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Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2

Both immune reconstitution inflammatory syndrome (IRIS) and severe coronavirus disease 2019 (COVID-19) are marked by hyperinflammation as a consequence of dysfunction in myeloid cells and increased production of proinflammatory cytokines. Although these features are common to both diseases, their ph...

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Autores principales: Garcia-Carretero, Rafael, Vazquez-Gomez, Oscar, Ordoñez-Garcia, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665849/
https://www.ncbi.nlm.nih.gov/pubmed/34912622
http://dx.doi.org/10.7759/cureus.19481
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author Garcia-Carretero, Rafael
Vazquez-Gomez, Oscar
Ordoñez-Garcia, Maria
author_facet Garcia-Carretero, Rafael
Vazquez-Gomez, Oscar
Ordoñez-Garcia, Maria
author_sort Garcia-Carretero, Rafael
collection PubMed
description Both immune reconstitution inflammatory syndrome (IRIS) and severe coronavirus disease 2019 (COVID-19) are marked by hyperinflammation as a consequence of dysfunction in myeloid cells and increased production of proinflammatory cytokines. Although these features are common to both diseases, their physiopathology remains unclear. Here we report the case of a 63-year-old woman admitted for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In her clinical course, she developed acute respiratory distress syndrome, probably triggered by the use of granulocyte colony-stimulating factor (G-CSF). We hypothesize that G-CSF unmasked IRIS.
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spelling pubmed-86658492021-12-14 Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2 Garcia-Carretero, Rafael Vazquez-Gomez, Oscar Ordoñez-Garcia, Maria Cureus Internal Medicine Both immune reconstitution inflammatory syndrome (IRIS) and severe coronavirus disease 2019 (COVID-19) are marked by hyperinflammation as a consequence of dysfunction in myeloid cells and increased production of proinflammatory cytokines. Although these features are common to both diseases, their physiopathology remains unclear. Here we report the case of a 63-year-old woman admitted for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In her clinical course, she developed acute respiratory distress syndrome, probably triggered by the use of granulocyte colony-stimulating factor (G-CSF). We hypothesize that G-CSF unmasked IRIS. Cureus 2021-11-11 /pmc/articles/PMC8665849/ /pubmed/34912622 http://dx.doi.org/10.7759/cureus.19481 Text en Copyright © 2021, Garcia-Carretero et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Garcia-Carretero, Rafael
Vazquez-Gomez, Oscar
Ordoñez-Garcia, Maria
Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title_full Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title_fullStr Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title_full_unstemmed Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title_short Delayed Immune Reconstitution Inflammatory Syndrome in an Immunosuppressed Patient With SARS-CoV-2
title_sort delayed immune reconstitution inflammatory syndrome in an immunosuppressed patient with sars-cov-2
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665849/
https://www.ncbi.nlm.nih.gov/pubmed/34912622
http://dx.doi.org/10.7759/cureus.19481
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