Stavitsky A B, Olds G R
Infect Immun. 1986 Nov;54(2):590-2. doi: 10.1128/iai.54.2.590-592.1986.
Schistosoma japonicum-infected mice develop hepatic granulomas, immediate hypersensitivity (IH), and delayed hypersensitivity (DH) to soluble egg antigens (SEA) released by parasite eggs trapped in liver sinusoids. All of these responses spontaneously regress after 7 to 9 weeks of infection. This study aimed to develop an in vivo system for the further dissection of cellular and humoral immune responses to SEA. C57BL/6 mice immunized subcutaneously with SEA in complete Freund adjuvant developed IH, an Arthus reaction, and DH to this antigen 5 to 9 days later. IH and the Arthus reaction, but not DH, were markedly inhibited if, 1 day before injection of SEA in complete Freund adjuvant, the mice were injected intravenously with purified T cells from the spleens of mice infected for at least 9 weeks. This in vivo model system can be used to study various aspects of cellular and humoral immune responses to SEA and their modulation. These results raise questions about the role of antibodies in the pathogenesis of granulomatous inflammation and about the mechanisms of its cellular regulation in infections with S. japonicum.
感染日本血吸虫的小鼠会形成肝肉芽肿、速发型超敏反应(IH)以及对被困在肝血窦中的寄生虫卵释放的可溶性虫卵抗原(SEA)的迟发型超敏反应(DH)。在感染7至9周后,所有这些反应会自发消退。本研究旨在开发一种体内系统,用于进一步剖析对SEA的细胞免疫和体液免疫反应。用SEA在完全弗氏佐剂中皮下免疫的C57BL/6小鼠在5至9天后对该抗原产生了IH、阿瑟氏反应和DH。如果在将SEA注射到完全弗氏佐剂中前1天,给小鼠静脉注射来自感染至少9周的小鼠脾脏的纯化T细胞,那么IH和阿瑟氏反应会受到显著抑制,但DH不受影响。这个体内模型系统可用于研究对SEA的细胞免疫和体液免疫反应的各个方面及其调节。这些结果引发了关于抗体在肉芽肿性炎症发病机制中的作用以及日本血吸虫感染中其细胞调节机制的问题。