Lawrence R A, Devaney E
School of Biological Sciences, University of Manchester, Manchester, UK.
Parasite Immunol. 2001 Jul;23(7):353-61. doi: 10.1046/j.1365-3024.2001.00396.x.
Mouse models of Brugia infection have provided much useful quantitative and qualitative information on the immune response elicited by different life cycle stages of filarial worms. Many parallels exist between the immune response in the mouse and the infected human and in this review we highlight areas of topical interest, including the induction of specific cytokine responses and their role in immunomodulation and protective immunity. These studies have reinforced the concept that different life cycle stages of filarial parasites each have their own mechanism of modulating responses so that potentially inflammatory IFN-gamma responses are downregulated. While the precise mechanisms of protective immunity remain to be defined, studies in the mouse have suggested novel pathways, including a possible role for granulocytes.
布鲁氏菌感染的小鼠模型已经提供了许多关于丝虫不同生命周期阶段引发的免疫反应的有用定量和定性信息。小鼠和受感染人类的免疫反应之间存在许多相似之处,在本综述中,我们重点介绍了当前感兴趣的领域,包括特定细胞因子反应的诱导及其在免疫调节和保护性免疫中的作用。这些研究强化了这样一种概念,即丝虫寄生虫的不同生命周期阶段各自具有调节反应的机制,从而使潜在的炎症性干扰素-γ反应下调。虽然保护性免疫的确切机制仍有待确定,但在小鼠身上进行的研究已经提出了新的途径,包括粒细胞可能发挥的作用。