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The mucosal immune system for vaccine development

机译:用于疫苗开发的粘膜免疫系统

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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. (C) 2014 Elsevier Ltd. All rights reserved.
机译:粘膜表面连续暴露于外部环境,因此代表了身体最大的淋巴器官。在粘膜免疫系统中,与肠道相关的淋巴组织(GALT),包括派伊尔氏淋巴结和分离的淋巴滤泡,在诱导肠道抗原特异性免疫反应中起着重要作用。 GALT具有独特的器官发生特性,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反应和口服耐受性。在这些淋巴组织中,抗原被上皮层中的M细胞吸收,抗原特异性免疫反应随后由GALT细胞启动。鼻咽和与泪液相关的淋巴组织(NALT和TALT)分别是呼吸道和眼腔中的关键组织淋巴结构,并已显示出彼此相互作用。粘膜表面的特征还在于宿主-微生物相互作用,其影响与粘膜相关的淋巴组织的形成和成熟以及先天性和获得性粘膜免疫反应的诱导和调节。由于大多数有害病原体通过食入,吸入或性接触通过粘膜表面进入人体,因此粘膜是疫苗接种的候选部位。粘膜疫苗接种具有一些生理和实用优势,例如降低成本,降低针刺伤害和血液传播疾病的风险,并且无痛。最近,现代生物工程和生化工程技术的应用,包括基因转化和操纵系统,导致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,这将开创粘膜疫苗抗原递送系统的新时代。在这篇综述中,基于我们研究小组三十七年的进步和努力,我们重点介绍了粘膜免疫系统的独特功能以及粘膜免疫在新一代疫苗开发中的应用。 (C)2014 Elsevier Ltd.保留所有权利。

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