Namba M, Ogura T, Hirao F, Azuma I, Yamamura Y
Gan. 1978 Dec;69(6):831-4.
Peritoneal exudate cells (PEC) induced by oil-attached cell-wall skeleton of Mycobacterium bovis BCG (BCG-CWS) in ACI/N rats were tested for their effect on both in vivo and in vitro growth of syngeneic fibrosarcoma cells (AMC-60). Treatment of rats with intraperitoneal injections of BCG-CWS induced regression of syngeneic ascites tumor and increased the number of survivals. Whole PEC and adherent PEC from rats injected intraperitoneally with BCG-CWS inhibited the uptake of tritiated thymidine into the fibrosarcoma cells in an in vitro cytostasis test. This in vitro cytostatic effect was more marked as the ratio of effector to target cells increased. In addition, when tumor cells were inoculated subcutaneously with BCG-CWS activated PEC, tumor takes decreased markedly. Oil-stimulated PEC and normal peritoneal resident cells were inactive in inhibition of tumor growth in vivo and in vitro.
对用牛分枝杆菌卡介苗(BCG)的油附细胞壁骨架(BCG-CWS)诱导的ACI/N大鼠的腹腔渗出细胞(PEC),检测其对同基因纤维肉瘤细胞(AMC-60)体内和体外生长的影响。用BCG-CWS腹腔注射处理大鼠可诱导同基因腹水瘤消退并增加存活数。在体外细胞生长抑制试验中,腹腔注射BCG-CWS的大鼠的全PEC和贴壁PEC抑制了氚标记胸腺嘧啶核苷摄入纤维肉瘤细胞。随着效应细胞与靶细胞比例增加,这种体外细胞生长抑制作用更显著。此外,当肿瘤细胞与BCG-CWS激活的PEC一起皮下接种时,肿瘤形成明显减少。油刺激的PEC和正常腹腔驻留细胞在体内和体外对肿瘤生长的抑制均无活性。