Tsuji Masayuki, Suzuki Keiichiro, Kinoshita Kazuo, Fagarasan Sidonia
Laboratory for Mucosal Immunity, RIKEN Research Center for Allergy and Immunology, 230-0045 Tsurumi, Yokohama, Japan.
Semin Immunol. 2008 Feb;20(1):59-66. doi: 10.1016/j.smim.2007.12.003. Epub 2008 Feb 1.
The gastrointestinal tract is colonized by an immense number of bacteria that are in a constant dialog with our immune cells. One obvious question is how the mucosal immune system maintains a state of hypo-responsiveness toward the commensal bacteria and a state of readiness that allows efficient and prompt responses against pathogens. The answers have important implications for immunologists who seek to understand the fundamental aspects of bacteria-immune cell interactions in the steady-state condition and wish to elucidate the patho-physiologic mechanisms in immune disregulations, such as inflammatory bowel diseases. An important adjustment of the immune system to bacterial colonization of the gut is the "constitutive" production of IgA by the gut-associated lymphoid tissues (GALT). In this review, we summarize the sites and mechanisms for IgA synthesis in mice. We emphasize the important role played by secretory IgAs in maintenance of an appropriate intestinal microbiota, which is required for local and systemic immune homeostasis.
胃肠道中定植着大量细菌,它们与我们的免疫细胞不断进行对话。一个显而易见的问题是,黏膜免疫系统如何维持对共生细菌的低反应状态以及对病原体做出有效快速反应的准备状态。这些答案对于那些试图理解稳态条件下细菌与免疫细胞相互作用的基本方面,并希望阐明免疫失调(如炎症性肠病)病理生理机制的免疫学家具有重要意义。免疫系统对肠道细菌定植的一个重要调节是肠道相关淋巴组织(GALT)“组成性”产生IgA。在本综述中,我们总结了小鼠体内IgA合成的部位和机制。我们强调分泌型IgA在维持适当肠道微生物群方面所起的重要作用,而这是局部和全身免疫稳态所必需的。