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囊性棘球蚴病中的寄生虫分子与宿主反应

Parasite molecules and host responses in cystic echinococcosis.

作者信息

Díaz A, Casaravilla C, Barrios A A, Ferreira A M

机构信息

Cátedra de Inmunología, Departamento de Biociencias (Facultad de Química) and Instituto de Química Biológica (Facultad de Ciencias), Universidad de la República, Montevideo, Uruguay.

出版信息

Parasite Immunol. 2016 Mar;38(3):193-205. doi: 10.1111/pim.12282.

Abstract

Cystic echinococcosis is the infection by the larvae of cestode parasites belonging to the Echinococcus granulosus sensu lato species complex. Local host responses are strikingly subdued in relation to the size and persistence of these larvae, which develop within mammalian organs as 'hydatid cysts' measuring up to tens of cm in diameter. In a context in which helminth-derived immune-suppressive, as well as Th2-inducing, molecules garner much interest, knowledge on the interactions between E. granulosus molecules and the immune system lags behind. Here, we discuss what is known and what are the open questions on E. granulosus molecules and structures interacting with the innate and adaptive immune systems, potentially or in demonstrated form. We attempt a global biological approach on molecules that have been given consideration primarily as protective (Eg95) or diagnostic antigens (antigen B, antigen 5). We integrate glycobiological information, which traverses the discussions on antigen 5, the mucin-based protective laminated layer and immunologically active preparations from protoscoleces. We also highlight some less well-known molecules that appear as promising candidates to possess immune-regulatory activities. Finally, we point out gaps in the molecular-level knowledge of this infectious agent that hinder our understanding of its immunology.

摘要

囊型包虫病是由细粒棘球绦虫复合种的绦虫寄生虫幼虫感染引起的。与这些在哺乳动物器官内发育成直径可达数十厘米的“包虫囊肿”的幼虫的大小和持久性相比,局部宿主反应明显受到抑制。在蠕虫衍生的免疫抑制分子以及诱导Th2的分子备受关注的背景下,关于细粒棘球绦虫分子与免疫系统之间相互作用的知识却滞后了。在这里,我们讨论了已知的以及关于细粒棘球绦虫分子和结构与先天和适应性免疫系统相互作用的未解决问题,这些相互作用可能以已证实的形式存在。我们尝试对主要被视为保护性(Eg95)或诊断性抗原(抗原B、抗原5)的分子采用全球生物学方法。我们整合了糖生物学信息,这些信息贯穿了关于抗原5、基于粘蛋白的保护性层状膜和原头蚴免疫活性制剂的讨论。我们还强调了一些鲜为人知但似乎有希望具有免疫调节活性 的分子。最后,我们指出了这种感染因子在分子水平知识上的差距,这些差距阻碍了我们对其免疫学的理解。

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