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Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines

The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has highlighted the urgent need to rapidly develop therapeutic strategies for such emerging viruses without effective vaccines or drugs. Here, we report a decoy nanoparticle against COVID-19 through a powe...

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Autores principales: Rao, Lang, Xia, Shuai, Xu, Wei, Tian, Rui, Yu, Guocan, Gu, Chenjian, Pan, Pan, Meng, Qian-Fang, Cai, Xia, Qu, Di, Lu, Lu, Xie, Youhua, Jiang, Shibo, Chen, Xiaoyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959535/
https://www.ncbi.nlm.nih.gov/pubmed/33024017
http://dx.doi.org/10.1073/pnas.2014352117
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author Rao, Lang
Xia, Shuai
Xu, Wei
Tian, Rui
Yu, Guocan
Gu, Chenjian
Pan, Pan
Meng, Qian-Fang
Cai, Xia
Qu, Di
Lu, Lu
Xie, Youhua
Jiang, Shibo
Chen, Xiaoyuan
author_facet Rao, Lang
Xia, Shuai
Xu, Wei
Tian, Rui
Yu, Guocan
Gu, Chenjian
Pan, Pan
Meng, Qian-Fang
Cai, Xia
Qu, Di
Lu, Lu
Xie, Youhua
Jiang, Shibo
Chen, Xiaoyuan
author_sort Rao, Lang
collection PubMed
description The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has highlighted the urgent need to rapidly develop therapeutic strategies for such emerging viruses without effective vaccines or drugs. Here, we report a decoy nanoparticle against COVID-19 through a powerful two-step neutralization approach: virus neutralization in the first step followed by cytokine neutralization in the second step. The nanodecoy, made by fusing cellular membrane nanovesicles derived from human monocytes and genetically engineered cells stably expressing angiotensin converting enzyme II (ACE2) receptors, possesses an antigenic exterior the same as source cells. By competing with host cells for virus binding, these nanodecoys effectively protect host cells from the infection of pseudoviruses and authentic SARS-CoV-2. Moreover, relying on abundant cytokine receptors on the surface, the nanodecoys efficiently bind and neutralize inflammatory cytokines including interleukin 6 (IL-6) and granulocyte−macrophage colony-stimulating factor (GM-CSF), and significantly suppress immune disorder and lung injury in an acute pneumonia mouse model. Our work presents a simple, safe, and robust antiviral nanotechnology for ongoing COVID-19 and future potential epidemics.
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spelling pubmed-79595352021-03-22 Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines Rao, Lang Xia, Shuai Xu, Wei Tian, Rui Yu, Guocan Gu, Chenjian Pan, Pan Meng, Qian-Fang Cai, Xia Qu, Di Lu, Lu Xie, Youhua Jiang, Shibo Chen, Xiaoyuan Proc Natl Acad Sci U S A Physical Sciences The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has highlighted the urgent need to rapidly develop therapeutic strategies for such emerging viruses without effective vaccines or drugs. Here, we report a decoy nanoparticle against COVID-19 through a powerful two-step neutralization approach: virus neutralization in the first step followed by cytokine neutralization in the second step. The nanodecoy, made by fusing cellular membrane nanovesicles derived from human monocytes and genetically engineered cells stably expressing angiotensin converting enzyme II (ACE2) receptors, possesses an antigenic exterior the same as source cells. By competing with host cells for virus binding, these nanodecoys effectively protect host cells from the infection of pseudoviruses and authentic SARS-CoV-2. Moreover, relying on abundant cytokine receptors on the surface, the nanodecoys efficiently bind and neutralize inflammatory cytokines including interleukin 6 (IL-6) and granulocyte−macrophage colony-stimulating factor (GM-CSF), and significantly suppress immune disorder and lung injury in an acute pneumonia mouse model. Our work presents a simple, safe, and robust antiviral nanotechnology for ongoing COVID-19 and future potential epidemics. National Academy of Sciences 2020-11-03 2020-10-06 /pmc/articles/PMC7959535/ /pubmed/33024017 http://dx.doi.org/10.1073/pnas.2014352117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Physical Sciences
Rao, Lang
Xia, Shuai
Xu, Wei
Tian, Rui
Yu, Guocan
Gu, Chenjian
Pan, Pan
Meng, Qian-Fang
Cai, Xia
Qu, Di
Lu, Lu
Xie, Youhua
Jiang, Shibo
Chen, Xiaoyuan
Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title_full Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title_fullStr Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title_full_unstemmed Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title_short Decoy nanoparticles protect against COVID-19 by concurrently adsorbing viruses and inflammatory cytokines
title_sort decoy nanoparticles protect against covid-19 by concurrently adsorbing viruses and inflammatory cytokines
topic Physical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959535/
https://www.ncbi.nlm.nih.gov/pubmed/33024017
http://dx.doi.org/10.1073/pnas.2014352117
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