The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, affiliated to Sackler Faculty of Medicine, Tel Aviv, Israel.
The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, affiliated to Sackler Faculty of Medicine, Tel Aviv, Israel; Department of Gastroenterology, Sheba Medical Center, Tel Hashomer, affiliated to Sackler Faculty of Medicine, Tel Aviv, Israel.
Autoimmun Rev. 2015 Feb;14(2):98-104. doi: 10.1016/j.autrev.2014.10.004. Epub 2014 Oct 16.
The incidence of autoimmune diseases has risen throughout the last half a century, mostly in the industrialized world. Helminths and their derivatives were found to have a protective role in autoimmunity and inflammatory conditions, as they manipulate the immune network, attenuating the host's cellular and humoral responses. Indeed, various helminth species used in several human and animal models were shown to limit inflammatory activity in a variety of diseases including inflammatory bowel disease, multiple sclerosis, type 1 diabetes, and rheumatoid arthritis. Our review will focus on the main mechanisms by which helminths and their secreted molecules modulate the host's immune system. The main pathways induce a shift from Th1 to Th2 phenotype, accelerate T regulatory and B regulatory phenotypes, and attenuate the levels of the inflammatory cytokines, leading to a tolerable scenario.
在过去的半个世纪里,自身免疫性疾病的发病率一直在上升,主要集中在工业化世界。寄生虫及其衍生物被发现具有在自身免疫和炎症状态下的保护作用,因为它们可以操纵免疫网络,减弱宿主的细胞和体液反应。事实上,在几种人类和动物模型中使用的各种寄生虫物种被证明可以限制多种疾病中的炎症活动,包括炎症性肠病、多发性硬化症、1 型糖尿病和类风湿性关节炎。我们的综述将集中讨论寄生虫及其分泌分子调节宿主免疫系统的主要机制。主要途径诱导从 Th1 向 Th2 表型的转变,加速 T 调节和 B 调节表型,并减弱炎症细胞因子的水平,导致可耐受的情况。