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The role of ibrutinib in COVID-19 hyperinflammation: A case report
Immune modulation in COVID-19 is emerging as an important therapeutic strategy as increasing evidence suggests that inflammatory pathways are implicated in lung damage. Bruton tyrosine kinase inhibitors (BTKi), such as ibrutinib, are commonly used to treat indolent B-cell neoplasms and chronic graft...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885681/ https://www.ncbi.nlm.nih.gov/pubmed/33607304 http://dx.doi.org/10.1016/j.ijid.2021.02.056 |
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author | Maynard, Suzanne Ros-Soto, Jose Chaidos, Aris Innes, Andrew Paleja, Krushika Mirvis, Eitan Buti, Noora Sharp, Harriet Palanicawandar, Renuka Milojkovic, Dragana |
author_facet | Maynard, Suzanne Ros-Soto, Jose Chaidos, Aris Innes, Andrew Paleja, Krushika Mirvis, Eitan Buti, Noora Sharp, Harriet Palanicawandar, Renuka Milojkovic, Dragana |
author_sort | Maynard, Suzanne |
collection | PubMed |
description | Immune modulation in COVID-19 is emerging as an important therapeutic strategy as increasing evidence suggests that inflammatory pathways are implicated in lung damage. Bruton tyrosine kinase inhibitors (BTKi), such as ibrutinib, are commonly used to treat indolent B-cell neoplasms and chronic graft-versus-host disease (GvHD). Given their potential to suppress pulmonary inflammatory cytokines and lessen acute lung injury, this could be applicable in the context of hospitalised COVID-19 patients. We describe an 81 year-old male receiving ibrutinib for Waldenstrom macroglobulinaemia (WM) who was hospitalised with COVID-19. On stopping the BTKi due to concerns of additional immunosuppression, he required non-invasive ventilation (NIV) in the intensive care unit (ICU) and demonstrated prompt clinical recovery when ibrutinib was reinstated. Continuing ibrutinib in patients with COVID-19 may be advantageous given its immunomodulatory properties and withdrawal of ibrutinib therapy may be detrimental. Further evidence is required to explore the potential therapeutic impact of BTKis and other immunomodulatory agents on the clinical course of COVID-19 as is currently being carried out in a number of clinical trials. |
format | Online Article Text |
id | pubmed-7885681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78856812021-02-16 The role of ibrutinib in COVID-19 hyperinflammation: A case report Maynard, Suzanne Ros-Soto, Jose Chaidos, Aris Innes, Andrew Paleja, Krushika Mirvis, Eitan Buti, Noora Sharp, Harriet Palanicawandar, Renuka Milojkovic, Dragana Int J Infect Dis Case Report Immune modulation in COVID-19 is emerging as an important therapeutic strategy as increasing evidence suggests that inflammatory pathways are implicated in lung damage. Bruton tyrosine kinase inhibitors (BTKi), such as ibrutinib, are commonly used to treat indolent B-cell neoplasms and chronic graft-versus-host disease (GvHD). Given their potential to suppress pulmonary inflammatory cytokines and lessen acute lung injury, this could be applicable in the context of hospitalised COVID-19 patients. We describe an 81 year-old male receiving ibrutinib for Waldenstrom macroglobulinaemia (WM) who was hospitalised with COVID-19. On stopping the BTKi due to concerns of additional immunosuppression, he required non-invasive ventilation (NIV) in the intensive care unit (ICU) and demonstrated prompt clinical recovery when ibrutinib was reinstated. Continuing ibrutinib in patients with COVID-19 may be advantageous given its immunomodulatory properties and withdrawal of ibrutinib therapy may be detrimental. Further evidence is required to explore the potential therapeutic impact of BTKis and other immunomodulatory agents on the clinical course of COVID-19 as is currently being carried out in a number of clinical trials. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2021-04 2021-02-16 /pmc/articles/PMC7885681/ /pubmed/33607304 http://dx.doi.org/10.1016/j.ijid.2021.02.056 Text en Crown Copyright © 2021 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 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 | Case Report Maynard, Suzanne Ros-Soto, Jose Chaidos, Aris Innes, Andrew Paleja, Krushika Mirvis, Eitan Buti, Noora Sharp, Harriet Palanicawandar, Renuka Milojkovic, Dragana The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title | The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title_full | The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title_fullStr | The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title_full_unstemmed | The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title_short | The role of ibrutinib in COVID-19 hyperinflammation: A case report |
title_sort | role of ibrutinib in covid-19 hyperinflammation: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885681/ https://www.ncbi.nlm.nih.gov/pubmed/33607304 http://dx.doi.org/10.1016/j.ijid.2021.02.056 |
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