Zhang Jingying, Tang Yongmin, Qian Baiqin, Sheng Hongqiang
Division of Hematology-Oncology, Children's Hospital, School of Medicine, Zhejiang University, Hangzhou, 310003, China.
J Huazhong Univ Sci Technolog Med Sci. 2010 Apr;30(2):240-7. doi: 10.1007/s11596-010-0222-1. Epub 2010 Apr 21.
In this study, norcanthridin (NCTD)-encapsulated liposomes were modified with a novel murine anti-human CD19 monoclonal antibody 2E8 (2E8-NCTD-liposomes) and the targeting efficiency and specific cytotoxicity of 2E8-NCTD-liposomes to CD19(+) leukemia cells were evaluated. BALB/c mice were injected with 2E8 hybridoma cells to obtain 2E8 monoclonal antibody (mAb). NCTD-liposomes were prepared by using film dispersion method. 2E8 mAbs were linked to NCTD-liposomes using post-incorporation technology. Flow cytometry showed that the targeting efficiency of purified 2E8 mAbs on CD19(+) Nalm-6 cells was 99.93%. The purified 2E8 mAbs were conjugated with NCTD-liposomes to prepare 2E8-NCTD-liposomes whose targeting efficiency on CD19(+) Nalm-6 was also 95.82%. The average size of 2E8-NCTD-liposomes was 118.32 nm in diameter. HPLC showed that the encapsulation efficiency of NCTD was 46.51%. When the molar ratio of 2E8/Mal-PEG(2000)-DSPE reached 1:50, we obtained the liposomes with 9 2E8 molecules per liposome. The targeting efficiency of 2E8-NCTD-liposomes on CD19(+) leukemia cells was significantly higher than that on CD19-leukemia cells. Similarly, the targeting efficiency of the immunoliposomes was also higher than that of the NCTD-liposomes on CD19(+) leukemia cells. Those results were consistent with those observed by laser scanning confocal microscopy. 3-(4, 5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay demonstrated that 2E8-NCTD-liposomes specifically killed Nalm-6 cells in a dose- and time-dependent manner. The viability of Nalm-6 cells treated by 2E8-NCTD-liposomes was significantly lower than that of Molt-3 cells and it was also significantly lower than that of Nalm-6 cells treated with the same concentration of NCTD-liposomes or free NCTD. We are led to concluded that 2E8 antigen can serve as a specific targeting molecule of B lineage hematopoietic malignancies for liposome targeting, and 2E8-NCTD-liposomes can be used as a new and effective means for the treatment of B lineage hematopoietic malignancies.
在本研究中,用新型鼠抗人CD19单克隆抗体2E8修饰去甲斑蝥素(NCTD)包裹的脂质体(2E8-NCTD-脂质体),并评估2E8-NCTD-脂质体对CD19(+)白血病细胞的靶向效率和特异性细胞毒性。给BALB/c小鼠注射2E8杂交瘤细胞以获得2E8单克隆抗体(mAb)。采用薄膜分散法制备NCTD-脂质体。使用后掺入技术将2E8 mAb连接到NCTD-脂质体上。流式细胞术显示纯化的2E8 mAb对CD19(+) Nalm-6细胞的靶向效率为99.93%。将纯化的2E8 mAb与NCTD-脂质体偶联以制备2E8-NCTD-脂质体,其对CD19(+) Nalm-6的靶向效率也为95.82%。2E8-NCTD-脂质体的平均直径为118.32 nm。高效液相色谱显示NCTD的包封率为46.51%。当2E8/Mal-PEG(2000)-DSPE的摩尔比达到1:50时,我们获得了每个脂质体含有9个2E8分子的脂质体。2E8-NCTD-脂质体对CD19(+)白血病细胞的靶向效率显著高于对CD19-白血病细胞的靶向效率。同样,免疫脂质体对CD19(+)白血病细胞的靶向效率也高于NCTD-脂质体。这些结果与激光扫描共聚焦显微镜观察到的结果一致。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)试验表明,2E8-NCTD-脂质体以剂量和时间依赖性方式特异性杀死Nalm-6细胞。用2E8-NCTD-脂质体处理的Nalm-6细胞的活力显著低于Molt-3细胞,也显著低于用相同浓度的NCTD-脂质体或游离NCTD处理的Nalm-6细胞。我们得出结论,2E8抗原可作为B系造血恶性肿瘤脂质体靶向的特异性靶向分子,2E8-NCTD-脂质体可作为治疗B系造血恶性肿瘤的一种新的有效手段。