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肠道微生物群通过桥接免疫和脂质代谢。

Bridging immunity and lipid metabolism by gut microbiota.

机构信息

College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331, USA.

出版信息

J Allergy Clin Immunol. 2013 Aug;132(2):253-62; quiz 263. doi: 10.1016/j.jaci.2013.06.025.

Abstract

The human gut is a unique organ in which hundreds of different microbial species find their habitat and in which different host physiologic functions, such as digestion, nutrition, and immunity, coexist. Although all these players were studied separately for decades, recently, there has been an explosion of studies demonstrating the essential role for interactions between these components in gut function. Furthermore, new systems biology methods provide essential tools to study this complex system as a whole and to identify key elements that define the crosstalk between the gut microbiota, immunity, and metabolism. This review is devoted to several human diseases resulting from the disruption in this crosstalk, including immunodeficiency-associated and environmental enteropathies, celiac disease, inflammatory bowel disease, and obesity. We describe findings in experimental models of these diseases and in germ-free animals that help us understand the mechanisms and test new therapeutic strategies. We also discuss current challenges that the field is facing and propose that a new generation of antibiotics, prebiotics, and probiotics coupled with novel, systems biology-driven diagnostics will provide the basis for future personalized therapy.

摘要

人类肠道是一个独特的器官,其中有数百种不同的微生物物种栖息于此,同时也共存着不同的宿主生理功能,如消化、营养和免疫。尽管这些参与者已经被单独研究了几十年,但最近,大量研究表明这些成分之间的相互作用对于肠道功能至关重要。此外,新的系统生物学方法为研究这个复杂的整体系统提供了必要的工具,并确定了定义肠道微生物群、免疫和代谢之间串扰的关键要素。这篇综述专门讨论了由于这种串扰中断而导致的几种人类疾病,包括免疫缺陷相关和环境肠病、乳糜泻、炎症性肠病和肥胖症。我们描述了这些疾病的实验模型和无菌动物中的发现,这些发现帮助我们了解了这些疾病的发病机制并测试了新的治疗策略。我们还讨论了该领域目前面临的挑战,并提出新一代抗生素、益生元和益生菌,再加上新型的、基于系统生物学的诊断方法,将为未来的个性化治疗提供基础。

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