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通过乳酸脱氢酶释放试验测定抗肿瘤药物和淋巴因子激活的杀伤细胞细胞毒活性在杀伤肿瘤细胞中的相加作用。

Additive effects of antitumor drugs and lymphokine-activated killer cell cytotoxic activity in tumor cell killing determined by lactate-dehydrogenase-release assay.

作者信息

Kawai K, Sasaki T, Saijo-Kurita K, Akaza H, Koiso K, Ohno T

机构信息

RIKEN Cell Bank, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.

出版信息

Cancer Immunol Immunother. 1992;35(4):225-9. doi: 10.1007/BF01789327.

Abstract

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.

摘要

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。

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