Cargando…

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

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 camouflag...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Zhen, Xiang, Lei, Lin, Feng, Cai, Zhengwei, Ruan, Huitong, Wang, Juan, Liang, Jing, Wang, Fei, Lu, Min, Cui, Wenguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524658/
https://www.ncbi.nlm.nih.gov/pubmed/34693277
http://dx.doi.org/10.1016/j.matt.2021.09.022
_version_ 1784585522528649216
author Wang, Zhen
Xiang, Lei
Lin, Feng
Cai, Zhengwei
Ruan, Huitong
Wang, Juan
Liang, Jing
Wang, Fei
Lu, Min
Cui, Wenguo
author_facet Wang, Zhen
Xiang, Lei
Lin, Feng
Cai, Zhengwei
Ruan, Huitong
Wang, Juan
Liang, Jing
Wang, Fei
Lu, Min
Cui, Wenguo
author_sort Wang, Zhen
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8524658
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-85246582021-10-20 Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm Wang, Zhen Xiang, Lei Lin, Feng Cai, Zhengwei Ruan, Huitong Wang, Juan Liang, Jing Wang, Fei Lu, Min Cui, Wenguo Matter Article 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. Elsevier Inc. 2022-01-05 2021-10-19 /pmc/articles/PMC8524658/ /pubmed/34693277 http://dx.doi.org/10.1016/j.matt.2021.09.022 Text en © 2021 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wang, Zhen
Xiang, Lei
Lin, Feng
Cai, Zhengwei
Ruan, Huitong
Wang, Juan
Liang, Jing
Wang, Fei
Lu, Min
Cui, Wenguo
Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title_full Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title_fullStr Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title_full_unstemmed Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title_short Inhaled ACE2-engineered microfluidic microsphere for intratracheal neutralization of COVID-19 and calming of the cytokine storm
title_sort inhaled ace2-engineered microfluidic microsphere for intratracheal neutralization of covid-19 and calming of the cytokine storm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524658/
https://www.ncbi.nlm.nih.gov/pubmed/34693277
http://dx.doi.org/10.1016/j.matt.2021.09.022
work_keys_str_mv AT wangzhen inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT xianglei inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT linfeng inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT caizhengwei inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT ruanhuitong inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT wangjuan inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT liangjing inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT wangfei inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT lumin inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm
AT cuiwenguo inhaledace2engineeredmicrofluidicmicrosphereforintratrachealneutralizationofcovid19andcalmingofthecytokinestorm