Dalton John P, Robinson Mark W, Mulcahy Grace, O'Neill Sandra M, Donnelly Sheila
Institute of Parasitology, McGill University, 21111 Lakeshore Road, St. Anne de Bellevue, Quebec H9X 3V9, Canada.
Vet Parasitol. 2013 Aug 1;195(3-4):272-85. doi: 10.1016/j.vetpar.2013.04.008. Epub 2013 Apr 6.
The liver fluke, Fasciola hepatica, causes fascioliasis in domestic animals (sheep, cattle), a global disease that is also an important infection of humans. As soon as the parasite invades the gut wall its interaction with various host immune cells (e.g. dendritic cells, macrophages and mast cells) is complex. The parasite secretes a myriad of molecules that direct the immune response towards a favourable non-protective Th2-mediate/regulatory environment. These immunomodulatory molecules, such as cathepsin L peptidase (FhCL1), are under development as the first generation of fluke vaccines. However, this peptidase and other molecules, such as peroxiredoxin (FhPrx) and helminth defence molecule (FhHDM-1), exhibit various immunomodulatory properties that could be harnessed to help treat immune-related conditions in humans and animals.
肝吸虫,即肝片吸虫(Fasciola hepatica),可在家畜(绵羊、牛)中引发肝片吸虫病,这种全球性疾病也是人类的一种重要感染源。一旦寄生虫侵入肠壁,它与各种宿主免疫细胞(如树突状细胞、巨噬细胞和肥大细胞)的相互作用就很复杂。寄生虫会分泌大量分子,将免疫反应导向有利的非保护性Th2介导/调节性环境。这些免疫调节分子,如组织蛋白酶L肽酶(FhCL1),正作为第一代吸虫疫苗进行研发。然而,这种肽酶和其他分子,如过氧化物还原酶(FhPrx)和蠕虫防御分子(FhHDM-1),具有多种免疫调节特性,可用于帮助治疗人类和动物的免疫相关疾病。