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用于靶向疫苗递送的甘露糖基化脂质体。

Mannosylated liposomes for targeted vaccines delivery.

作者信息

Vyas Suresh Prasad, Goyal Amit K, Khatri Kapil

机构信息

Department of Pharmaceutical Sciences, Drug Delivery Research Laboratory, Sagar, India.

出版信息

Methods Mol Biol. 2010;605:177-88. doi: 10.1007/978-1-60327-360-2_12.


DOI:10.1007/978-1-60327-360-2_12
PMID:20072881
Abstract

Mannosylated liposomes appear to be a promising and potential carrier system for delivery of proteins, peptides, or nucleic acids. The present chapter describes novel mannosylated liposomes, which increase the intracellular targeting of immunogen to dendritic cells and macrophages possessing the specific receptors. The liposomes used in the present investigation were prepared by hand-shaken method and characterized for size, shape, surface charge, encapsulation efficiency, ligand binding, and specificity and uptake studies. The immune-stimulating activity of the liposomes was studied by measuring antigen-specific antibody titer following subcutaneous administration of different liposomal formulations in BALB/c mice. It was found that O-palmitoyl mannan (OPM)-coated liposomes showed better uptake efficiency. In vivo studies revealed that the OPM-coated liposomes exhibited significant higher serum antibody response and stronger TH1/TH2-based cellular responses. In conclusion, novel vesicular constructs are useful nanosized carriers having superior surface characteristics--for active interaction with the antigen-presenting cells and subsequent processing and presentation of antigen.

摘要

甘露糖基化脂质体似乎是一种用于递送蛋白质、肽或核酸的有前景且具潜力的载体系统。本章描述了新型甘露糖基化脂质体,其可增强免疫原对具有特定受体的树突状细胞和巨噬细胞的细胞内靶向作用。本研究中使用的脂质体通过手摇法制备,并对其大小、形状、表面电荷、包封效率、配体结合以及特异性和摄取研究进行了表征。通过在BALB/c小鼠皮下给予不同脂质体制剂后测量抗原特异性抗体滴度,研究了脂质体的免疫刺激活性。发现O-棕榈酰甘露聚糖(OPM)包被的脂质体表现出更好的摄取效率。体内研究表明,OPM包被的脂质体表现出显著更高的血清抗体反应和更强的基于TH1/TH2的细胞反应。总之,新型囊泡构建体是有用的纳米级载体,具有优异的表面特性,可与抗原呈递细胞进行活性相互作用,并随后对抗原进行加工和呈递。

相似文献

[1]
Mannosylated liposomes for targeted vaccines delivery.

Methods Mol Biol. 2010

[2]
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[3]
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[4]
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[7]
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[8]
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[10]
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Carbohydr Polym. 2018-11-29

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[3]
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[4]
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