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作 者:陈功[1,2] 黄强 兰青[1,2] 周丽英 楼美清[1,2] 沈茜 王文仲[1,2] 周晓平
机构地区:[1]苏州医学院附二院脑外科 [2]长海医院神经外科及免疫实验室
出 处:《中华神经外科杂志》1998年第3期168-171,共4页Chinese Journal of Neurosurgery
摘 要:目的:探索提高胶质瘤治疗效果的新方法。方法:以化学偶联制备抗CD3-抗胶质瘤双特异性抗体,以3H掺入法测定其与IL-2协同增强LAK细胞对胶质瘤的细胞毒性,以CD3单抗、胶质瘤单抗、二种单抗混和物及RPMI1640作对照。结果:双特异抗体与单抗相比,能显著提高LAK细胞对胶质瘤细胞的杀伤作用;双抗加入IL-2后,LAK细胞毒性得到显著的提高,IL-2也能增强抗CD3单抗和SZ39单抗的细胞毒性;同时发现,来源于恶性胶质瘤患者的LAK细胞毒性,在加入单抗、双抗和IL-2后,其细胞毒性与正常人相比,仍有显著性差异。Objective: To investigate a new method for improving the therapeutic effect on glioma. Method: The antiCD3×antiglioma bispecific antibody (BIAB) was built by chemical conjugating method. Cytotoxicity of LAK cells against glioma cells enhanced by the BIAB and IL2 was examined with3H incorporation method, comparing with control groups: CD3 antibody, antiglioma antibody SZ39, mixture of the two antibodies, RPMI 1640. Results: Cytotoxicity of LAK cells against glioma cells could be markedly enhanced by BIAB compared with antiCD3 and SZ39 monoclonal antibody (P<001 or P<005). When LAK cells incubating with IL2, its cytotoxicity enhanced by BIAB was more high (P<005). Also, we found that cytotoxicty of LAK cells from patients with malignant glioma was lower than that from normal individuals when incubating with antiCD3 and SZ39 monoclonal antibody, BIAB or IL2(P<005,or P<001). Conclusion: AntiCD3×anti glioma BIAB could markedly enhance the cytotoxicity of LAK cells against glioma.
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