Bioengineered Neutrophils for Smart Response in Brain Infection Management

炎症 中枢神经系统 地塞米松 血脑屏障 金黄色葡萄球菌 抗生素 脑膜炎 医学 免疫学 趋化性 药理学 微生物学 细菌 生物 内科学 外科 受体 遗传学
作者
Anwei Zhou,Delian Kong,Xinyuan Zhou,Yao Liu,Yiping Zhang,Junrong Li,Yurui Xu,Xinghai Ning
出处
期刊:Advanced Materials [Wiley]
卷期号:36 (18): e2311661-e2311661 被引量:14
标识
DOI:10.1002/adma.202311661
摘要

Brain infections, frequently accompanied by significant inflammation, necessitate comprehensive therapeutic approaches targeting both infections and associated inflammation. A major impediment to such combined treatment is the blood-brain barrier (BBB), which significantly restricts therapeutic agents from achieving effective concentrations within the central nervous system. Here, a neutrophil-centric dual-responsive delivery system, coined "CellUs," is pioneered. This system is characterized by live neutrophils enveloping liposomes of dexamethasone, ceftriaxone, and oxygen-saturated perfluorocarbon (Lipo@D/C/P). CellUs is meticulously engineered to co-deliver antibiotics, anti-inflammatory agents, and oxygen, embodying a comprehensive strategy against brain infections. CellUs leverages the intrinsic abilities of neutrophils to navigate through BBB, accurately target infection sites, and synchronize the release of Lipo@D/C/P with local inflammatory signals. Notably, the incorporation of ultrasound-responsive perfluorocarbon within Lipo@D/C/P ensures the on-demand release of therapeutic agents at the afflicted regions. CellUs shows considerable promise in treating Staphylococcus aureus infections in mice with meningitis, particularly when combined with ultrasound treatments. It effectively penetrates BBB, significantly eliminates bacteria, reduces inflammation, and delivers oxygen to the affected brain tissue, resulting in a substantial improvement in survival rates. Consequently, CellUs harnesses the natural chemotactic properties of neutrophils and offers an innovative pathway to improve treatment effectiveness while minimizing adverse effects.
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