Kawai K, Sasaki T, Saijo-Kurita K, Akaza H, Koiso K, Ohno T
RIKEN Cell Bank, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.
Cancer Immunol Immunother. 1992;35(4):225-9. doi: 10.1007/BF01789327.
The effect of pretreatment with antitumor drugs on lymphokine-activated killer (LAK) cell cytotoxic activity, determined by lactate-dehydrogenase(LDH)-release assay, was investigated. LAK cells were induced by incubating peripheral blood lymphocytes of healthy donors in medium containing interleukin-2 (IL-2) and monoclonal anti-CD3 antibody for 6-7 days. A human lung squamous carcinoma cell line, SQ-5, was used as an adherent target. After 24 h exposure of the target cells to cisplatin, doxorubicin, or mitomycin C, the drugs were washed off and LAK cells were added at an E/T ratio of 5. During further incubation for 48 h, LDH release from cisplatin- or doxorubicin-pretreated target cells was markedly higher than that from non-pretreated target cells. The combination of cisplatin and LAK cells has an additive cytotoxic effect and that of mitomycin C and LAK cells does not; there may also be an additive effect late in the toxicity mechanism between doxorubicin and LAK cells.
通过乳酸脱氢酶(LDH)释放试验,研究了抗肿瘤药物预处理对淋巴因子激活的杀伤(LAK)细胞细胞毒性活性的影响。将健康供体的外周血淋巴细胞在含白细胞介素-2(IL-2)和单克隆抗CD3抗体的培养基中孵育6 - 7天来诱导LAK细胞。使用人肺鳞癌细胞系SQ - 5作为贴壁靶细胞。在靶细胞暴露于顺铂、阿霉素或丝裂霉素C 24小时后,洗去药物,并以5的效靶比加入LAK细胞。在进一步孵育48小时期间,顺铂或阿霉素预处理的靶细胞的LDH释放明显高于未预处理的靶细胞。顺铂和LAK细胞联合具有相加的细胞毒性作用,而丝裂霉素C和LAK细胞联合则没有;阿霉素和LAK细胞之间在毒性机制后期可能也存在相加作用。