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Microencapsulated plasmids expressing Gn and Gc glycoproteins of Rift Valley Fever virus enhance humoral immune response in mice

机译:表达GN和Rift Valley Fever病毒的GN和GC糖蛋白的微胶囊化质粒增强了小鼠中的体液免疫应答

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Objectives The aim of the current study was to develop biodegradable alginate (ALG)/poly-l-lysine (PLL) microcapsules (MC) with entrapped plasmids expressing Gn and Gc glycoproteins of Rift Valley Fever virus (RVFV) and to evaluate the humoral immune response in mice. Results Expressing phRVF/Gn and phRVF/Gc plasmids which encode full-sized Gn and Gc glycoproteins and contain signal fusion protein F sequences of human parainfluenza (HPIV-1) were constructed. To protect the plasmids from cleavage by extracellular nucleases, they were entrapped into multilayer ALG/PLL microcapsules by layer-by-layer technique. To study the efficacy of humoral immune response, both native and microencapsulated plasmids were injected intramuscular into BALB/c mice. The humoral response in the mice immunized with free plasmids was characterized by virus-neutralizing antibody induction (with titres 1:4 to 1:8), while the injection of microencapsulated plasmids allowed to increase the titre level (from 1:16 to 1:32). Conclusion The plasmids microencapsulated in biodegradable MC could be promising for development of DNA vaccines against RVFV.
机译:目前研究目前的目的是开发可生物降解的藻酸盐(藻)/聚-L-赖氨酸(PLL)微胶囊(MC),其表达Rift Valley Fever病毒(RVFV)的GN和GC糖蛋白的捕获质粒并评估体液免疫小鼠的反应。构建了表达PHRVF / GN和PHRVF / GC质粒的结果,构建了编码全尺寸GN和GC糖蛋白的PHRVF / GC质粒,并含有人对血管胰蛋白酶(HPIV-1)的信号融合蛋白F序列。通过细胞外核酸酶保护从裂解中的质粒,通过层逐层技术捕获到多层藻/ PLL微胶囊中。为了研究体液免疫应答的功效,将天然和微囊化质粒肌肉内注射到BALB / C小鼠中。用游离质粒免疫的小鼠中的液体反应的特征在于病毒 - 中和抗体诱导(用滴度1:4至1:8),同时注射微胶囊化质粒,使滴度水平增加(1:16至1: 32)。结论生物降解MC中微胶囊化的质粒可能是对RVFV的DNA疫苗的开发。

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