Clare Simon, Huett Alan, Dougan Gordon
Centre for Molecular Microbiology and Infection, Department of Biological Sciences, Imperial College of Science, Technology and Medicine, London, UK.
Res Microbiol. 2002 Sep;153(7):455-9. doi: 10.1016/s0923-2508(02)01345-1.
The mucosal immune system has evolved to protect the host against the establishment of infections at or through the mucosal surfaces of the body. Protective immunity must be activated to specific pathogenic agents or their products but inappropriate immune responses to food/environmental antigens must be avoided. Thus, the mucosal immune system is under tight regulation. Pathogenic bacteria and their products can be exploited as specific probes of mucosal immune responses. Bacterial enterotoxins such as cholera toxin are potent mucosal immunogens and adjuvants that activate both mucosal and systemic immune responses. Infection models involving microorganisms such as Citrobacter rodentium can also be used to investigate the consequences of mucosal colonisation that lead to immune disfunction.
黏膜免疫系统不断进化,以保护宿主抵御在身体黏膜表面或通过黏膜表面发生的感染。必须针对特定病原体或其产物激活保护性免疫,但要避免对食物/环境抗原产生不适当的免疫反应。因此,黏膜免疫系统受到严格调控。病原菌及其产物可用作黏膜免疫反应的特异性探针。诸如霍乱毒素之类的细菌肠毒素是强效的黏膜免疫原和佐剂,可激活黏膜和全身免疫反应。涉及鼠柠檬酸杆菌等微生物的感染模型也可用于研究导致免疫功能紊乱的黏膜定植后果。