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经纳米医学训练的肠道微生物群的细胞外囊泡可替代粪便微生物群移植治疗溃疡性结肠炎。

Extracellular Vesicles from Nanomedicine-Trained Intestinal Microbiota Substitute for Fecal Microbiota Transplant in Treating Ulcerative Colitis.

机构信息

Department of Pharmacy, Personalized Drug Therapy Key Laboratory of Sichuan Province, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610054, China.

State Key Laboratory of Resource Insects, College of Sericulture, Textile, and Biomass Sciences, Southwest University, Chongqing, 400715, China.

出版信息

Adv Mater. 2024 Oct;36(41):e2409138. doi: 10.1002/adma.202409138. Epub 2024 Jul 29.

DOI:10.1002/adma.202409138
PMID:39073205
Abstract

The biosafety concerns associated with fecal microbiota transplant (FMT) limit their clinical application in treating ulcerative colitis (UC). Gut microbiota secrete abundant extracellular vesicles (Gm-EVs), which play a critical role in bacteria-to-bacteria and bacteria-to-host communications. Herein, intestinal microbiota are trained using tea leaf lipid/pluronic F127-coated curcumin nanocrystals (CN@Lps), which can maintain stability during transit through the gastrointestinal tract. Compared with FMT, Gm-EVs derived from healthy mice significantly improve treatment outcomes against UC by reducing colonic inflammatory responses, restoring colonic barrier function, and rebalancing intestinal microbiota. Strikingly, Gm-EVs obtained from CN@Lp-trained healthy mice exhibit a superior therapeutic effect on UC compared to groups receiving FMT from healthy mice, Gm-EVs from healthy mice, and FMT from CN@Lp-trained healthy mice. Oral administration of Gm-EVs from CN@Lp-trained healthy mice not only alleviates colonic inflammation, promotes mucosal repair, and regulates gut microbiota but also regulates purine metabolism to decrease the uric acid level, resulting in a robust improvement in the UC. This study demonstrates the UC therapeutic efficacy of Gm-EVs derived from nanomedicine-trained gut microbiota in regulating the immune microenvironment, microbiota, and purine metabolism of the colon. These EVs provide an alternative platform to replace FMT as a treatment for UC.

摘要

与粪便微生物群移植 (FMT) 相关的生物安全问题限制了其在治疗溃疡性结肠炎 (UC) 中的临床应用。肠道微生物群分泌丰富的细胞外囊泡 (Gm-EVs),在细菌间和细菌与宿主间的通讯中发挥着关键作用。在此,使用茶叶脂质/普朗尼克 F127 涂层姜黄素纳米晶体 (CN@Lps) 对肠道微生物群进行训练,该纳米晶体可以在通过胃肠道的过程中保持稳定。与 FMT 相比,来自健康小鼠的 Gm-EVs 通过减少结肠炎症反应、恢复结肠屏障功能和平衡肠道微生物群,显著改善了 UC 的治疗效果。值得注意的是,与接受来自健康小鼠的 FMT、来自健康小鼠的 Gm-EVs 和来自经 CN@Lp 训练的健康小鼠的 FMT 的小鼠相比,来自经 CN@Lp 训练的健康小鼠的 Gm-EVs 对 UC 具有更好的治疗效果。口服来自经 CN@Lp 训练的健康小鼠的 Gm-EVs 不仅可以缓解结肠炎症、促进黏膜修复和调节肠道微生物群,还可以调节嘌呤代谢以降低尿酸水平,从而使 UC 得到显著改善。本研究证明了源自纳米医学训练的肠道微生物群的 Gm-EVs 调节结肠免疫微环境、微生物群和嘌呤代谢的 UC 治疗功效。这些 EVs 提供了一个替代 FMT 的平台,作为 UC 的治疗方法。

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