Engineered probiotics with sustained release of interleukin-2 for the treatment of inflammatory bowel disease after oral delivery

炎症性肠病 免疫系统 益生菌 肠道菌群 胃肠道 医学 炎症 肠上皮 生物 免疫学 微生物学 疾病 内科学 上皮 细菌 生物化学 遗传学
作者
Maoyi Li,Nanhui Liu,Jiafei Zhu,Yumin Wu,Le Niu,Yi Liu,Linfu Chen,Boxiong Bai,Miao Yu,Yang Yang,Qian Chen,Qian Chen
出处
期刊:Biomaterials [Elsevier BV]
卷期号:309: 122584-122584 被引量:69
标识
DOI:10.1016/j.biomaterials.2024.122584
摘要

Inflammatory bowel disease (IBD) is a kind of auto-immune disease characterized by disrupted intestinal barrier and mucosal epithelium, imbalanced gut microbiome and deregulated immune responses. Therefore, the restoration of immune equilibrium and gut microbiota could potentially serve as a hopeful approach for treating IBD. Herein, the oral probiotic Escherichia coli Nissle 1917 (ECN) was genetically engineered to express secretable interleukin-2 (IL-2), a kind of immunomodulatory agent, for the treatment of IBD. In our design, probiotic itself has the ability to regulate the gut microenvironment and IL-2 at low dose could selectively promote the generation of regulatory T cells to elicit tolerogenic immune responses. To improve the bioavailability of ECN expressing IL-2 (ECN-IL2) in the gastrointestinal tract, enteric coating Eudragit L100-55 was used to coat ECN- IL2, achieving significantly enhanced accumulation of engineered probiotics in the intestine. More importantly, L100-55 coated ECN-IL2 could effectively activated Treg cells to regulate innate immune responses and gut microbiota, thereby relieve inflammation and repair the colon epithelial barrier in dextran sodium sulfate (DSS) induced IBD. Therefore, genetically and chemically modified probiotics with excellent biocompatibility and efficiency in regulating intestinal microflora and intestinal inflammation show great potential for IBD treatment in the future.
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