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黏膜防御在肠道上皮细胞界面。

Mucosal Defense Against at the Intestinal Epithelial Cell Interface.

机构信息

Laboratory of Mucosal Immunology, Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, United States.

出版信息

Front Immunol. 2022 Feb 17;13:817468. doi: 10.3389/fimmu.2022.817468. eCollection 2022.

Abstract

Human giardiasis, caused by the protozoan parasite (syn. , , ), is one of the most commonly-identified parasitic diseases worldwide. Chronic infections cause a malabsorption syndrome that may lead to failure to thrive and/or stunted growth, especially in children in developing countries. Understanding the parasite/epithelial cell crosstalk at the mucosal surfaces of the small intestine during human giardiasis may provide novel insights into the mechanisms underlying the parasite-induced immunopathology and epithelial tissue damage, leading to malnutrition. Efforts to identify new targets for intervening in the development of intestinal immunopathology and the progression to malnutrition are critical. Translating these findings into a clinical setting will require analysis of these pathways in cells and tissues from humans and clinical trials could be devised to determine whether interfering with unwanted mucosal immune responses developed during human giardiasis provide better therapeutic benefits and clinical outcomes for infections in humans.

摘要

人类贾第虫病是由原生动物寄生虫(同义词、、)引起的,是世界范围内最常见的寄生虫病之一。慢性感染会导致吸收不良综合征,可能导致发育不良和/或生长迟缓,尤其是在发展中国家的儿童中。了解人类贾第虫病期间小肠黏膜表面的寄生虫/上皮细胞相互作用,可能为寄生虫引起的免疫病理学和上皮组织损伤导致营养不良的机制提供新的见解。努力确定干预肠道免疫病理学发展和营养不良进展的新靶点至关重要。将这些发现转化为临床环境需要分析来自人类的细胞和组织中的这些途径,并且可以设计临床试验来确定是否干扰人类贾第虫病期间发生的不良黏膜免疫反应为人类感染提供更好的治疗益处和临床结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeaa/8891505/a5b516e8dcf5/fimmu-13-817468-g001.jpg

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