Foster R S
Cancer Res. 1978 Sep;38(9):2666-72.
We have studied the interaction of Corynebacterium parvum and a variety of cell cycle-specific and cell cycle-nonspecific chemotherapeutic agents on granulocyte-macrophage progenitor cells [colony-forming units culture (CFU-c)] in C57BL/6 mice. In vitro tritiated thymidine suicide studies showed an increased rate of proliferation of bone marrow CFU-c 24 hr after C. parvum injection. In vivo toxicity of cell cycle-specific agents but not of cell cycle-nonspecific agents for bone marrow CFU-c was increased 24 hr after C. parvum injections. The increased numbers of CFU-c in the spleen, induced by C. parvum, were also sensitive to a cell cycle-specific agent for up to 7 days after C. parvum injection. The findings suggest differences in the kinetics of proliferation of splenic compared to bone marrow CFU-c. The relative time of administration of chemotherapy and immunostimulants such as C. parvum will have to be carefully considered in the design of clinical trials.
我们研究了短小棒状杆菌与多种细胞周期特异性和细胞周期非特异性化疗药物对C57BL/6小鼠粒细胞-巨噬细胞祖细胞[集落形成单位培养物(CFU-c)]的相互作用。体外氚标记胸腺嘧啶核苷自杀研究表明,注射短小棒状杆菌24小时后,骨髓CFU-c的增殖速率增加。注射短小棒状杆菌24小时后,细胞周期特异性药物而非细胞周期非特异性药物对骨髓CFU-c的体内毒性增加。短小棒状杆菌诱导的脾脏中CFU-c数量增加,在注射短小棒状杆菌后长达7天内,对细胞周期特异性药物也敏感。这些发现表明,脾脏CFU-c与骨髓CFU-c的增殖动力学存在差异。在设计临床试验时,必须仔细考虑化疗药物和免疫刺激剂(如短小棒状杆菌)的相对给药时间。