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靶向猪免疫系统——21世纪的颗粒疫苗

Targeting the porcine immune system--particulate vaccines in the 21st century.

作者信息

McCullough Kenneth C, Summerfield Artur

机构信息

Institute of Virology and Immunoprophylaxis, Sensemattstrasse 293, CH-3147 Mittelhäusern, Switzerland.

出版信息

Dev Comp Immunol. 2009 Mar;33(3):394-409. doi: 10.1016/j.dci.2008.07.015. Epub 2008 Sep 2.

DOI:10.1016/j.dci.2008.07.015
PMID:18771683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7103233/
Abstract

During the last decade, the propagation of immunological knowledge describing the critical role of dendritic cells (DC) in the induction of efficacious immune responses has promoted research and development of vaccines systematically targeting DC. Based on the promise for the rational design of vaccine platforms, the current review will provide an update on particle-based vaccines of both viral and synthetic origin, giving examples of recombinant virus carriers such as adenoviruses and biodegradable particulate carriers. The viral carriers carry pathogen-associated molecular patterns (PAMP), used by the original virus for targeting DC, and are particularly efficient and versatile gene delivery vectors. Efforts in the field of synthetic vaccine carriers are focussing on decorating the particle surface with ligands for DC receptors such as heparan sulphate glycosaminoglycan structures, integrins, Siglecs, galectins, C-type lectins and toll-like receptors. The emphasis of this review will be placed on targeting the porcine immune system, but reference will be made to advances with murine and human vaccine delivery systems where information on DC targeting is available.

摘要

在过去十年中,有关树突状细胞(DC)在诱导有效免疫反应中关键作用的免疫学知识传播,推动了系统性靶向DC的疫苗研发。基于合理设计疫苗平台的前景,本综述将更新病毒来源和合成来源的基于颗粒的疫苗,举例说明重组病毒载体如腺病毒和可生物降解颗粒载体。病毒载体携带原始病毒用于靶向DC的病原体相关分子模式(PAMP),是特别高效且通用的基因递送载体。合成疫苗载体领域的工作重点是用DC受体的配体修饰颗粒表面,如硫酸乙酰肝素糖胺聚糖结构、整合素、唾液酸结合凝集素、半乳糖凝集素、C型凝集素和Toll样受体。本综述将重点关注靶向猪免疫系统,但也会提及在小鼠和人类疫苗递送系统方面取得的进展,这些系统有关于DC靶向的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2a/7103233/5d983719b160/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2a/7103233/fe47b5fb3f3a/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2a/7103233/5d983719b160/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2a/7103233/fe47b5fb3f3a/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2a/7103233/5d983719b160/gr2_lrg.jpg

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本文引用的文献

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Memory T cell proliferative responses and IFN-γ productivity sustain long-lasting efficacy of a Cap-based PCV2 vaccine upon PCV2 natural infection and associated disease.在自然感染 PCV2 及其相关疾病后,基于 Cap 的 PCV2 疫苗能够持续诱导记忆 T 细胞增殖反应和 IFN-γ 产生,从而维持其长期疗效。
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