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HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study
The SARS-CoV-2 pandemic has completely disrupted the health systems of the entire planet. From the earliest months, it became increasingly clear that in addition to affecting the upper airways and lungs, there were other organs that could be affected. Among these, the skin became a real “sentinel si...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392002/ https://www.ncbi.nlm.nih.gov/pubmed/34439887 http://dx.doi.org/10.3390/biom11081219 |
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author | Cazzato, Gerardo Colagrande, Anna Cimmino, Antonietta Cicco, Gerolamo Scarcella, Vincenza Sara Tarantino, Paola Lospalluti, Lucia Romita, Paolo Foti, Caterina Demarco, Aurora Sablone, Sara Candance, Pragnell Maria Victoria Cicco, Sebastiano Lettini, Teresa Ingravallo, Giuseppe Resta, Leonardo |
author_facet | Cazzato, Gerardo Colagrande, Anna Cimmino, Antonietta Cicco, Gerolamo Scarcella, Vincenza Sara Tarantino, Paola Lospalluti, Lucia Romita, Paolo Foti, Caterina Demarco, Aurora Sablone, Sara Candance, Pragnell Maria Victoria Cicco, Sebastiano Lettini, Teresa Ingravallo, Giuseppe Resta, Leonardo |
author_sort | Cazzato, Gerardo |
collection | PubMed |
description | The SARS-CoV-2 pandemic has completely disrupted the health systems of the entire planet. From the earliest months, it became increasingly clear that in addition to affecting the upper airways and lungs, there were other organs that could be affected. Among these, the skin became a real “sentinel signal” to be able to even suspect COVID-19. Background: this study deals with a little-explored issue for now: the study of skin immunopathology in SARS-CoV-2 positive subjects ascertained using the most reliable methods available. Methods: we used skin biopsy samples from SARS-CoV-2 positive and negative patients, studying morphology (Hematoxylin-Eosin), T lymphocyte population (CD4 and CD8), three markers such as HMGB-1, TIM-3 and HO-1 by immunohistochemistry. Results: although the presence of the CD4 and CD8 T population did not differ statistically significantly, we found greater activation and release of HMGB-1 in skin samples from SARS-CoV-2 positive patients, greater immunolabeling for TIM-3 at the level of CD4 and CD8 and a reduced expression of Heme oxygenase 1. Conclusions: these results support the possibility that there is immune deregulation in SARS-CoV-2 positive patients who develop skin manifestations of various kinds. |
format | Online Article Text |
id | pubmed-8392002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83920022021-08-28 HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study Cazzato, Gerardo Colagrande, Anna Cimmino, Antonietta Cicco, Gerolamo Scarcella, Vincenza Sara Tarantino, Paola Lospalluti, Lucia Romita, Paolo Foti, Caterina Demarco, Aurora Sablone, Sara Candance, Pragnell Maria Victoria Cicco, Sebastiano Lettini, Teresa Ingravallo, Giuseppe Resta, Leonardo Biomolecules Article The SARS-CoV-2 pandemic has completely disrupted the health systems of the entire planet. From the earliest months, it became increasingly clear that in addition to affecting the upper airways and lungs, there were other organs that could be affected. Among these, the skin became a real “sentinel signal” to be able to even suspect COVID-19. Background: this study deals with a little-explored issue for now: the study of skin immunopathology in SARS-CoV-2 positive subjects ascertained using the most reliable methods available. Methods: we used skin biopsy samples from SARS-CoV-2 positive and negative patients, studying morphology (Hematoxylin-Eosin), T lymphocyte population (CD4 and CD8), three markers such as HMGB-1, TIM-3 and HO-1 by immunohistochemistry. Results: although the presence of the CD4 and CD8 T population did not differ statistically significantly, we found greater activation and release of HMGB-1 in skin samples from SARS-CoV-2 positive patients, greater immunolabeling for TIM-3 at the level of CD4 and CD8 and a reduced expression of Heme oxygenase 1. Conclusions: these results support the possibility that there is immune deregulation in SARS-CoV-2 positive patients who develop skin manifestations of various kinds. MDPI 2021-08-16 /pmc/articles/PMC8392002/ /pubmed/34439887 http://dx.doi.org/10.3390/biom11081219 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cazzato, Gerardo Colagrande, Anna Cimmino, Antonietta Cicco, Gerolamo Scarcella, Vincenza Sara Tarantino, Paola Lospalluti, Lucia Romita, Paolo Foti, Caterina Demarco, Aurora Sablone, Sara Candance, Pragnell Maria Victoria Cicco, Sebastiano Lettini, Teresa Ingravallo, Giuseppe Resta, Leonardo HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title | HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title_full | HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title_fullStr | HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title_full_unstemmed | HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title_short | HMGB1-TIM3-HO1: A New Pathway of Inflammation in Skin of SARS-CoV-2 Patients? A Retrospective Pilot Study |
title_sort | hmgb1-tim3-ho1: a new pathway of inflammation in skin of sars-cov-2 patients? a retrospective pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392002/ https://www.ncbi.nlm.nih.gov/pubmed/34439887 http://dx.doi.org/10.3390/biom11081219 |
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