Iorio A M, Neri M, Enrico P, Goldin A, Bonmassar E
Int J Cancer. 1981 Oct 15;28(4):497-502. doi: 10.1002/ijc.2910280416.
Lymphoma EL-4 of B6 origin was inoculated into lethally-irradiated syngeneic B6 or resistant BD2F1 hybrid recipients. Marked impairment of lymphoma cell proliferation (i.e. hybrid resistance, HR) occurred in the spleen but not in the liver or lung of BD2F1 hosts. Treatment with DTIC at the optimal dose of 80 mg/kg i.p. produced inhibitory effects in spleen, liver and lung of young BD2F1 mice, that were much greater than those observed in syngeneic B6 hosts. Increased anti-lymphoma effects for HR and DTIC chemotherapy were not detectable in the liver or lung of old BD2F1 mice or in the spleen, liver or lung of young hybrid recipients depressed for HR by pretreatment with cyclophosphamide. This is the first report on combined antileukemic effects of the host's anti-tumor natural resistance and chemotherapy.
将源自B6的淋巴瘤EL-4接种到经致死剂量照射的同基因B6或抗性BD2F1杂交受体中。在BD2F1宿主的脾脏中出现了淋巴瘤细胞增殖的显著受损(即杂交抗性,HR),但在肝脏或肺中未出现。以80mg/kg腹腔注射的最佳剂量使用达卡巴嗪进行治疗,对年轻BD2F1小鼠的脾脏、肝脏和肺产生了抑制作用,这些作用远大于在同基因B6宿主中观察到的作用。在老龄BD2F1小鼠的肝脏或肺中,或者在用环磷酰胺预处理使HR降低的年轻杂交受体的脾脏、肝脏或肺中,均未检测到HR和达卡巴嗪化疗联合产生的增强抗淋巴瘤作用。这是关于宿主抗肿瘤天然抗性和化疗联合抗白血病作用的首篇报道。