checked in in vitro culture. Responsiveness to lipopolysaccharide in vitro was not reduced. Furthermore DSP did not significantly suppress the responsiveness of spleen cells to succinylated concanavalin A or production of interleukin-1 or -2. The results are discussed with regards to the mode of action of DSP on immune responsiveness.
我们研究了一种新开发的抗肿瘤药物15-脱氧精胍菌素(DSP)对针对各种抗原的噬斑形成细胞反应的抑制作用。以5.0mg/kg体重的剂量腹腔注射DSP,可显著抑制用绵羊红细胞(0.2ml 5%悬浮液)、三硝基苯基-脂多糖(1微克/小鼠)和三硝基苯基-菲可(100微克/小鼠)免疫的C57BL/6小鼠脾脏中噬斑形成细胞的产生。当在注射抗原后开始给予DSP时,观察到了这些抑制作用。还在体外培养中检查了经DSP处理的小鼠脾细胞的反应性。体外对脂多糖的反应性未降低。此外,DSP并未显著抑制脾细胞对琥珀酰化伴刀豆球蛋白A的反应性或白细胞介素-1或-2的产生。就DSP对免疫反应性的作用方式对结果进行了讨论。