Department of Immunology, Tongji University School of Medicine, Shanghai, China.
BMC Immunol. 2010 Jun 10;11:28. doi: 10.1186/1471-2172-11-28.
A long-term existing schistosome infection can aid in maintaining immuno-homeostasis, thus providing protection against various types of autoimmune diseases to the infected host. Such benefits have often been associated with acute or egg stage infection and with the egg-induced Th2 response. However, since schistosome infection undergoes different stages, each associated with a specific induction of Th responses, the requirements for the ability of the different stages of schistosome infection to protect against autoimmune disease has not been elucidated. The present study was designed to study whether different stages of schistosome infection offer unique protection in collagen-induced arthritis and its mechanisms.
Arthritis susceptible strain DBA/1 male mice were infected with Schistosoma japonicum for either 2 weeks resulting in early stage infection or for 7 weeks resulting in acute or egg stage infection. Following Schistosoma japonicum infection, collagen II was administered to induce collagen-induced arthritis, an animal model for human rheumatoid arthritis. Infection by Schistosoma japonicum significantly reduced the severity and the incidence of experimental autoimmune collagen-induced arthritis. However, this beneficial effect can only be provided by a pre-established acute stage of infection but not by a pre-established early stage of the infection. The protection against collagen-induced arthritis correlated with reduced levels of anti-collagen II IgG, especially the subclass of IgG2a. Moreover, in protected mice increased levels of IL-4 were present at the time of collagen II injection together with sustained higher IL-4 levels during the course of arthritis development. In contrast, in unprotected mice minimal levels of IL-4 were present at the initial stage of collagen II challenge together with lack of IL-4 induction following Schistosoma japonicum infection.
The protective effect against collagen-induced arthritis provided by Schistosoma japonicum infection is infection stage-dependent. Furthermore, the ability of schistosomiasis to negatively regulate the onset of collagen-induced arthritis is associated with a dominant as well as long-lasting Th2 response at the initiation and development of autoimmune joint and systemic inflammation.
长期存在的血吸虫感染有助于维持免疫稳态,从而为感染宿主提供对各种自身免疫性疾病的保护。这种益处通常与急性或虫卵期感染以及卵诱导的 Th2 反应有关。然而,由于血吸虫感染经历不同的阶段,每个阶段都与特定的 Th 反应诱导相关,因此不同阶段的血吸虫感染保护宿主免受自身免疫性疾病的能力尚未阐明。本研究旨在研究血吸虫感染的不同阶段是否在胶原诱导性关节炎及其机制中提供独特的保护。
关节炎易感株 DBA/1 雄性小鼠感染日本血吸虫 2 周导致早期感染或感染 7 周导致急性或虫卵期感染。感染日本血吸虫后,给予 II 型胶原诱导胶原诱导性关节炎,这是一种人类类风湿关节炎的动物模型。日本血吸虫感染显著减轻了实验性自身免疫性胶原诱导性关节炎的严重程度和发生率。然而,这种有益作用只能由预先建立的急性感染阶段提供,而不能由预先建立的早期感染阶段提供。对胶原诱导性关节炎的保护与抗胶原 II IgG 水平降低相关,尤其是 IgG2a 亚类。此外,在受保护的小鼠中,在注射 II 型胶原时存在更高水平的 IL-4,并且在关节炎发展过程中持续存在更高水平的 IL-4。相比之下,在未受保护的小鼠中,在 II 型胶原挑战的初始阶段存在最低水平的 IL-4,并且在日本血吸虫感染后缺乏 IL-4 诱导。
日本血吸虫感染对胶原诱导性关节炎的保护作用取决于感染阶段。此外,血吸虫病对胶原诱导性关节炎发病的负调节作用与在自身免疫性关节和系统性炎症的发生和发展时起始和持续的主导 Th2 反应相关。