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首页> 外文期刊>ACS applied materials & interfaces >In Vivo Imaging Tracking and Immune Responses to Nanovaccines Involving Combined Antigen Nanoparticles with a Programmed Delivery
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In Vivo Imaging Tracking and Immune Responses to Nanovaccines Involving Combined Antigen Nanoparticles with a Programmed Delivery

机译:在涉及组合抗原纳米粒子的纳米杆菌具有编程的抗原纳米粒子的体内成像跟踪和免疫应答

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Combined nanovaccine can generate robust and persistent antigen-specific immune responses. A combined nanovaccine was developed based on antigen-loaded genipin-cross-linked-polyethyleneimine-antigen nanoparticles and in vivo multispectral fluorescence imaging tracked the antigen delivery of combined nanovaccine. The inner layer antigen nanoparticles carried abundant antigens by self-cross-linking for persistent immune response, whereas the outer antigen on the surface of antigen nanoparticles provided the initial antigen exposure. The delivery of combined nanovaccine was tracked dynamically and objectively by the separation of inner genipin cross-linked antigen nanoparticle and the outer fluorescent antigen. The immune responses of the combined nanovaccine were evaluated including antigen-specific CD4(+) and CD8(+) T-cell responses, IgG antibody level, immunological memory, and CD8(+) cytotoxic T lymphocyte responses. The results indicated that the inner and outer antigens of combined vaccine can be tracked in real time with a programmed delivery by the dual fluorescence imaging. The programmed delivery of the inner and outer antigens induced strong immune responses with a combination of a quick delivery and a persistent delivery. With adequate antigen exposure, the dendritic cells were effectively activated and matured, and following T cells were further activated for immune response. Compared with a single nanoparticle formulation, the combined nanovaccine exactly elicited a stronger antigen-specific immune response.
机译:组合的纳米宫可以产生稳健和持续的抗原特异性免疫反应。基于抗原加载的Genipin-交联 - 聚乙烯 - 抗原纳米颗粒和体内多光谱荧光成像进行了组合的纳米乙胺,跟踪纳米虫组合的抗原输送。内层抗原纳米颗粒通过自交联以持续免疫应答而携带丰富的抗原,而抗原纳米颗粒表面上的外抗原提供了初始抗原暴露。通过分离内因交联抗原纳米粒子和外荧光抗原的分离动态地和客观地跟踪组合的纳米宫颈递送。评估组合纳米杆菌的免疫应答,包括抗原特异性CD4(+)和CD8(+)T细胞应答,IgG抗体水平,免疫记忆和CD8(+)细胞毒性T淋巴细胞反应。结果表明,组合疫苗的内抗原可以实时跟踪,通过双荧光成像进行编程递送。内部和外抗原的编程递送诱导强烈的免疫反应,其组合快速递送和持续递送。通过足够的抗原暴露,树枝状细胞被有效地活化和成熟,并且在T细胞中进一步激活免疫应答。与单一纳米颗粒制剂相比,组合的纳米宫恰好引起了更强的抗原特异性免疫应答。

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