Division of Biochemistry, Faculty of Pharmacy and Graduate School of Pharmaceutical Sciences, Keio University, Minato-ku, Tokyo, Japan.
International Research and Development Center for Mucosal Vaccines, The Institute of Medical Science, The University of Tokyo (IMSUT), Minato-ku, Tokyo, Japan.
Int Immunol. 2021 Nov 25;33(12):755-759. doi: 10.1093/intimm/dxab051.
The intestinal immune system maintains intestinal homeostasis in collaboration with diverse immune cell subsets residing at the epithelial layer, lamina propria and gut-associated lymphoid tissue (GALT). Bacterial components and their metabolites are essential for the establishment of the gut immune system. In addition, nutritional signals contribute to maintaining the mucosal immune response. Specialized epithelial microfold (M) cells in GALT facilitate immune surveillance on the mucosal surface by actively taking up external antigens to transport them into the lymphoid follicles. Because hyperplasia of M cells causes an excessive immune response in GALT, there is a self-regulatory mechanism to control the development of M cells appropriately. In this review, we will discuss the molecular mechanisms of mucosal immune regulation and their biological importance.
肠道免疫系统与位于上皮层、固有层和肠相关淋巴组织 (GALT) 的多种免疫细胞亚群合作,维持肠道内环境稳态。细菌成分及其代谢物对于肠道免疫系统的建立至关重要。此外,营养信号有助于维持黏膜免疫反应。GALT 中的特化上皮微皱褶 (M) 细胞通过主动摄取外源性抗原并将其运送到淋巴滤泡中,促进黏膜表面的免疫监视。由于 M 细胞的增生会导致 GALT 中过度的免疫反应,因此存在一种自我调节机制来适当控制 M 细胞的发育。在这篇综述中,我们将讨论黏膜免疫调节的分子机制及其生物学意义。