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用于气管内中和新冠病毒并平息细胞因子风暴的吸入式工程化血管紧张素转换酶2微流体微球

Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm.

作者信息

Wang Zhen, Xiang Lei, Lin Feng, Cai Zhengwei, Ruan Huitong, Wang Juan, Liang Jing, Wang Fei, Lu Min, Cui Wenguo

机构信息

Department of Orthopaedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

出版信息

Matter. 2022 Jan 5;5(1):336-362. doi: 10.1016/j.matt.2021.09.022. Epub 2021 Oct 19.

Abstract

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 and . 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.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行在全球范围内持续蔓延。然而,在整个呼吸道实现对该病毒的防护、避免血液传播以及平息随后的细胞因子风暴仍然是一项重大挑战。在此,我们开发了一种吸入式微流控微球,其采用了双重伪装的甲基丙烯酸酯透明质酸水凝胶微球,并带有来自过表达血管紧张素转换酶2(ACE2)受体的细胞和巨噬细胞的基因工程膜。通过及时与病毒竞争ACE2结合位点,吸入式微球在呼吸系统的整个过程中显著降低了SARS-CoV-2的感染效力。此外,吸入式微球有效地中和促炎细胞因子,导致肺浸润免疫细胞呈现不同格局,并减轻淋巴结和脾脏的过度炎症。在急性肺炎模型中,吸入式微球通过调节多系统炎症综合征显示出显著的治疗效果,并降低急性死亡率,这表明通过非侵入性给药治疗重症2019冠状病毒病患者是一种强大的协同策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b3/8524658/a3003ef033db/fx1_lrg.jpg

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