Soldateschi D, Censini S, de Gori V, Antoni G, Tagliabue A, Boraschi D
Immunobiology. 1984 May;166(3):251-62. doi: 10.1016/S0171-2985(84)80043-1.
Mouse peritoneal M phi and human blood monocytes were assayed for their antitumor activity in vitro with a cytolysis, a cytostasis and a cytotoxicity test performed in parallel. Both natural and stimulus-induced M phi antitumor capacities were assessed. Results indicate that natural cytolytic activity of unstimulated M phi is generally unable to restrict final tumor cell growth, since it is not coupled with cytostatic capacity. In contrast, exposure of M phi in vitro to either MAF or IFN-beta, besides augmenting M phi cytolytic capacity, induced a very significant cytostatic activity and thus efficiently restricted the survival of tumor cells.
通过同时进行的细胞溶解、细胞抑制和细胞毒性试验,检测了小鼠腹膜巨噬细胞和人血单核细胞的体外抗肿瘤活性。评估了天然和刺激诱导的巨噬细胞抗肿瘤能力。结果表明,未刺激的巨噬细胞的天然细胞溶解活性通常无法限制最终肿瘤细胞的生长,因为它与细胞抑制能力无关。相比之下,体外将巨噬细胞暴露于巨噬细胞激活因子(MAF)或β干扰素(IFN-β),除了增强巨噬细胞的细胞溶解能力外,还诱导了非常显著的细胞抑制活性,从而有效地限制了肿瘤细胞的存活。