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Dengue type 2 virus subviral extracellular particles produced by a stably transfected mammalian cell line and their evaluation for a subunit vaccine

机译:稳定转染的哺乳动物细胞系产生的登革热2型病毒亚病毒胞外颗粒及其亚单位疫苗的评估

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摘要

A dengue subunit vaccine candidate was developed using a mammalian cell line continuously expressing subviral extracellular particles (EPs) of the New Guinea C (NGC) strain of dengue type 2 virus. The cell line, designated D cell line, maintained envelope (E) antigen production for at least 10 passages. The EPs contained an E protein biochemically and antigenically equivalent to authentic E produced by NGC-infected Vero cells. Two immunizations of BALB/c mice with purified EPs containing 100 ng or 400 ng of E induced moderate levels of neutralizing antibody and anamnestic neutralizing antibody responses were produced when these animals were challenged with L dengue virus. The yield of E antigen from D cells was comparable to that from NGC-infected Vero cells. When D cells were transfected with the anti-apoptotic bcl-2 gene, the E antigen release increased approximately two-fold. These results indicate that D cell EPs are a promising non-infectious vaccine antigen for dengue.
机译:使用连续表达2型登革热新几内亚C(NGC)株的亚病毒细胞外颗粒(EPs)的哺乳动物细胞系,开发了登革热亚单位疫苗候选物。该细胞系,称为D细胞系,维持至少10代的包膜(E)抗原产生。 EP包含与EGC感染的Vero细胞产生的真实E具有生化和抗原性等同的E蛋白。当这些动物受到L登革热病毒攻击时,用含有100 ng或400 ng E的纯化EP免疫BALB / c小鼠两次,可诱导中等水平的中和抗体反应和记忆中和抗体反应。 D细胞的E抗原产量可与NGC感染的Vero细胞相比。当用抗凋亡的bcl-2基因转染D细胞时,E抗原的释放增加了大约两倍。这些结果表明,D细胞EP是登革热的有希望的非感染性疫苗抗原。

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