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Possible mechanisms of cholesterol elevation aggravating COVID-19
Importance: Despite the availability of a vaccine against the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), humans will have to live with this virus and the after-effects of the coronavirus disease 2019 (COVID-19) infection for a long time. Cholesterol plays an important role in the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436106/ https://www.ncbi.nlm.nih.gov/pubmed/34522180 http://dx.doi.org/10.7150/ijms.62021 |
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author | Tang, Yan Hu, Longtai Liu, Yi Zhou, Bangyi Qin, Xiaohuan Ye, Jujian Shen, Maoze Wu, Zhijian Zhang, Peidong |
author_facet | Tang, Yan Hu, Longtai Liu, Yi Zhou, Bangyi Qin, Xiaohuan Ye, Jujian Shen, Maoze Wu, Zhijian Zhang, Peidong |
author_sort | Tang, Yan |
collection | PubMed |
description | Importance: Despite the availability of a vaccine against the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), humans will have to live with this virus and the after-effects of the coronavirus disease 2019 (COVID-19) infection for a long time. Cholesterol plays an important role in the infection and prognosis of SARS-CoV-2, and the study of its mechanism is of great significance not only for the treatment of COVID-19 but also for research on generic antiviral drugs. Observations: Cholesterol promotes the development of atherosclerosis by activating NLR family pyrin domain containing 3 (NLRP3), and the resulting inflammatory environment indirectly contributes to COVID-19 infection and subsequent deterioration. In in vitro studies, membrane cholesterol increased the number of viral entry sites on the host cell membrane and the number of angiotensin-converting enzyme 2 (ACE2) receptors in the membrane fusion site. Previous studies have shown that the fusion protein of the virus interacts with cholesterol, and the spike protein of SARS-CoV-2 also requires cholesterol to enter the host cells. Cholesterol in blood interacts with the spike protein to promote the entry of spike cells, wherein the scavenger receptor class B type 1 (SR-B1) plays an important role. Because of the cardiovascular protective effects of lipid-lowering therapy and the additional anti-inflammatory effects of lipid-lowering drugs, it is currently recommended to continue lipid-lowering therapy for patients with COVID-19, but the safety of extremely low LDL-C is questionable. Conclusions and Relevance: Cholesterol can indirectly increase the susceptibility of patients to SARS-CoV-2 and increase the risk of death from COVID-19, which are mediated by NLRP3 and atherosclerotic plaques, respectively. Cholesterol present in the host cell membrane, virus, and blood may also directly participate in the virus cell entry process, but the specific mechanism still needs further study. Patients with COVID-19 are recommended to continue lipid-lowering therapy. |
format | Online Article Text |
id | pubmed-8436106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-84361062021-09-13 Possible mechanisms of cholesterol elevation aggravating COVID-19 Tang, Yan Hu, Longtai Liu, Yi Zhou, Bangyi Qin, Xiaohuan Ye, Jujian Shen, Maoze Wu, Zhijian Zhang, Peidong Int J Med Sci Review Importance: Despite the availability of a vaccine against the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), humans will have to live with this virus and the after-effects of the coronavirus disease 2019 (COVID-19) infection for a long time. Cholesterol plays an important role in the infection and prognosis of SARS-CoV-2, and the study of its mechanism is of great significance not only for the treatment of COVID-19 but also for research on generic antiviral drugs. Observations: Cholesterol promotes the development of atherosclerosis by activating NLR family pyrin domain containing 3 (NLRP3), and the resulting inflammatory environment indirectly contributes to COVID-19 infection and subsequent deterioration. In in vitro studies, membrane cholesterol increased the number of viral entry sites on the host cell membrane and the number of angiotensin-converting enzyme 2 (ACE2) receptors in the membrane fusion site. Previous studies have shown that the fusion protein of the virus interacts with cholesterol, and the spike protein of SARS-CoV-2 also requires cholesterol to enter the host cells. Cholesterol in blood interacts with the spike protein to promote the entry of spike cells, wherein the scavenger receptor class B type 1 (SR-B1) plays an important role. Because of the cardiovascular protective effects of lipid-lowering therapy and the additional anti-inflammatory effects of lipid-lowering drugs, it is currently recommended to continue lipid-lowering therapy for patients with COVID-19, but the safety of extremely low LDL-C is questionable. Conclusions and Relevance: Cholesterol can indirectly increase the susceptibility of patients to SARS-CoV-2 and increase the risk of death from COVID-19, which are mediated by NLRP3 and atherosclerotic plaques, respectively. Cholesterol present in the host cell membrane, virus, and blood may also directly participate in the virus cell entry process, but the specific mechanism still needs further study. Patients with COVID-19 are recommended to continue lipid-lowering therapy. Ivyspring International Publisher 2021-08-21 /pmc/articles/PMC8436106/ /pubmed/34522180 http://dx.doi.org/10.7150/ijms.62021 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Tang, Yan Hu, Longtai Liu, Yi Zhou, Bangyi Qin, Xiaohuan Ye, Jujian Shen, Maoze Wu, Zhijian Zhang, Peidong Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title | Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title_full | Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title_fullStr | Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title_full_unstemmed | Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title_short | Possible mechanisms of cholesterol elevation aggravating COVID-19 |
title_sort | possible mechanisms of cholesterol elevation aggravating covid-19 |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436106/ https://www.ncbi.nlm.nih.gov/pubmed/34522180 http://dx.doi.org/10.7150/ijms.62021 |
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