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作 者:毕锋[1] 张学庸[1] 牟震先[1] 吴觉平[1] 樊代明[1] 吴开春[1]
机构地区:[1]第四军医大学西京医院消化病研究室,西安710032
出 处:《中国肿瘤生物治疗杂志》1996年第1期42-44,共3页Chinese Journal of Cancer Biotherapy
摘 要:在LAK细胞对胃癌细胞KATOⅢ的杀伤过程中,加入单克隆抗体MGb2能产生明显协同作用。推测此作用的原理是抗体依赖细胞介导的细胞毒性作用(ADCC)。此作用随着制备LAK细胞时白细胞介素2(IL-2)浓度的增加而增高,与LAK活性呈平行关系;制备LAK细胞时,IL-2的诱导时间既影响LAK活性,也影响相应的ADCC作用。The cytotoxicity against gastric cancer cell line KATO Ⅲ of lymphokine activated killer (LAK) cells produced from human peripheral blood mononuclear cells (PBMC) stimulated by interleukin-2 (IL-2) was observed and compared with that of LAK cells together with antigastric cancer monoclonal antibody (McAb) of MGb2. The killing capacity was found to be increased significantly (about 100%, P< 0. 01)when the antigastric McAb MGb2 was added. The ADCC paralleled the LAK activity. When the concentration of IL-2 was 200U/ml, both the LAK activity and ADCC reached their maximum after four days incubation. Our study demonstrated that the combined use of McAb MGb2 and LAK cell may carry a great promise to improve the theapeutic effect for gastric cancer patient.
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