Fu J Y
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1989 Dec;11(6):446-8.
Previous studies showed that the depressed NK cell activity in tumor-bearing mice was not due to the decrease of NK cell number. The results of this report indicate that the depressed NK cell activity in tumor-bearing mice might be due to an inhibitory factor, which probably was secreted by tumor-cells. We found that sera and peritoneal exudates from S180 or P388 tumor-bearing mice were able to inhibit the normal NK cell activity. Spleen cells incubated with the peritoneal exudate for 24 hours before assay demonstrated significantly depressed NK activity. Treatment of peritoneal exudate with a large number of spleen cells did not alter the inhibitory effect of peritoneal fluid, indicating that the inhibitory factor might not be membrane antigen shedding from the tumor cells, but may be actively secreted by them.
先前的研究表明,荷瘤小鼠自然杀伤(NK)细胞活性降低并非由于NK细胞数量减少。本报告结果表明,荷瘤小鼠NK细胞活性降低可能是由于一种抑制因子,该因子可能由肿瘤细胞分泌。我们发现,来自S180或P388荷瘤小鼠的血清和腹腔渗出液能够抑制正常NK细胞活性。在检测前将脾细胞与腹腔渗出液孵育24小时,结果显示NK活性显著降低。用大量脾细胞处理腹腔渗出液并未改变腹腔液的抑制作用,这表明抑制因子可能不是肿瘤细胞脱落的膜抗原,而是可能由它们主动分泌的。