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蠕虫诱导的细胞凋亡:一种免疫抑制的沉默策略。

Helminth-induced apoptosis: a silent strategy for immunosuppression.

作者信息

Zakeri Amin

机构信息

Department of Pathobiology,Faculty of Veterinary Medicine,Ferdowsi University of Mashhad,Mashhad,Iran.

出版信息

Parasitology. 2017 Nov;144(13):1663-1676. doi: 10.1017/S0031182017000841. Epub 2017 Jun 29.

DOI:10.1017/S0031182017000841
PMID:28659212
Abstract

During microbial infections, both innate and adaptive immunity are activated. Viruses and bacteria usually induce an acute inflammation in the first setting of infection, which helps the eliciting an effective immune response. In contrast, macroparasites such as helminths are a highly successful group of invaders known to be capable of maintaining a chronic infestation with the minimum instigation. Undoubtedly, generating such an immunoregulatory environment requires the exploitation of various immunosuppressive mechanisms to debilitate host immunity supporting their survival and replication. Several mechanisms have been recognized whereby helminths prolong their infections including an increase of immunoregulatory cells, inhibition of Th1 or Th2 responses, targeting pattern recognition receptors (PRRs) and lowering the immune cells quantity via induction of apoptosis. Apoptosis is a programmed intracellular process involving a series of consecutive downstream signalling event evolved to cell death. It plays a pivotal role in several immunological reactions in particular deletion of autoreactive immune cells. Helminth-triggered apoptosis in immune cells exhausts host immunity, which paves the way for generating a permissive environment and chronic infection. This review provides a compilation of recent investigations discussing the apoptotic mechanisms exploited by different worms and the immunological consequences of immune cell death. Finally, the anti-cancer effects of some worm-derived molecules due to their apoptotic effects are discussed, highlighting as potentially druggable candidates to combat cancer.

摘要

在微生物感染期间,固有免疫和适应性免疫都会被激活。病毒和细菌通常在感染初期引发急性炎症,这有助于引发有效的免疫反应。相比之下,诸如蠕虫等大型寄生虫是一类非常成功的入侵者,已知它们能够以最小的刺激维持慢性感染。毫无疑问,营造这样一种免疫调节环境需要利用各种免疫抑制机制来削弱宿主免疫,以支持它们的生存和繁殖。已经认识到几种机制,通过这些机制蠕虫延长其感染,包括增加免疫调节细胞、抑制Th1或Th2反应、靶向模式识别受体(PRR)以及通过诱导凋亡降低免疫细胞数量。凋亡是一个程序性细胞内过程,涉及一系列连续的下游信号事件,最终导致细胞死亡。它在几种免疫反应中起关键作用,特别是在清除自身反应性免疫细胞方面。蠕虫触发的免疫细胞凋亡耗尽宿主免疫,这为营造一个宽松环境和慢性感染铺平了道路。本综述汇编了近期的研究,讨论了不同蠕虫利用的凋亡机制以及免疫细胞死亡的免疫学后果。最后,讨论了一些蠕虫衍生分子因其凋亡作用而产生的抗癌效果,强调它们作为对抗癌症的潜在可药物化候选物。

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