细胞激素风暴
促炎细胞因子
医学
脾脏
免疫系统
细胞因子
吸入
免疫学
肺
肺炎
呼吸道
药理学
炎症
呼吸系统
2019年冠状病毒病(COVID-19)
传染病(医学专业)
病理
疾病
内科学
解剖
作者
Zhen Wang,Lei Xiang,Feng Lin,Zhengwei Cai,Huitong Ruan,Juan Wang,Jing Liang,Fei Wang,Min Lü,Wenguo Cui
出处
期刊:Matter
[Elsevier]
日期:2021-10-22
卷期号:5 (1): 336-362
被引量:47
标识
DOI:10.1016/j.matt.2021.09.022
摘要
The SARS-CoV-2 pandemic spread worldwide unabated. However, achieving protection from the virus in the whole respiratory tract, avoiding blood dissemination, and calming the subsequent cytokine storm remains a major challenge. Here, we develop an inhaled microfluidic microsphere using dual camouflaged methacrylate hyaluronic acid hydrogel microspheres with a genetically engineered membrane from angiotensin-converting enzyme II (ACE2) receptor-overexpressing cells and macrophages. By timely competing with the virus for ACE2 binding, the inhaled microspheres significantly reduce SARS-CoV-2 infective effectiveness over the whole course of the respiratory system in vitro and in vivo. Moreover, the inhaled microspheres efficiently neutralize proinflammatory cytokines, cause an alternative landscape of lung-infiltrated immune cells, and alleviate hyperinflammation of lymph nodes and spleen. In an acute pneumonia model, the inhaled microspheres show significant therapeutic efficacy by regulation of the multisystem inflammatory syndrome and reduce acute mortality, suggesting a powerful synergic strategy for the treatment of patients with severe COVID-19 via non-invasive administration.
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