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黏膜免疫系统:从牙科学到疫苗研发

The mucosal immune system: From dentistry to vaccine development.

作者信息

Kiyono Hiroshi, Azegami Tatsuhiko

机构信息

Division of Mucosal Immunology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo.

出版信息

Proc Jpn Acad Ser B Phys Biol Sci. 2015;91(8):423-39. doi: 10.2183/pjab.91.423.

Abstract

The oral cavity is the beginning of the aero-digestive tract, which is covered by mucosal epithelium continuously under the threat of invasion of pathogens, it is thus protected by the mucosal immune system. In the early phase of our scientific efforts for the demonstration of mucosal immune system, dental science was one of major driving forces due to their foreseeability to use oral immunity for the control of oral diseases. The mucosal immune system is divided functionally into, but interconnected inductive and effector sites. Intestinal Peyer's patches (PPs) are an inductive site containing antigen-sampling M cells and immunocompetent cells required to initiate antigen-specific immune responses. At effector sites, PP-originated antigen-specific IgA B cells become plasma cells to produce polymeric IgA and form secretory IgA by binding to poly-Ig receptor expressed on epithelial cells for protective immunity. The development of new-generation mucosal vaccines, including the rice-based oral vaccine MucoRice, on the basis of the coordinated mucosal immune system is a promising strategy for the control of mucosal infectious diseases.

摘要

口腔是气消化道的起始部位,其被黏膜上皮覆盖,持续面临病原体入侵的威胁,因此受到黏膜免疫系统的保护。在我们为证明黏膜免疫系统而开展科学研究的早期阶段,牙科科学是主要驱动力之一,因为其预见到可利用口腔免疫来控制口腔疾病。黏膜免疫系统在功能上分为相互连接的诱导部位和效应部位。肠道派尔集合淋巴结(PPs)是一个诱导部位,含有启动抗原特异性免疫反应所需的抗原采样M细胞和免疫活性细胞。在效应部位,源自PPs的抗原特异性IgA B细胞成为浆细胞,产生聚合IgA,并通过与上皮细胞上表达的多聚Ig受体结合形成分泌型IgA,以提供保护性免疫。基于协调的黏膜免疫系统开发新一代黏膜疫苗,包括基于水稻的口服疫苗MucoRice,是控制黏膜传染病的一种有前景的策略。

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