Cargando…
Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to infect hundred thousands of people every day worldwide. Since it is a novel virus, research continues to update the possible therapeutic targets when new evidence regarding COVID-1...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571447/ https://www.ncbi.nlm.nih.gov/pubmed/33091573 http://dx.doi.org/10.1016/j.freeradbiomed.2020.10.016 |
_version_ | 1783597174658957312 |
---|---|
author | Singh, Devendra Wasan, Himika Reeta, K.H. |
author_facet | Singh, Devendra Wasan, Himika Reeta, K.H. |
author_sort | Singh, Devendra |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to infect hundred thousands of people every day worldwide. Since it is a novel virus, research continues to update the possible therapeutic targets when new evidence regarding COVID-19 are gathered. This article presents an evidence-based hypothesis that activating the heme oxygenase-1 (HO-1) pathway is a potential target for COVID-19. Interferons (IFNs) have broad-spectrum antiviral activity including against SARS-CoV-2. Induction of HO-1 and increase in the heme catabolism end-product confer antiviral activity. IFN activation results in inhibition of viral replication in various viral infections. COVID-19 induced inflammation as well as acute respiratory distress syndrome (ARDS), and coagulopathies are now known major causes of mortality. A protective role of HO-1 induction in inflammation, inflammation-induced coagulation, and ARDS has been reported. Based on an association of HO-1 promoter polymorphisms and disease severity, we propose an evaluation of the status of these polymorphisms in COVID-19 patients who become severely ill. If an association is established, it might be helpful in identifying patients at high risk. Hence, we hypothesize that HO-1 pathway activation could be a therapeutic strategy against COVID-19 and associated complications. |
format | Online Article Text |
id | pubmed-7571447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75714472020-10-20 Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications Singh, Devendra Wasan, Himika Reeta, K.H. Free Radic Biol Med Hypothesis Paper Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to infect hundred thousands of people every day worldwide. Since it is a novel virus, research continues to update the possible therapeutic targets when new evidence regarding COVID-19 are gathered. This article presents an evidence-based hypothesis that activating the heme oxygenase-1 (HO-1) pathway is a potential target for COVID-19. Interferons (IFNs) have broad-spectrum antiviral activity including against SARS-CoV-2. Induction of HO-1 and increase in the heme catabolism end-product confer antiviral activity. IFN activation results in inhibition of viral replication in various viral infections. COVID-19 induced inflammation as well as acute respiratory distress syndrome (ARDS), and coagulopathies are now known major causes of mortality. A protective role of HO-1 induction in inflammation, inflammation-induced coagulation, and ARDS has been reported. Based on an association of HO-1 promoter polymorphisms and disease severity, we propose an evaluation of the status of these polymorphisms in COVID-19 patients who become severely ill. If an association is established, it might be helpful in identifying patients at high risk. Hence, we hypothesize that HO-1 pathway activation could be a therapeutic strategy against COVID-19 and associated complications. Elsevier Inc. 2020-12 2020-10-19 /pmc/articles/PMC7571447/ /pubmed/33091573 http://dx.doi.org/10.1016/j.freeradbiomed.2020.10.016 Text en © 2020 Elsevier Inc. All rights reserved. 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 | Hypothesis Paper Singh, Devendra Wasan, Himika Reeta, K.H. Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title | Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title_full | Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title_fullStr | Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title_full_unstemmed | Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title_short | Heme oxygenase-1 modulation: A potential therapeutic target for COVID-19 and associated complications |
title_sort | heme oxygenase-1 modulation: a potential therapeutic target for covid-19 and associated complications |
topic | Hypothesis Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571447/ https://www.ncbi.nlm.nih.gov/pubmed/33091573 http://dx.doi.org/10.1016/j.freeradbiomed.2020.10.016 |
work_keys_str_mv | AT singhdevendra hemeoxygenase1modulationapotentialtherapeutictargetforcovid19andassociatedcomplications AT wasanhimika hemeoxygenase1modulationapotentialtherapeutictargetforcovid19andassociatedcomplications AT reetakh hemeoxygenase1modulationapotentialtherapeutictargetforcovid19andassociatedcomplications |