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

被引:9
作者
Li, Maoyi [1 ]
Liu, Nanhui [1 ]
Zhu, Jiafei [1 ]
Wu, Yumin [1 ]
Niu, Le [1 ]
Liu, Yi [2 ]
Chen, Linfu [1 ]
Bai, Boxiong [1 ]
Miao, Yu [1 ]
Yang, Yang [2 ]
Chen, Qian [1 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
[2] Tongji Univ, Shanghai Pulm Hosp, Sch Med, Dept Thorac Surg, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Engineered probiotics; Interleukin-2; Inflammatory bowel disease; Chemical modification; Oral delivery;
D O I
10.1016/j.biomaterials.2024.122584
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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 ECNIL2, 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.
引用
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页数:12
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