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A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling

Hyperinflammation plays an important role in severe and critical COVID-19. Using inconsistent criteria, many researchers define hyperinflammation as a form of very severe inflammation with cytokine storm. Therefore, COVID-19 patients are treated with anti-inflammatory drugs. These drugs appear to be...

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Autores principales: Hasan, Djo, Shono, Atsuko, van Kalken, Coenraad K., van der Spek, Peter J., Krenning, Eric P., Kotani, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578920/
https://www.ncbi.nlm.nih.gov/pubmed/34757513
http://dx.doi.org/10.1007/s11302-021-09814-6
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author Hasan, Djo
Shono, Atsuko
van Kalken, Coenraad K.
van der Spek, Peter J.
Krenning, Eric P.
Kotani, Toru
author_facet Hasan, Djo
Shono, Atsuko
van Kalken, Coenraad K.
van der Spek, Peter J.
Krenning, Eric P.
Kotani, Toru
author_sort Hasan, Djo
collection PubMed
description Hyperinflammation plays an important role in severe and critical COVID-19. Using inconsistent criteria, many researchers define hyperinflammation as a form of very severe inflammation with cytokine storm. Therefore, COVID-19 patients are treated with anti-inflammatory drugs. These drugs appear to be less efficacious than expected and are sometimes accompanied by serious adverse effects. SARS-CoV-2 promotes cellular ATP release. Increased levels of extracellular ATP activate the purinergic receptors of the immune cells initiating the physiologic pro-inflammatory immune response. Persisting viral infection drives the ATP release even further leading to the activation of the P2X7 purinergic receptors (P2X7Rs) and a severe yet physiologic inflammation. Disease progression promotes prolonged vigorous activation of the P2X7R causing cell death and uncontrolled ATP release leading to cytokine storm and desensitisation of all other purinergic receptors of the immune cells. This results in immune paralysis with co-infections or secondary infections. We refer to this pathologic condition as hyperinflammation. The readily available and affordable P2X7R antagonist lidocaine can abrogate hyperinflammation and restore the normal immune function. The issue is that the half-maximal effective concentration for P2X7R inhibition of lidocaine is much higher than the maximal tolerable plasma concentration where adverse effects start to develop. To overcome this, we selectively inhibit the P2X7Rs of the immune cells of the lymphatic system inducing clonal expansion of Tregs in local lymph nodes. Subsequently, these Tregs migrate throughout the body exerting anti-inflammatory activities suppressing systemic and (distant) local hyperinflammation. We illustrate this with six critically ill COVID-19 patients treated with lidocaine.
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spelling pubmed-85789202021-11-10 A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling Hasan, Djo Shono, Atsuko van Kalken, Coenraad K. van der Spek, Peter J. Krenning, Eric P. Kotani, Toru Purinergic Signal Commentary Hyperinflammation plays an important role in severe and critical COVID-19. Using inconsistent criteria, many researchers define hyperinflammation as a form of very severe inflammation with cytokine storm. Therefore, COVID-19 patients are treated with anti-inflammatory drugs. These drugs appear to be less efficacious than expected and are sometimes accompanied by serious adverse effects. SARS-CoV-2 promotes cellular ATP release. Increased levels of extracellular ATP activate the purinergic receptors of the immune cells initiating the physiologic pro-inflammatory immune response. Persisting viral infection drives the ATP release even further leading to the activation of the P2X7 purinergic receptors (P2X7Rs) and a severe yet physiologic inflammation. Disease progression promotes prolonged vigorous activation of the P2X7R causing cell death and uncontrolled ATP release leading to cytokine storm and desensitisation of all other purinergic receptors of the immune cells. This results in immune paralysis with co-infections or secondary infections. We refer to this pathologic condition as hyperinflammation. The readily available and affordable P2X7R antagonist lidocaine can abrogate hyperinflammation and restore the normal immune function. The issue is that the half-maximal effective concentration for P2X7R inhibition of lidocaine is much higher than the maximal tolerable plasma concentration where adverse effects start to develop. To overcome this, we selectively inhibit the P2X7Rs of the immune cells of the lymphatic system inducing clonal expansion of Tregs in local lymph nodes. Subsequently, these Tregs migrate throughout the body exerting anti-inflammatory activities suppressing systemic and (distant) local hyperinflammation. We illustrate this with six critically ill COVID-19 patients treated with lidocaine. Springer Netherlands 2021-11-10 2022-03 /pmc/articles/PMC8578920/ /pubmed/34757513 http://dx.doi.org/10.1007/s11302-021-09814-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Hasan, Djo
Shono, Atsuko
van Kalken, Coenraad K.
van der Spek, Peter J.
Krenning, Eric P.
Kotani, Toru
A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title_full A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title_fullStr A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title_full_unstemmed A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title_short A novel definition and treatment of hyperinflammation in COVID-19 based on purinergic signalling
title_sort novel definition and treatment of hyperinflammation in covid-19 based on purinergic signalling
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578920/
https://www.ncbi.nlm.nih.gov/pubmed/34757513
http://dx.doi.org/10.1007/s11302-021-09814-6
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