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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >DNA tattoo vaccination: Effect on plasmid purity and transfection efficiency of different topoisoforms
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DNA tattoo vaccination: Effect on plasmid purity and transfection efficiency of different topoisoforms

机译:DNA纹身疫苗接种:对不同拓扑异构体的质粒纯度和转染效率的影响

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摘要

Recently, DNA tattooing was introduced as novel intradermal administration technique for plasmid DNA (pDNA) vaccines. The aim of this study was to determine if tattooing affects the integrity of pDNA (reduction in supercoiled (SC) content) and whether a change in pDNA topology would affect antigen expression and immune response. We show that 1.) in vitro tattooing of pDNA solutions results in minor damage to pDNA (<= 3% SC pDNA reduction) and only open circular (OC) pDNA formation, 2.) antigen expression and T-cell responses upon tattoo administration of SC and OC pDNA are equal in a murine model, 3.) SC pDNA gives a significantly higher antigen expression than OC and linear pDNA in ex vivo human skin, 4.) pDNA topology does not influence antigen expression when formulated as PEGylated polyplexes. We conclude that a 3% reduction in SC purity most likely will have little or no effect on clinical antigen expression and T-cell responses. For intradermal tattoo administration the ex vivo skin model might be more suitable than the standard murine model for distinguishing subtle alterations in antigen expression of clinical pDNA formulations. The results from this study enable justification of release and shelf-life specifications of pDNA products applied by this specific route of administration, as requested by the regulatory authorities (>= 80% SC).
机译:最近,DNA纹身被引入作为质粒DNA(pDNA)疫苗的新型皮内给药技术。这项研究的目的是确定纹身是否会影响pDNA的完整性(超螺旋(SC)含量的减少)以及pDNA拓扑结构的变化是否会影响抗原表达和免疫反应。我们显示1.)pDNA溶液的体外纹身会导致对pDNA的轻微损坏(<= 3%SC pDNA减少),并且仅形成开放的环状(OC)pDNA,2.)纹身施用后抗原表达和T细胞反应在鼠模型中,SC和OC pDNA的比例相等。3.)SC pDNA在离体人体皮肤中的抗原表达比OC和线性pDNA显着高。4.)当配制成PEG化多聚体时,pDNA拓扑结构不影响抗原表达。我们得出结论,SC纯度降低3%很可能对临床抗原表达和T细胞反应几乎没有影响。对于皮内纹身给药,离体皮肤模型可能比标准鼠模型更适合于区分临床pDNA制剂抗原表达中的细微变化。根据监管机构的要求(> = 80%SC),该研究的结果可证明通过这种特定的给药途径应用的pDNA产品的释放和保存期限规格合理。

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