Engineered live bacteria for liver diseases and gut-liver axis disorders: from genetic modification to advanced delivery systems.
Yanan Zhang, Yawen Zhu, Yun Yang, Dayu Chen et al.
Kernaussage
Engineered live bacteria, including strains like Bifidobacterium, E. coli Nissle 1917, and Bacillus subtilis, demonstrate therapeutic potential for liver diseases by modulating the gut-liver axis, but clinical translation is hindered by insufficient validation and a lack of disease-specific standards.
Abstract
Liver diseases, including hepatocellular carcinoma (HCC), non-alcoholic fatty liver disease (NAFLD), and alcoholic liver disease (ALD), impose a significant global health burden, with over 2 million deaths annually and substantial economic losses. Current treatments, primarily pharmacological, face challenges such as insufficient efficacy, poor absorption, and drug resistance. The liver-gut axis, a critical pathway linking the liver and intestines, offers a therapeutic target for these diseases. Engineered live bacteria, modified through genetic engineering and synthetic biology, have emerged as a promising alternative. These bacteria can be designed to deliver therapeutic agents directly to the liver or gut, enhancing efficacy and reducing systemic side effects. This review explores the application of engineered live bacteria in treating liver diseases, focusing on strains such as Bifidobacterium, Escherichia coli Nissle 1917 (EcN), Bacillus subtilis (B. subtilis), Saccharomyces boulardii (S. boulardii), and Lactobacillus reuteri (L. reuteri). It also pays attention to the internal genetic modification and external covalent connection of the original live bacteria. We discuss the design of dosage forms, including capsule formulations, microencapsulation, and nanopreparations, and administration methods like oral and in situ injection. Additionally, we address the challenges and future prospects of using engineered live bacteria to target liver diseases and related conditions, aiming to advance their clinical application and reduce the global burden of liver diseases.
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Quelle: PubMed Central / National Library of Medicine (NLM). Apollion steht in keiner Verbindung mit NLM und wird von NLM nicht empfohlen. Evidenzgrade bewerten die methodische Studienqualität — nicht die inhaltliche Richtigkeit.
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