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MPG-based nanoparticle: An efficient delivery system for enhancing the potency of DNA vaccine expressing HPV16E7

机译:基于MPG的纳米颗粒:一种有效的递送系统,可增强表达HPV16E7的DNA疫苗的效力

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DNA vaccines against human papillomavirus (HPV) type 16 have not been successful in clinical trials, due to the lack of an appropriate delivery system. In this study, a peptide-based gene delivery system, MPG, which forms stable non-covalent nanoparticles with nucleic acids, was used for in vitro and in vivo delivery of HPV16 E7 DNA as a model antigen. The results demonstrated that at Nitrogen/Phosphate (N/P) ratio over 10:1, this peptide can effectively condense plasmid DNA into stable nanoparticles with an average size of 180-210 nm and a positive surface charge. The transfection efficiency of MPG-based nanoparticles was shown to be comparable with Polyethyleneimine (PEI). The efficient protein expression detected by western blotting and flow cytometry supports the potential of MPG-based nanoparticles as a potent delivery system in DNA vaccine formulations. Immunization with MPG/E7DNA nanoparticles at an N/P ratio of 10:1 induced a stronger Th1 cellular immune response with a predominant interferon-gamma (IFN-gamma) profile than those induced by E7DNA alone in a murine tumor model. These findings suggest that MPG peptide as a novel gene delivery system could have promising applications in improving HPV therapeutic vaccines. (C) 2015 Elsevier Ltd. All rights reserved.
机译:由于缺乏合适的递送系统,抗16型人乳头瘤病毒(HPV)的DNA疫苗尚未在临床试验中获得成功。在这项研究中,基于多肽的基因传递系统MPG与核酸形成稳定的非共价纳米粒子,被用于体外和体内HPV16 E7 DNA作为模型抗原的传递。结果表明,在氮/磷(N / P)比超过10:1的情况下,该肽可以有效地将质粒DNA浓缩为平均大小为180-210 nm且表面带正电荷的稳定纳米颗粒。显示基于MPG的纳米颗粒的转染效率与聚乙烯亚胺(PEI)相当。通过蛋白质印迹和流式细胞术检测到的有效蛋白质表达支持了基于MPG的纳米颗粒作为DNA疫苗制剂中有效的递送系统的潜力。在鼠肿瘤模型中,以N / P比为10:1的MPG / E7DNA纳米颗粒进行免疫诱导的Th1细胞免疫应答更强,主要是干扰素-γ(IFN-γ)谱。这些发现表明,MPG肽作为一种新型的基因传递系统在改善HPV治疗性疫苗方面可能具有广阔的应用前景。 (C)2015 Elsevier Ltd.保留所有权利。

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