Lotzová E, Savary C A, Freedman R S, Bowen J M
Cancer Immunol Immunother. 1984;17(2):124-9. doi: 10.1007/BF00200048.
We have demonstrated that cancer patients with ovarian carcinoma display deficient peripheral blood NK-cell cytotoxic potential against the K-562 target cell line. Furthermore, no NK-cell activity against the same tumor was detected in ascitic fluids of these patients. The inferior peripheral blood NK-cell cytotoxicity of ovarian carcinoma patients was significantly augmented after ID inoculation with virus-modified tumor cell extract. Similarly, NK-cell activity in the ascitic fluids was dramatically increased after IP in vivo therapy with the same tumor extract preparation. Interestingly, in some of the cancer patients the augmentation of NK-cell activity in ascitic fluids after IP injection of virus-modified tumor cells extract was associated with a clinical response of the patients, as demonstrated by regression of ascitic tumors. These studies indicate, first, that virus-modified tumor extract displays immunopotentiating activity, as reflected by its marked NK cell-augmenting potential, and secondly, that regional activation of NK cells could underlie the mechanism of regression of ascitic tumors.
我们已经证明,患有卵巢癌的癌症患者对K-562靶细胞系表现出外周血NK细胞细胞毒性潜力不足。此外,在这些患者的腹水中未检测到针对同一肿瘤的NK细胞活性。用病毒修饰的肿瘤细胞提取物进行ID接种后,卵巢癌患者外周血NK细胞细胞毒性低下显著增强。同样,用相同的肿瘤提取物制剂进行IP体内治疗后,腹水中的NK细胞活性显著增加。有趣的是,在一些癌症患者中,IP注射病毒修饰的肿瘤细胞提取物后腹水中NK细胞活性的增强与患者的临床反应相关,腹水肿瘤消退证明了这一点。这些研究表明,首先,病毒修饰的肿瘤提取物表现出免疫增强活性,这通过其显著的NK细胞增强潜力得以体现;其次,NK细胞的局部激活可能是腹水肿瘤消退机制的基础。