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体外和离体鉴定包被凝集素的结核分枝杆菌抗原微球用于增强口服递送。

In vitro and ex vivo characterization of lectin-labeled Mycobacterium tuberculosis antigen-containing microspheres for enhanced oral delivery.

机构信息

College of Pharmacy, Harding University , Searcy, AR , USA .

出版信息

J Drug Target. 2014 Jan;22(1):34-47. doi: 10.3109/1061186X.2013.833206. Epub 2013 Aug 29.

Abstract

PURPOSE

Oral immunization for mucosal protection against Mycobacterium tuberculosis would be the best option for effective tuberculosis (TB) control. However, this route of vaccine delivery is limited due to the short residence time of the delivery system at the site of absorption. Cytoadhension has made it possible to optimize the targeted delivery of oral vaccine to lymphoid tissues. The purpose of this project was to evaluate the ability of human M-cell specific lectin-labeled microparticles to target the human M-cells of the Peyer's patches.

METHOD

Albumin microspheres containing Mycobacterium tuberculosis cell lysate antigens were coupled with Wheat germ agglutinin and Aleuria aurantia lectins and their ability to bind to M cell models as well as their preferential distribution in the Peyer's patches were investigated.

RESULTS

The study demonstrated an enhanced delivery of targeted polystyrene and BSA/Lysate microspheres to M cells. It was demonstrated that alpha-l-fucose sugar residue might be the target of these lectins.

CONCLUSION

It can be concluded from the study that the lectin-coupled microspheres had better affinity for M-cells and showed preferential binding to the Peyer's patches. This means that the coupling enhanced the targeted delivery of the antigens to the M cells.

摘要

目的

针对结核分枝杆菌(Mycobacterium tuberculosis)的粘膜保护的口服免疫接种将是控制结核病(TB)的最佳选择。然而,由于输送系统在吸收部位的停留时间短,这种疫苗输送途径受到限制。细胞黏附使得优化口服疫苗向淋巴组织的靶向投递成为可能。本项目的目的是评估人 M 细胞特异性凝集素标记的微粒体将疫苗靶向人派尔集合淋巴结(Peyer's patches)的 M 细胞的能力。

方法

载有结核分枝杆菌细胞裂解物抗原的白蛋白微球与麦胚凝集素和美洲商陆凝集素偶联,并研究其与 M 细胞模型的结合能力以及在派尔集合淋巴结中的优先分布情况。

结果

研究表明,靶向聚苯乙烯和 BSA/Lysate 微球对 M 细胞的传递得到了增强。研究表明,α-l-岩藻糖残基可能是这些凝集素的靶标。

结论

从研究中可以得出结论,与凝集素偶联的微球对 M 细胞具有更好的亲和力,并优先结合派尔集合淋巴结。这意味着,偶联增强了抗原对 M 细胞的靶向传递。

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