Yamaue H, Tanimura H, Tsunoda T, Iwahashi M, Tani M, Tamai M, Noguchi K, Hotta T, Arii K
Department of Gastroenterological Surgery, Wakayama Medical College, Japan.
Biotherapy. 1992;5(1):83-93. doi: 10.1007/BF02194788.
We investigated whether tumor cell lysis by LAK cells was augmented by treatment with OK432 in vitro. NK and LAK activity against K562 cells was not enhanced by their treatment with OK432. In contrast, the susceptibility of OK432-treated Daudi and KATO-III cells to lysis by LAK cells was enhanced. Succinate dehydrogenase activity and RNA synthesis were impaired in Daudi and KATO-III cells by treatment with OK432, and moreover the expression of HLA Class I antigen and beta 2-microglobulin was inhibited in OK432-treated KATO-III cells. Thus, it is suggested that the enhancement of the susceptibility of OK432-treated tumor cells with regard to succinate dehydrogenase activity, RNA synthesis, and HLA Class I antigen expression.
我们研究了在体外经OK432处理后,LAK细胞对肿瘤细胞的裂解作用是否增强。用OK432处理NK细胞和LAK细胞后,其对K562细胞的活性并未增强。相反,经OK432处理的Daudi细胞和KATO-III细胞对LAK细胞裂解的敏感性增强。用OK432处理Daudi细胞和KATO-III细胞后,琥珀酸脱氢酶活性和RNA合成受到损害,此外,经OK432处理的KATO-III细胞中HLA I类抗原和β2-微球蛋白的表达受到抑制。因此,提示经OK432处理的肿瘤细胞在琥珀酸脱氢酶活性、RNA合成和HLA I类抗原表达方面的敏感性增强。