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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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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. |
format | Online Article Text |
id | pubmed-7959535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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