Konishi F, Tanaka K, Himeno K, Taniguchi K, Nomoto K
Cancer Immunol Immunother. 1985;19(2):73-8. doi: 10.1007/BF00199712.
When a hot water extract of Chlorella vulgaris (CE) was injected into the peritoneal cavity of BALB/c mice inoculated with syngeneic Meth-A tumor cells, the survival times were strikingly prolonged. Furthermore, peritoneal exudate cells (PEC) rich in polymorphonuclear cells (PMN) obtained from normal mice 24 h after CE injection exhibited an antitumor effect in a Winn-type assay using normal recipients. Such an activity of PEC remained almost intact after T cell or macrophage depletion. However, such PEC did not express an antitumor effect in a Winn-type assay using irradiated recipients. It was suggested that CE-induced PEC, presumably PMN, expressed an antitumor effect in cooperation with a host- or recipient-derived element(s) sensitive to irradiation. The antitumor mechanism of CE may be different from that of OK-432, one of the biological response modifiers.
当将普通小球藻热水提取物(CE)注射到接种了同基因Meth - A肿瘤细胞的BALB/c小鼠的腹腔中时,其存活时间显著延长。此外,在CE注射24小时后从正常小鼠获得的富含多形核细胞(PMN)的腹腔渗出细胞(PEC),在使用正常受体的Winn型试验中表现出抗肿瘤作用。在T细胞或巨噬细胞耗竭后,PEC的这种活性几乎保持不变。然而,在使用经辐照受体的Winn型试验中,这种PEC没有表现出抗肿瘤作用。提示CE诱导的PEC,可能是PMN,与对辐照敏感的宿主或受体来源的元素协同发挥抗肿瘤作用。CE的抗肿瘤机制可能与生物反应调节剂之一的OK - 432不同。