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Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review
Coronavirus disease 2019 (COVID-19) is first detected in December 2019 in Wuhan, China which is a new pandemic caused by SARS-COV-2 that has greatly affected the whole world. Bruton tyrosine kinase (BTK) inhibitors are drugs that are used for the management of cancer, and are being repurposed for CO...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318668/ https://www.ncbi.nlm.nih.gov/pubmed/34345815 http://dx.doi.org/10.1016/j.metop.2021.100116 |
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author | Kifle, Zemene Demelash |
author_facet | Kifle, Zemene Demelash |
author_sort | Kifle, Zemene Demelash |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is first detected in December 2019 in Wuhan, China which is a new pandemic caused by SARS-COV-2 that has greatly affected the whole world. Bruton tyrosine kinase (BTK) inhibitors are drugs that are used for the management of cancer, and are being repurposed for COVID-19. BTK regulates macrophage and B cell activation, development, survival, and signaling. Inhibition of BTK has revealed an ameliorative effect on lung injury in patients with severe COVID-19. Thus, this review aimed to summarize evidence regarding the role of Bruton tyrosine kinase inhibitors against COVID-19. To include findings from diverse studies, publications related to BTK inhibitors and Covid-19 were searched from the databases such as SCOPUS, Web of Science, Medline, Google Scholar, PubMed, and Elsevier, using English key terms. Both experimental and clinical studies suggest that targeting excessive host inflammation with a BTK inhibitor is a potential therapeutic strategy in the treatment of patients with severe COVID-19. Currently, BTK inhibitors such as ibrutinib and acalabrutinib have shown a protective effect against pulmonary injury in a small series group of COVID-19 infected patients. Small molecule inhibitors like BTK inhibitors, targeting a wide range of pro-inflammatory singling pathways, may a key role in the management of COVID-19. |
format | Online Article Text |
id | pubmed-8318668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83186682021-07-29 Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review Kifle, Zemene Demelash Metabol Open Articles from the Vaccines, Immune Response, Therapeutic Interventions and COVID-19 Special Issue Coronavirus disease 2019 (COVID-19) is first detected in December 2019 in Wuhan, China which is a new pandemic caused by SARS-COV-2 that has greatly affected the whole world. Bruton tyrosine kinase (BTK) inhibitors are drugs that are used for the management of cancer, and are being repurposed for COVID-19. BTK regulates macrophage and B cell activation, development, survival, and signaling. Inhibition of BTK has revealed an ameliorative effect on lung injury in patients with severe COVID-19. Thus, this review aimed to summarize evidence regarding the role of Bruton tyrosine kinase inhibitors against COVID-19. To include findings from diverse studies, publications related to BTK inhibitors and Covid-19 were searched from the databases such as SCOPUS, Web of Science, Medline, Google Scholar, PubMed, and Elsevier, using English key terms. Both experimental and clinical studies suggest that targeting excessive host inflammation with a BTK inhibitor is a potential therapeutic strategy in the treatment of patients with severe COVID-19. Currently, BTK inhibitors such as ibrutinib and acalabrutinib have shown a protective effect against pulmonary injury in a small series group of COVID-19 infected patients. Small molecule inhibitors like BTK inhibitors, targeting a wide range of pro-inflammatory singling pathways, may a key role in the management of COVID-19. Elsevier 2021-07-29 /pmc/articles/PMC8318668/ /pubmed/34345815 http://dx.doi.org/10.1016/j.metop.2021.100116 Text en © 2021 The Author https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles from the Vaccines, Immune Response, Therapeutic Interventions and COVID-19 Special Issue Kifle, Zemene Demelash Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title | Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title_full | Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title_fullStr | Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title_full_unstemmed | Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title_short | Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review |
title_sort | bruton tyrosine kinase inhibitors as potential therapeutic agents for covid-19: a review |
topic | Articles from the Vaccines, Immune Response, Therapeutic Interventions and COVID-19 Special Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318668/ https://www.ncbi.nlm.nih.gov/pubmed/34345815 http://dx.doi.org/10.1016/j.metop.2021.100116 |
work_keys_str_mv | AT kiflezemenedemelash brutontyrosinekinaseinhibitorsaspotentialtherapeuticagentsforcovid19areview |