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COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy
SARS-CoV-2 infection is characterized by a protean clinical picture that can range from asymptomatic patients to life-threatening conditions. Severe COVID-19 patients often display a severe pulmonary involvement and develop neutrophilia, lymphopenia, and strikingly elevated levels of IL-6. There is...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366458/ https://www.ncbi.nlm.nih.gov/pubmed/32681497 http://dx.doi.org/10.1007/s12026-020-09145-5 |
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author | Perricone, Carlo Bartoloni, Elena Bursi, Roberto Cafaro, Giacomo Guidelli, Giacomo Maria Shoenfeld, Yehuda Gerli, Roberto |
author_facet | Perricone, Carlo Bartoloni, Elena Bursi, Roberto Cafaro, Giacomo Guidelli, Giacomo Maria Shoenfeld, Yehuda Gerli, Roberto |
author_sort | Perricone, Carlo |
collection | PubMed |
description | SARS-CoV-2 infection is characterized by a protean clinical picture that can range from asymptomatic patients to life-threatening conditions. Severe COVID-19 patients often display a severe pulmonary involvement and develop neutrophilia, lymphopenia, and strikingly elevated levels of IL-6. There is an over-exuberant cytokine release with hyperferritinemia leading to the idea that COVID-19 is part of the hyperferritinemic syndrome spectrum. Indeed, very high levels of ferritin can occur in other diseases including hemophagocytic lymphohistiocytosis, macrophage activation syndrome, adult-onset Still’s disease, catastrophic antiphospholipid syndrome and septic shock. Numerous studies have demonstrated the immunomodulatory effects of ferritin and its association with mortality and sustained inflammatory process. High levels of free iron are harmful in tissues, especially through the redox damage that can lead to fibrosis. Iron chelation represents a pillar in the treatment of iron overload. In addition, it was proven to have an anti-viral and anti-fibrotic activity. Herein, we analyse the pathogenic role of ferritin and iron during SARS-CoV-2 infection and propose iron depletion therapy as a novel therapeutic approach in the COVID-19 pandemic. |
format | Online Article Text |
id | pubmed-7366458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-73664582020-07-17 COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy Perricone, Carlo Bartoloni, Elena Bursi, Roberto Cafaro, Giacomo Guidelli, Giacomo Maria Shoenfeld, Yehuda Gerli, Roberto Immunol Res Interpretive Synthesis Review Article SARS-CoV-2 infection is characterized by a protean clinical picture that can range from asymptomatic patients to life-threatening conditions. Severe COVID-19 patients often display a severe pulmonary involvement and develop neutrophilia, lymphopenia, and strikingly elevated levels of IL-6. There is an over-exuberant cytokine release with hyperferritinemia leading to the idea that COVID-19 is part of the hyperferritinemic syndrome spectrum. Indeed, very high levels of ferritin can occur in other diseases including hemophagocytic lymphohistiocytosis, macrophage activation syndrome, adult-onset Still’s disease, catastrophic antiphospholipid syndrome and septic shock. Numerous studies have demonstrated the immunomodulatory effects of ferritin and its association with mortality and sustained inflammatory process. High levels of free iron are harmful in tissues, especially through the redox damage that can lead to fibrosis. Iron chelation represents a pillar in the treatment of iron overload. In addition, it was proven to have an anti-viral and anti-fibrotic activity. Herein, we analyse the pathogenic role of ferritin and iron during SARS-CoV-2 infection and propose iron depletion therapy as a novel therapeutic approach in the COVID-19 pandemic. Springer US 2020-07-17 2020 /pmc/articles/PMC7366458/ /pubmed/32681497 http://dx.doi.org/10.1007/s12026-020-09145-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Interpretive Synthesis Review Article Perricone, Carlo Bartoloni, Elena Bursi, Roberto Cafaro, Giacomo Guidelli, Giacomo Maria Shoenfeld, Yehuda Gerli, Roberto COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title | COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title_full | COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title_fullStr | COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title_full_unstemmed | COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title_short | COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
title_sort | covid-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy |
topic | Interpretive Synthesis Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366458/ https://www.ncbi.nlm.nih.gov/pubmed/32681497 http://dx.doi.org/10.1007/s12026-020-09145-5 |
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