Yamagishi H, Naito K, Ueda Y, Itoi S, Kohnosu H, Kobayashi M, Kubo H, Matsuda A, Oka T
2nd Dept of Surgery, Kyoto Prefectural University of Medicine, Japan.
Biomed Pharmacother. 1991;45(2-3):117-20. doi: 10.1016/0753-3322(91)90131-c.
The change in cellular immunity by Bestatin (ubenimex) treatment--30 mg/day orally--was investigated in 23 gastrointestinal cancer patients for: 1), functional T cell subsets; 2), IL-2 receptor; 3), PHA-induced blastogenesis; and 4), PPD skin reaction. The absolute number of helper T cells (Th) and cytotoxic T cells (Tc) increased in 74 and 79% of cases, respectively, compared with pretreatment values. On the other hand, the absolute number of suppressor T cells (Ts) decreased in 79% of cases. IL-2 receptor increased in 56% of patients, PHA blastogenesis increased in 67% of patients and PPD skin reaction was elevated in 75% of cases comparing to pretreatment values. These results suggest that Bestatin could increase cellular immunity in cancer patients.
研究了23例胃肠道癌患者口服贝司他汀(乌苯美司)(每日30毫克)后细胞免疫的变化,涉及以下方面:1)功能性T细胞亚群;2)白细胞介素-2受体;3)PHA诱导的淋巴细胞增殖;4)PPD皮肤反应。与治疗前相比,辅助性T细胞(Th)和细胞毒性T细胞(Tc)的绝对数量分别在74%和79%的病例中增加。另一方面,79%的病例中抑制性T细胞(Ts)的绝对数量减少。与治疗前相比,56%的患者白细胞介素-2受体增加,67%的患者PHA诱导的淋巴细胞增殖增加,75%的病例PPD皮肤反应增强。这些结果表明贝司他汀可增强癌症患者的细胞免疫。