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用于炎症性肠病的精准微生物群疗法:前提与前景。

Precision microbiota therapy for IBD: premise and promise.

作者信息

Nagayama Manabu, Gogokhia Lasha, Longman Randy S

机构信息

Jill Roberts Institute for Research in Inflammatory Bowel Disease, Weill Cornell Medicine, New York, NY, USA.

Jill Roberts Center for Inflammatory Bowel Disease, Division of Gastroenterology and Hepatology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

出版信息

Gut Microbes. 2025 Dec;17(1):2489067. doi: 10.1080/19490976.2025.2489067. Epub 2025 Apr 7.

Abstract

Inflammatory Bowel Disease (IBD) is a spectrum of chronic inflammatory diseases of the intestine that includes subtypes of ulcerative colitis (UC) and Crohn's Disease (CD) and currently has no cure. While IBD results from a complex interplay between genetic, environmental, and immunological factors, sequencing advances over the last 10-15 years revealed signature changes in gut microbiota that contribute to the pathogenesis of IBD. These findings highlight IBD as a disease target for microbiome-based therapies, with the potential to treat the underlying microbial pathogenesis and provide adjuvant therapy to the emerging spectrum of advanced therapies for IBD. Building on the success of fecal microbiota transplantation (FMT) for infection, therapies targeting gut microbiota have emerged as promising approaches for treating IBD; however, unique aspects of IBD pathogenesis highlight the need for more precision in the approach to microbiome therapeutics that leverage aspects of recipient and donor selection, diet and xenobiotics, and strain-specific interactions to enhance the efficacy and safety of IBD therapy. This review focuses on both pre-clinical and clinical studies that support the premise for microbial therapeutics for IBD and aims to provide a framework for the development of precision microbiome therapeutics to optimize clinical outcomes for patients with IBD.

摘要

炎症性肠病(IBD)是一种肠道慢性炎症性疾病谱,包括溃疡性结肠炎(UC)和克罗恩病(CD)亚型,目前尚无治愈方法。虽然IBD是由遗传、环境和免疫因素之间复杂的相互作用引起的,但过去10至15年测序技术的进步揭示了肠道微生物群的特征性变化,这些变化促成了IBD的发病机制。这些发现凸显了IBD作为基于微生物群疗法的疾病靶点,有潜力治疗潜在的微生物发病机制,并为IBD新兴的一系列先进疗法提供辅助治疗。基于粪便微生物群移植(FMT)治疗感染的成功,针对肠道微生物群的疗法已成为治疗IBD的有前景的方法;然而,IBD发病机制的独特方面凸显了在微生物群治疗方法上需要更高的精准度,即利用受者和供者选择、饮食和外源性物质以及菌株特异性相互作用等方面来提高IBD治疗的疗效和安全性。本综述重点关注支持IBD微生物治疗前提的临床前和临床研究,旨在为精准微生物群治疗的发展提供一个框架,以优化IBD患者的临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2987/11980506/52f344e5e555/KGMI_A_2489067_F0001_OC.jpg

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