Lamichhane Aayam, Azegamia Tatsuhiko, Kiyonoa Hiroshi
Division of Mucosal Immunology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Vaccine. 2014 Nov 20;32(49):6711-23. doi: 10.1016/j.vaccine.2014.08.089.
Mucosal surfaces are continuously exposed to the external environment and therefore represent the largest lymphoid organ of the body. In the mucosal immune system, gut-associated lymphoid tissues (GALTs), including Peyer's patches and isolated lymphoid follicles, play an important role in the induction of antigen-specific immune responses in the gut. GALTs have unique organogenesis characteristics and interact with the network of dendritic cells and T cells for the simultaneous induction and regulation of IgA responses and oral tolerance. In these lymphoid tissues, antigens are up taken by M cells in the epithelial layer, and antigen-specific immune responses are subsequently initiated by GALT cells. Nasopharynx- and tear-duct-associated lymphoid tissues (NALTs and TALTs) are key organized lymphoid structures in the respiratory tract and ocular cavities, respectively, and have been shown to interact with each other. Mucosal surfaces are also characterized by host-microbe interactions that affect the genesis and maturation of mucosa-associated lymphoid tissues and the induction and regulation of innate and acquired mucosal immune responses. Because most harmful pathogens enter the body through mucosal surfaces by ingestion, inhalation, or sexual contact, the mucosa is a candidate site for vaccination. Mucosal vaccination has some physiological and practical advantages, such as decreased costs and reduced risk of needle-stick injuries and transmission of bloodborne diseases, and it is painless. Recently, the application of modern bioengineering and biochemical engineering technologies, including gene transformation and manipulation systems, resulted in the development of systems to express vaccine antigens in transgenic plants and nanogels, which will usher in a new era of delivery systems for mucosal vaccine antigens. In this review, based on some of our research group's thirty seven years of progress and effort, we highlight the unique features of mucosal immune systems and the application of mucosal immunity to the development of a new generation of vaccines.
黏膜表面持续暴露于外部环境,因此是人体最大的淋巴器官。在黏膜免疫系统中,肠道相关淋巴组织(GALT),包括派尔集合淋巴结和孤立淋巴滤泡,在肠道内诱导抗原特异性免疫反应中发挥重要作用。GALT具有独特的器官发生特征,并与树突状细胞和T细胞网络相互作用,以同时诱导和调节IgA反应及口服耐受性。在这些淋巴组织中,抗原被上皮层中的M细胞摄取,随后由GALT细胞启动抗原特异性免疫反应。鼻咽和泪管相关淋巴组织(NALT和TALT)分别是呼吸道和眼腔中的关键有组织淋巴结构,并且已显示它们之间会相互作用。黏膜表面的特征还在于宿主与微生物的相互作用,这种相互作用会影响黏膜相关淋巴组织的发生和成熟以及先天和后天黏膜免疫反应的诱导和调节。由于大多数有害病原体通过摄入、吸入或性接触经黏膜表面进入人体,因此黏膜是疫苗接种的候选部位。黏膜疫苗接种具有一些生理和实际优势,例如成本降低、针刺伤风险降低以及血源性病原体传播风险降低,并且无痛。最近,包括基因转化和操纵系统在内的现代生物工程和生化工程技术的应用,促成了在转基因植物和纳米凝胶中表达疫苗抗原的系统的开发,这将开创黏膜疫苗抗原递送系统的新时代。在本综述中,基于我们研究团队三十七年的一些进展和努力,我们重点介绍了黏膜免疫系统的独特特征以及黏膜免疫在新一代疫苗开发中的应用。