Engineered probiotics for inflammatory bowel disease therapy: mechanisms, delivery strategies, and precision medicine

炎症性肠病 精密医学 医学 溃疡性结肠炎 个性化医疗 微生物群 疾病 益生菌 免疫系统 生物信息学 炎症性肠病 转化医学 重症监护医学 免疫学 计算生物学 肠道菌群 临床实习 克罗恩病 转化研究 失调 肠易激综合征 结肠炎 临床试验 肠道微生物群 系统生物学 临床疗效 疾病治疗 基因工程 遗传增强 不利影响
作者
X. Wang,Yindi Cheng,Jiahui Huang,Feixuan Xu,Jian Jiang,Nonthaneth Nalinratana,Litong Jin,Ying Xue
出处
期刊:Frontiers in Microbiology [Frontiers Media]
卷期号:16: 1696524-1696524 被引量:6
标识
DOI:10.3389/fmicb.2025.1696524
摘要

Inflammatory bowel disease (IBD), encompassing ulcerative colitis (UC) and Crohn’s disease (CD), is a prevalent chronic gastrointestinal disorder. Conventional therapies are often limited by adverse effects and suboptimal long-term efficacy. Probiotics have emerged as promising therapeutic alternatives for IBD because of their ability to modulate the gut microbiota, reinforce intestinal barrier integrity, and regulate immune responses. However, their clinical translation is hampered by challenges within the harsh gastrointestinal milieu, including low viability, poor colonization, and insufficient target specificity. This review focuses on the engineering of probiotics designed to overcome these limitations for IBD management. We outline the therapeutic potential and mechanisms of action of probiotics in IBD, with a critical emphasis on discrepancies between preclinical and clinical observations. We subsequently discuss the drawbacks of conventional probiotic therapies, highlighting gaps between in vitro efficacy and in vivo performance. We then highlight cutting-edge engineering strategies, encompassing advanced encapsulation techniques, genetic engineering approaches, novel delivery systems, and molecular-targeting modifications, with quantitative comparisons of their advantages, limitations, and translational potential. The application of these engineered probiotics specifically in UC and CD treatment is explored, with detailed analyses of preclinical models and clinical trials. We also address personalized interventions tailored to individual gut microbiome profiles. Despite significant promise, critical challenges remain, including long-term safety, stability, and accurate prediction of therapeutic responses for engineered probiotics in IBD. Nevertheless, with ongoing advancements in gene editing, synthetic biology, and microbial safety engineering, engineered probiotics represent a promising direction in IBD therapy that will enable more precise, effective, and personalized treatment modalities, provided that safety, reproducibility, and regulatory compliance are prioritized.
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