细胞因子
细胞激素风暴
免疫系统
炎症
医学
肺
脂多糖
肿瘤坏死因子α
免疫学
肺炎
病理
内科学
疾病
2019年冠状病毒病(COVID-19)
传染病(医学专业)
作者
Tianyuan Ci,Yunbiao Xiong,Jinniu Zhang,Jing Zang,Nianping Feng
标识
DOI:10.1016/j.mtbio.2023.100684
摘要
Effectively controlling cytokine storm is important to reduce the mortality of severe pneumonia. In this work a bio-functional dead cell was engineered by one-time quick shock of live immune cells in liquid nitrogen, and the obtained immunosuppressive dead cell could server as both lung-targeting vehicle and cytokine absorption material. After loading the anti-inflammatory drugs of dexamethasone (DEX) and baicalin (BAI), the drug-loaded dead cell (DEX&BAI/Dead cell) could first passively target to the lung after intravenous administration and quickly release the drugs under high shearing stress of pulmonary capillaries, realizing drug enrichment in the lung. Then, the immunosuppressive dead cell acted as the camouflage of normal immune cells with various cytokine receptors exposing on their surface, to "capture" the cytokines and further reduce the state of inflammation. With above formulation design, a synergic anti-inflammatory effect between drugs and carrier could be achieved. In a lipopolysaccharide-induced pneumonia mice model, this system could calm down the cytokine storm with high efficacy and elongate the survival of mice.
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