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Mucosal Immunosenescence In The Gastrointestinal Tract

机译:胃肠道粘膜免疫衰老

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摘要

It has been shown that pathogen-specific secretory IgA (SIgA) antibody (Ab) is the major player at mucosal surfaces for host defense. However, alterations in the mucosal immune system occur in advanced aging which results in a failure of induction of SIgA Abs for protection from infectious diseases. Signs of mucosal senescence first appear in the gut immune system. Further, changes in the intestinal microbiota most likely influence mucosal immunity. To overcome the immunological aging decline in mucosal immunity, several adjuvant systems including mucosal dendritic cell (DC) targeting have been shown to be attractive and effective immunological strategies. Similarly, antigen (Ag) uptake-M cells are ideal targets for facilitating Ag-specific mucosal immune responses. However, the numbers of M cells are reduced in aged mice. In this regard, Spi-B, an essential transcription factor for the functional and structural differentiation of M cells could be a potent strategy for the induction of effective mucosal immunity in aging.
机译:已经显示,病原体特异性分泌型IgA(SIgA)抗体(Ab)是粘膜表面宿主防御的主要参与者。然而,粘膜免疫系统的改变在晚期衰老中发生,这导致不能诱导SIgA Abs以免于感染性疾病的保护。粘膜衰老的迹象首先出现在肠道免疫系统中。此外,肠道菌群的变化最有可能影响粘膜免疫力。为了克服粘膜免疫的免疫衰老下降,已经证明包括粘膜树突状细胞(DC)靶向在内的几种佐剂系统是有吸引力且有效的免疫策略。同样,抗原(Ag)摄取M细胞是促进Ag特异性粘膜免疫反应的理想靶标。但是,老年小鼠的M细胞数量减少了。在这方面,Spi-B是M细胞功能和结构分化的必需转录因子,可能是在衰老过程中诱导有效粘膜免疫的有效策略。

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