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出 处:《中华血液学杂志》1998年第5期230-233,共4页Chinese Journal of Hematology
基 金:国家自然科学基金;天津市自然科学基金
摘 要:目的:探讨高度恶性的小鼠T淋巴细胞白血病细胞系L615转导B71基因后激发移植宿主体内的抗肿瘤免疫情况。方法:以逆转录病毒为载体,将B71基因导入小鼠白血病细胞系L615中,获得高表达B71分子的L615B7细胞,作为肿瘤疫苗进行体内移植,观察其免疫保护作用并检测瘤苗体外激活的T细胞杀伤活性、细胞增殖和因子分泌情况。结果:体内移植实验表明B71分子的表达可降低L615细胞在小鼠中的致瘤性,明显延长其生存时间。用B7瘤苗预先免疫小鼠,对随后的瘤细胞攻击有明显的免疫保护作用。B7瘤苗体外活化的T细胞对同种细胞有特异性杀伤活性,并可刺激L615B7的增殖。结论:B71基因的导入并有效表达可增强肿瘤细胞免疫原性,激活T细胞。Objective: To assess the potential of B71 vaccine in inducing immunity to leukemic cells. Methods: B71 gene was introduced into L615 cells and then the positive clone (L615B7) highly expressing B71 was selected. Tumorigenic and immunoprotective activities of L615B7 cells were studied in vivo. T cell functions of cytotoxicity , proliferation and growth factor secretion were detected in vitro.Results: Syngeneic 615 mice receiving L615B7 cells survived longer than control. After being immunized with L615B7,the mice gained remarkable immunoprotection against the following challenge of wildtype L615 cells, and in some mice could survive over a long duration. In vitro, the B7activated effector cells exhibited a specific cytotoxicity to L615 and L615B7 cells,and an enhanced proliferation in response to L615B7. Conclusion:B7 vaccine could improve the immunogenicity of tumor cells , activate T cells and enhance in vivo the antitumor immunity.
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