Kalechman Y, Albeck M, Oron M, Sobelman D, Gurwith M, Seghal S N, Sredni B
Department of Life Sciences, Bar Ilan University, Ramat Gan, Israel.
J Immunol. 1990 Sep 1;145(5):1512-7.
Ammonium trichloro(dioxyethylene-O-O')tellurate (AS101) is a new synthetic compound previously described by us as having immunomodulating properties and minimal toxicity. Clinical trials are currently in progress with AS101 on AIDS and cancer patients. We found that AS101 was capable of inducing spleen cells and peritoneal exudate cells to secrete high quantities of CSF and IL-1. Because IL-1 has been previously described as a radioprotector and CSF may induce in vivo the proliferation of hemopoietic cells, we designed the present study in order to evaluate the effects of prolonged in vivo injections of AS101 on protection against lethal doses of irradiation, on the recovery pattern of precursor cells, and on the functioning of bone marrow (BM) and spleen cells of mice undergoing sublethal doses of treatment. We demonstrate that pretreatment with AS101 protects mice from lethal effects of ionizing radiation. AS101 was also found to significantly increase the number of BM and spleen cells, the absolute number of granulocyte macrophage-CFU and the secretion of CSF by BM cells. All were tested 9 days after sublethal dose of irradiation was administered. AS101 was found to have all of these radioprotective effects only when administered to mice before irradiation treatment. Moreover, the compound was found to enhance the proportion of CFU-S that enters the S phase of the cell cycle. These findings indicate that AS101 may be a promising agent to be used in reducing the time needed for reconstitution of hemopoietic cells after irradiation treatment.
三氯(二氧乙烯 - O - O')碲酸铵(AS101)是一种新的合成化合物,我们之前曾描述它具有免疫调节特性且毒性极小。目前AS101正在对艾滋病和癌症患者进行临床试验。我们发现AS101能够诱导脾细胞和腹腔渗出细胞分泌大量的集落刺激因子(CSF)和白细胞介素 - 1(IL - 1)。由于IL - 1之前被描述为一种辐射防护剂,且CSF可能在体内诱导造血细胞增殖,我们设计了本研究,以评估长期体内注射AS101对抵御致死剂量辐射的保护作用、对前体细胞恢复模式的影响,以及对接受亚致死剂量治疗的小鼠骨髓(BM)和脾细胞功能的影响。我们证明,用AS101预处理可保护小鼠免受电离辐射的致死效应。还发现AS101能显著增加BM和脾细胞的数量、粒细胞巨噬细胞集落形成单位(CFU)的绝对数量以及BM细胞分泌CSF的量。所有这些都是在给予亚致死剂量辐射9天后进行测试的。发现只有在辐射治疗前给小鼠施用AS101时,该化合物才具有所有这些辐射防护作用。此外,还发现该化合物能提高进入细胞周期S期的脾集落形成单位(CFU - S)的比例。这些发现表明,AS101可能是一种有前途的药物,可用于缩短辐射治疗后造血细胞重建所需的时间。