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Engineered E. coli Nissle 1917 for the delivery of matrix-tethered therapeutic domains to the gut

机译:用于将Matrix-Tethered治疗域输送到肠道的E. Coli Nissle 1917

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摘要

Mucosal healing plays a critical role in combatting the effects of inflammatory bowel disease, fistulae and ulcers. While most treatments for such diseases focus on systemically delivered anti-inflammatory drugs, often leading to detrimental side effects, mucosal healing agents that target the gut epithelium are underexplored. We genetically engineer Escherichia coli Nissle 1917 (EcN) to create fibrous matrices that promote gut epithelial integrity in situ. These matrices consist of curli nanofibers displaying trefoil factors (TFFs), known to promote intestinal barrier function and epithelial restitution. We confirm that engineered EcN can secrete the curli-fused TFFs in vitro and in vivo, and is non-pathogenic. We observe enhanced protective effects of engineered EcN against dextran sodium sulfate-induced colitis in mice, associated with mucosal healing and immunomodulation. This work lays a foundation for the development of a platform in which the in situ production of therapeutic protein matrices from beneficial bacteria can be exploited.
机译:粘膜愈合在打击炎症性肠病,瘘管和溃疡的影响方面发挥着关键作用。虽然大多数治疗这种疾病的治疗侧重于全身递送的抗炎药,通常导致靶向肠道上皮的粘膜愈合剂是望远镜的。我们转基地工程师Escherichia Coli Nissle 1917(ECN)以产生纤维基质,促进肠道上皮完整性。这些基质由卷曲纳米纤维组成,显示出促进肠道屏障功能和上皮恢复的三叶子因子(TFF)。我们确认工程的ECN可以在体外和体内分泌曲线融合的TFF,并且是非致病性的。我们观察到工程ECN对小鼠葡聚糖硫酸钠诱导的结肠炎的增强的保护作用,与粘膜愈合和免疫调节相关。这项工作为开发一个平台的基础,其中可以利用来自有益细菌的治疗性蛋白质基质的原位产生。

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