DNA-encapsulated magnesium phosphate nanoparticles elicit both humoral and cellular immune responses in mice

Gajadhar Bhakta , Victor Nurcombe , Amarnath Maitra , Anju Shrivastava
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引用次数: 15

Abstract

The efficacy of pEGFP (plasmid expressing enhanced green fluorescent protein)-encapsulated PEGylated (meaning polyethylene glycol coated) magnesium phosphate nanoparticles (referred to as MgPi-pEGFP nanoparticles) for the induction of immune responses was investigated in a mouse model. MgPi-pEGFP nanoparticles induced enhanced serum antibody and antigen-specific T-lymphocyte responses, as well as increased IFN-γ and IL-12 levels compared to naked pEGFP when administered via intravenous, intraperitoneal or intramuscular routes. A significant macrophage response, both in size and activity, was also observed when mice were immunized with the nanoparticle formulation. The response was highly specific for the antigen, as the increase in interaction between macrophages and lymphocytes as well as lymphocyte proliferation took place only when they were re-stimulated with recombinant green fluorescence protein (rGFP). Thus the nanoparticle formulation elicited both humoral as well as cellular responses. Cytokine profiling revealed the induction of Th-1 type responses. The results suggest DNA-encapsulated magnesium phosphate (MgPi) nanoparticles may constitute a safer, more stable and cost-efficient DNA vaccine formulation.

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dna包裹的磷酸镁纳米颗粒在小鼠体内引起体液和细胞免疫反应
在小鼠模型中研究了pEGFP(表达增强型绿色荧光蛋白的质粒)封装聚乙二醇化(聚乙二醇包被)磷酸镁纳米颗粒(简称MgPi-pEGFP纳米颗粒)诱导免疫反应的功效。与裸pEGFP相比,MgPi-pEGFP纳米颗粒通过静脉注射、腹腔注射或肌肉注射可诱导血清抗体和抗原特异性t淋巴细胞反应增强,并增加IFN-γ和IL-12水平。当用纳米颗粒配方免疫小鼠时,也观察到巨噬细胞在大小和活性上的显著反应。这种反应对抗原具有高度特异性,因为巨噬细胞与淋巴细胞相互作用的增加以及淋巴细胞的增殖只有在重组绿色荧光蛋白(rGFP)再次刺激时才会发生。因此,纳米颗粒制剂引起了体液和细胞反应。细胞因子谱显示诱导Th-1型反应。结果表明,DNA封装的磷酸镁(MgPi)纳米颗粒可能构成一种更安全、更稳定和更具成本效益的DNA疫苗制剂。
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