Pineda Miguel A, Lumb Felicity, Harnett Margaret M, Harnett William
Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow G12 8TA, UK.
Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0NR, UK.
Mol Biochem Parasitol. 2014 Mar-Apr;194(1-2):1-8. doi: 10.1016/j.molbiopara.2014.03.003. Epub 2014 Mar 23.
Filarial nematodes cause long-term infections in hundreds of millions of people. A significant proportion of those affected develop a number of debilitating health problems but, remarkably, such infections are often unnoticed for many years. It is well known that parasitic worms modulate, yet do not completely inhibit, host immunological pathways, promoting their survival by limiting effective immune mechanisms. Such immunoregulation largely depends on molecules released by the worms, termed excretory-secretory products (ES). One of these products is the molecule ES-62, which is actively secreted by the rodent filarial nematode Acanthocheilonema viteae. ES-62 has been shown to exert anti-inflammatory actions thorough its phosphorylcholine (PC)-containing moiety on a variety of cells of the immune system, affecting intracellular signalling pathways associated with antigen receptor- and TLR-dependent responses. We summarise here how ES-62 modulates key signal transduction elements and how such immunomodulation confers protection to mice subjected to certain experimental models of inflammatory disease. Finally, we discuss recent results showing that it is possible to synthetise small molecule analogues (SMAs) that mimic the anti-inflammatory properties of ES-62, opening an exciting new drug development field in translational medicine.
丝虫线虫在数亿人身上引发长期感染。很大一部分感染者会出现一些使人衰弱的健康问题,但值得注意的是,这些感染往往多年都未被察觉。众所周知,寄生虫会调节但不会完全抑制宿主的免疫途径,通过限制有效的免疫机制来促进自身存活。这种免疫调节很大程度上依赖于蠕虫释放的分子,即排泄分泌产物(ES)。其中一种产物是ES - 62分子,它由啮齿类丝虫线虫棘唇线虫(Acanthocheilonema viteae)主动分泌。已表明ES - 62通过其含磷酰胆碱(PC)的部分对免疫系统的多种细胞发挥抗炎作用,影响与抗原受体和Toll样受体(TLR)依赖性反应相关的细胞内信号通路。我们在此总结ES - 62如何调节关键信号转导元件,以及这种免疫调节如何为患有某些炎症性疾病实验模型的小鼠提供保护。最后,我们讨论了最近的研究结果,这些结果表明有可能合成模拟ES - 62抗炎特性的小分子类似物(SMA),从而在转化医学领域开启了一个令人兴奋的新药研发领域。