氢氧化铝纳米颗粒对登革热亚单位疫苗佐剂的效价研究

S. Pambudi, E. Mardliyati, S. Rahmani, D. Setyawati, T. Widayanti, A. Gill, A. Sulfianti, Whinie Lestari
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摘要

氢氧化铝在疫苗开发中作为佐剂的效力被认为取决于它的颗粒大小。在之前的研究中,我们已经成功制备了两种大小的颗粒,微型和纳米氢氧化铝凝胶(明矾)佐剂。这些颗粒作为候选佐剂的效力需要进行表征。在这项研究中,我们用纯化的DENV3前膜包膜(prM-E)重组蛋白配制佐剂,并评估了对小鼠巨噬细胞RAW 264.7细胞一氧化氮水平的诱导作用。采用沉淀-均质法制备明矾佐剂,搅拌速率为11000xg。利用毕赤酵母X-33进行生物反应器发酵,提取重组蛋白prM-E。重组蛋白的纯化采用阴离子交换层析和大小排斥层析。纯化后的prM-E重组蛋白在70 -1k Da左右呈单条带,浓度为105 mg mL。含prM-E蛋白的复合纳米明矾显著(p<0.05)诱导一氧化氮水平升高。纳米明矾佐剂、重组蛋白和细胞免疫应答的分子机制有待进一步分析。
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The Potency of Aluminum Hydroxide Nanoparticles for Dengue Subunit Vaccine Adjuvant
The potency of aluminum hydroxide as an adjuvant in vaccine development is considered to depend on its particle size. In previous studies, we have successfully prepared two size particle, micro, and nano, aluminum hydroxide gel (alum) adjuvants. The potency of those particles as a candidate of adjuvant is needed to be characterized. In this study, we formulated our adjuvants with purified DENV3 pre Membrane Envelope (prM-E) recombinant protein and evaluated the induction of nitric oxide level in mouse macrophage RAW 264.7 cells. We prepared the alum adjuvant by precipitation-homogenization methods with an agitation rate at 11,000xg. Secreted prM-E recombinant protein was collected from Pichia pastoris X-33 fermentation which produced using bioreactor. Recombinant protein purification was carried out by anion exchange chromatography followed with size exclusion chromatography. The purified prM-E recombinant protein was observed as a single band around 70 -1k Da with a concentration of 105 mg mL . Complex nanoparticles alum with prM-E protein significantly (p<0.05) induced the nitric oxide level. Further analysis should be conducted in order to discover the detail molecular mechanism of nanoparticle alum adjuvant, recombinant protein, and cellular immune response.
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