首页> 中文期刊>中华微生物学和免疫学杂志 >鼻咽癌特异性减毒重组疫苗 Lmdd-LMP2 A 的构建及其抑瘤效应的研究

鼻咽癌特异性减毒重组疫苗 Lmdd-LMP2 A 的构建及其抑瘤效应的研究

摘要

Objective To prepare an attenuated Listeria vaccine Lmdd-LMP2A expressing the Ep-stein-Barr virus latent membrane protein 2A ( EBV-LMP2A) and evaluate its specific anti-tumor effects on nasopharyngeal carcinoma.Methods The gene fragment encoding EBV-LMP2A was amplified by PCR analysis and then subcloned into the shuttle vector p1565.PCR restriction enzyme digestion and DNA se-quencing were performed to identify the recombinant shuttle vector p1565-LMP2A.The p1565-LMP2A vector was then transformed into competent strains of the attenuated Listeria monocytogenes ( Lmdd) .The recombi-nant attenuated Listeria vaccine strain Lmdd-LMP2A was verified by Western blot assay.The histological sections of spleen and liver tissues were stained by Haematoxylin and eosin ( H&E) for analysis of inflamma-tion.A tumor-bearing HLA-A2 transgenic mouse model was established by subcutaneous injection of CNE-1/HLA-A2/LMP2A nasopharyngeal carcinoma cell line.The prepared Lmdd-LMP2A vaccine was inoculated into the mice via tail intravenous injection for the evaluation of specific CTL induction and the in vivo anti-tumor effects.Results The shuttle vector p1565-LMP2A and the recombinant attenuated Listeria vaccine strain Lmdd-LMP2A with stable expression of LMP2A protein were successfully constructed.The immunized mice showed mild inflammations with no structural damage and necrosis as indicated by H&E staining.The growth of tumors in tumor-bearing HLA-A2 transgenic mice was significantly inhibited by the immunization of Lmdd-LMP2A vaccine as compared with mice without inoculation.The survival time of mice was prolonged with the immunization of Lmdd-LMP2A vaccine.Conclusion The prepared attenuated Listeria vaccine Lm-dd-LMP2A showed specific anti-tumor effects with the safety advantage, suggesting the possibility of using it for anti-tumor therapy in clinic.%目的:构建含有EB病毒潜伏膜蛋白2A(LMP2A)的减毒单核增生性李斯特菌重组疫苗(Lmdd-LMP2A),并检测其抑瘤效应,旨在为鼻咽癌的免疫治疗提供新的思路及理论依据。方法将EBV-LMP2A基因克隆入李斯特菌穿梭载体p1565中,再将重组穿梭载体p1565-LMP2A电转化至减毒单核增生性李斯特菌株Lmdd感受态细胞中,得到重组疫苗Lmdd-LMP2A。进而对HLA-A2转基因小鼠皮下接种CNE-1/HLA-A2/LMP2A鼻咽癌细胞株,建立皮下荷瘤鼠模型。利用尾静脉注射法接种李斯特菌疫苗免疫荷瘤鼠并检测其特异性CTL诱导情况及抑瘤效应。结果成功构建了重组减毒李斯特菌鼻咽癌疫苗Lmdd-LMP2A,该疫苗高度减毒,安全性较好且稳定表达LMP2A蛋白并诱导特异性T细胞免疫应答。荷瘤鼠抑瘤模型结果表明,与对照组相比,Lmdd-LMP2A能明显的抑制肿瘤生长。并且,Lmdd-LMP2A免疫组也能延长小鼠的荷瘤生存期,均显示了该种重组疫苗的有效抑瘤价值。结论成功构建的减毒重组李斯特菌疫苗Lmdd-LMP2A,可以在确保安全性的同时发挥良好的特异性抗肿瘤效应,对于肿瘤治疗具有潜在的临床意义。

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