粪便微生物群移植及其他肠道微生物群调控策略

Fecal Microbiota Transplantation and Other Gut Microbiota Manipulation Strategies.

作者信息

Quaranta Gianluca, Guarnaccia Alessandra, Fancello Giovanni, Agrillo Chiara, Iannarelli Federica, Sanguinetti Maurizio, Masucci Luca

机构信息

Department of Laboratory and Infectious Sciences, A. Gemelli University Hospital IRCCS, 00168 Rome, Italy.

Department of Basic Biotechnological Sciences, Intensivological and Perioperative Clinics, Catholic University of Sacred Heart, 00168 Rome, Italy.

出版信息

Microorganisms. 2022 Dec 7;10(12):2424. doi: 10.3390/microorganisms10122424.

Abstract

The gut microbiota is composed of bacteria, archaea, phages, and protozoa. It is now well known that their mutual interactions and metabolism influence host organism pathophysiology. Over the years, there has been growing interest in the composition of the gut microbiota and intervention strategies in order to modulate it. Characterizing the gut microbial populations represents the first step to clarifying the impact on the health/illness equilibrium, and then developing potential tools suited for each clinical disorder. In this review, we discuss the current gut microbiota manipulation strategies available and their clinical applications in personalized medicine. Among them, FMT represents the most widely explored therapeutic tools as recent guidelines and standardization protocols, not only for intestinal disorders. On the other hand, the use of prebiotics and probiotics has evidence of encouraging findings on their safety, patient compliance, and inter-individual effectiveness. In recent years, avant-garde approaches have emerged, including engineered bacterial strains, phage therapy, and genome editing (CRISPR-Cas9), which require further investigation through clinical trials.

摘要

肠道微生物群由细菌、古菌、噬菌体和原生动物组成。现在人们已经清楚地知道,它们之间的相互作用和新陈代谢会影响宿主生物体的病理生理学。多年来,人们对肠道微生物群的组成以及调节它的干预策略越来越感兴趣。表征肠道微生物种群是阐明其对健康/疾病平衡影响的第一步,然后开发适合每种临床疾病的潜在工具。在这篇综述中,我们讨论了目前可用的肠道微生物群操纵策略及其在个性化医学中的临床应用。其中,粪菌移植作为最近的指南和标准化方案,是探索最广泛的治疗工具,不仅用于肠道疾病。另一方面,益生元和益生菌的使用在其安全性、患者依从性和个体间有效性方面有令人鼓舞的发现。近年来,出现了一些前沿方法,包括工程菌株、噬菌体疗法和基因组编辑(CRISPR-Cas9),这些方法需要通过临床试验进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b1/9781458/81e66d9c482f/microorganisms-10-02424-g001.jpg

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