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HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association
Systemic sclerosis (SSc) is an autoimmune disease characterized by vasculopathy, excessive extracellular matrix deposition, and fibrosis of the skin and internal organs. Several infectious agents, including human herpesvirus-6 (HHV-6), have been suggested as possible triggering factors, but a direct...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022325/ https://www.ncbi.nlm.nih.gov/pubmed/31878218 http://dx.doi.org/10.3390/microorganisms8010039 |
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author | Caselli, Elisabetta Soffritti, Irene D’Accolti, Maria Bortolotti, Daria Rizzo, Roberta Sighinolfi, Gianluca Giuggioli, Dilia Ferri, Clodoveo |
author_facet | Caselli, Elisabetta Soffritti, Irene D’Accolti, Maria Bortolotti, Daria Rizzo, Roberta Sighinolfi, Gianluca Giuggioli, Dilia Ferri, Clodoveo |
author_sort | Caselli, Elisabetta |
collection | PubMed |
description | Systemic sclerosis (SSc) is an autoimmune disease characterized by vasculopathy, excessive extracellular matrix deposition, and fibrosis of the skin and internal organs. Several infectious agents, including human herpesvirus-6 (HHV-6), have been suggested as possible triggering factors, but a direct association is still missing. We characterized 26 SSc patients for the presence of HHV-6 in tissues and blood, the anti-HHV-6 response, HLA-G plasma levels, and KIR typing. Given the prominent role of endothelial cells (EC) in SSc pathogenesis, along with HHV-6 tropism for EC, we also investigated the expression of pro-fibrosis factors in HHV-6 infected EC. Results showed the presence of HHV-6A in skin biopsies, and an increased virus load was associated with disease severity and poor natural killer (NK) response against the virus, particularly in subjects exhibiting a KIR2 phenotype. HLA-G plasma levels were significantly higher in HHV-6A/B-KIR2 positive SSc patients and in vitro HHV-6A infection-induced pro-fibrosis factors expression in EC, supporting its role in the development of the fibrosing process. Our data suggest an association between virus infection/reactivation and disease, opening the way to future studies to understand the mechanisms by which HHV-6A might contribute to the multifactorial pathogenesis of SSc. |
format | Online Article Text |
id | pubmed-7022325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70223252020-03-09 HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association Caselli, Elisabetta Soffritti, Irene D’Accolti, Maria Bortolotti, Daria Rizzo, Roberta Sighinolfi, Gianluca Giuggioli, Dilia Ferri, Clodoveo Microorganisms Article Systemic sclerosis (SSc) is an autoimmune disease characterized by vasculopathy, excessive extracellular matrix deposition, and fibrosis of the skin and internal organs. Several infectious agents, including human herpesvirus-6 (HHV-6), have been suggested as possible triggering factors, but a direct association is still missing. We characterized 26 SSc patients for the presence of HHV-6 in tissues and blood, the anti-HHV-6 response, HLA-G plasma levels, and KIR typing. Given the prominent role of endothelial cells (EC) in SSc pathogenesis, along with HHV-6 tropism for EC, we also investigated the expression of pro-fibrosis factors in HHV-6 infected EC. Results showed the presence of HHV-6A in skin biopsies, and an increased virus load was associated with disease severity and poor natural killer (NK) response against the virus, particularly in subjects exhibiting a KIR2 phenotype. HLA-G plasma levels were significantly higher in HHV-6A/B-KIR2 positive SSc patients and in vitro HHV-6A infection-induced pro-fibrosis factors expression in EC, supporting its role in the development of the fibrosing process. Our data suggest an association between virus infection/reactivation and disease, opening the way to future studies to understand the mechanisms by which HHV-6A might contribute to the multifactorial pathogenesis of SSc. MDPI 2019-12-24 /pmc/articles/PMC7022325/ /pubmed/31878218 http://dx.doi.org/10.3390/microorganisms8010039 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Caselli, Elisabetta Soffritti, Irene D’Accolti, Maria Bortolotti, Daria Rizzo, Roberta Sighinolfi, Gianluca Giuggioli, Dilia Ferri, Clodoveo HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title | HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title_full | HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title_fullStr | HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title_full_unstemmed | HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title_short | HHV-6A Infection and Systemic Sclerosis: Clues of a Possible Association |
title_sort | hhv-6a infection and systemic sclerosis: clues of a possible association |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022325/ https://www.ncbi.nlm.nih.gov/pubmed/31878218 http://dx.doi.org/10.3390/microorganisms8010039 |
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