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作为免疫调节剂的蠕虫寄生虫分泌产物。

Secretory products of helminth parasites as immunomodulators.

作者信息

Harnett William

机构信息

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral Street, Glasgow G4 0RE, United Kingdom.

出版信息

Mol Biochem Parasitol. 2014 Jul;195(2):130-6. doi: 10.1016/j.molbiopara.2014.03.007. Epub 2014 Apr 3.

DOI:10.1016/j.molbiopara.2014.03.007
PMID:24704440
Abstract

Parasitic helminths release molecules into their environment, which are generally referred to as excretory-secretory products or ES. ES derived from a wide range of nematodes, trematodes and cestodes have been studied during the past 30-40 years, their characterization evolving from simple biochemical procedures such as SDS-PAGE in the early days to sophisticated proteomics in the 21st century. Study has incorporated investigation of ES structure, potential as vaccines, immunodiagnostic utility, functional activities and immunomodulatory properties. Immunomodulation by ES is increasingly the area of most intensive research with a number of defined helminth products extensively analyzed with respect to the nature of their selective effects on cells of the immune system as well as the molecular mechanisms, which underlie these immunomodulatory effects. As a consequence, we are now beginning to learn the identities of the receptors that ES employ and are increasingly acquiring detailed knowledge of the signalling pathways that they interact with and subvert. Such information is contributing to the growing idea that the anti-inflammatory properties of a number of ES products makes them suitable starting points for the development of novel drugs for treating human inflammatory disease.

摘要

寄生性蠕虫会向其生存环境中释放一些分子,这些分子通常被称为排泄分泌产物或ES。在过去的30到40年里,人们对源自多种线虫、吸虫和绦虫的ES进行了研究,其特征从早期简单的生化方法(如SDS-PAGE)发展到21世纪复杂的蛋白质组学。研究内容包括ES的结构、作为疫苗的潜力、免疫诊断用途、功能活性和免疫调节特性。ES的免疫调节作用日益成为研究最为密集的领域,许多已明确的蠕虫产物在对免疫系统细胞的选择性作用性质以及这些免疫调节作用背后的分子机制方面都得到了广泛分析。因此,我们现在开始了解ES所利用的受体身份,并越来越详细地掌握它们与之相互作用和破坏的信号通路。这些信息促使人们越来越认为,许多ES产物的抗炎特性使其成为开发治疗人类炎症性疾病新药的合适起点。

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