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利用受体生物学实现可生物降解微粒的口服疫苗接种。

Exploiting receptor biology for oral vaccination with biodegradable particulates.

作者信息

Foster Neil, Hirst Barry H

机构信息

School of Dental Sciences, University of Newcastle upon Tyne, Medical School, Newcastle upon Tyne NE2 4HH, UK.

出版信息

Adv Drug Deliv Rev. 2005 Jan 10;57(3):431-50. doi: 10.1016/j.addr.2004.09.009.

Abstract

The effective delivery of antigens via the oral route is an extremely desirable goal. Mucosal delivery of antigens stimulates mucosal and systemic immunity without affecting maternal antibodies and reduces the need for sterile needles or trained personnel. To date, there are very few commercially available oral vaccines and despite numerous reports in the scientific literature to show the success of biodegradable antigen carriers, none of these have achieved commercial status. Nevertheless, many studies have shown the great potential of biodegradable antigen carriers for oral vaccination in preclinical studies, but a more rational approach may be to specifically target antigen-loaded biodegradable microspheres to cells in the mucosal immune system which transport and process antigens for T cell recognition. Modern cell and molecular biology techniques have unearthed a wealth of information regarding important receptors involved in the capture of luminal antigens by microfold or membranous (M) cells and receptors on dendritic cells (DCs) which may allow future targeting of antigens to specific DC phenotypes, thus directing the immune response appropriately. In this review, we consider the use of currently available biodegradable antigen carriers and speculate on how these may be improved to more efficiently target mucosal effector sites.

摘要

通过口服途径有效递送抗原是一个非常理想的目标。抗原的黏膜递送可刺激黏膜和全身免疫,同时不影响母体抗体,还减少了对无菌针头或专业人员的需求。迄今为止,市面上的口服疫苗非常少,尽管科学文献中有大量报道表明可生物降解抗原载体取得了成功,但这些都尚未获得商业地位。然而,许多研究已显示可生物降解抗原载体在临床前研究中用于口服疫苗接种具有巨大潜力,但更合理的方法可能是将负载抗原的可生物降解微球特异性靶向黏膜免疫系统中运输和处理抗原以供T细胞识别的细胞。现代细胞和分子生物学技术已揭示了大量有关微褶或膜性(M)细胞捕获腔内抗原所涉及的重要受体以及树突状细胞(DC)上的受体的信息,这可能使未来能够将抗原靶向特定的DC表型,从而适当地引导免疫反应。在这篇综述中,我们考虑了目前可用的可生物降解抗原载体的用途,并推测如何改进这些载体以更有效地靶向黏膜效应部位。

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