The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis
Autoimmune diseases are a diverse group of chronic disorders and affect a multitude of organs and systems. However, the existence of common pathophysiological mechanisms is hypothesized and reports of shared risk are emerging as well. In this regard, patients with multiple sclerosis (MS) have been s...
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Frontiers Media S.A.
2018-02-01
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Online Access: | http://journal.frontiersin.org/article/10.3389/fimmu.2018.00311/full |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Simona Perga Simona Perga Simona Perga Serena Martire Serena Martire Francesca Montarolo Francesca Montarolo Francesca Montarolo Ilaria Giordani Michela Spadaro Michela Spadaro Gabriele Bono Gabriele Bono Stefania Corvisieri Ilaria Messuti Giancarlo Panzica Giancarlo Panzica Fabio Orlandi Antonio Bertolotto Antonio Bertolotto |
spellingShingle |
Simona Perga Simona Perga Simona Perga Serena Martire Serena Martire Francesca Montarolo Francesca Montarolo Francesca Montarolo Ilaria Giordani Michela Spadaro Michela Spadaro Gabriele Bono Gabriele Bono Stefania Corvisieri Ilaria Messuti Giancarlo Panzica Giancarlo Panzica Fabio Orlandi Antonio Bertolotto Antonio Bertolotto The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis Frontiers in Immunology multiple sclerosis Hashimoto’s thyroiditis gene expression 25-hydroxy vitamin D regulatory T cells |
author_facet |
Simona Perga Simona Perga Simona Perga Serena Martire Serena Martire Francesca Montarolo Francesca Montarolo Francesca Montarolo Ilaria Giordani Michela Spadaro Michela Spadaro Gabriele Bono Gabriele Bono Stefania Corvisieri Ilaria Messuti Giancarlo Panzica Giancarlo Panzica Fabio Orlandi Antonio Bertolotto Antonio Bertolotto |
author_sort |
Simona Perga |
title |
The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis |
title_short |
The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis |
title_full |
The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis |
title_fullStr |
The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis |
title_full_unstemmed |
The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s Thyroiditis |
title_sort |
footprints of poly-autoimmunity: evidence for common biological factors involved in multiple sclerosis and hashimoto’s thyroiditis |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2018-02-01 |
description |
Autoimmune diseases are a diverse group of chronic disorders and affect a multitude of organs and systems. However, the existence of common pathophysiological mechanisms is hypothesized and reports of shared risk are emerging as well. In this regard, patients with multiple sclerosis (MS) have been shown to have an increased susceptibility to develop chronic autoimmune thyroid diseases, in particular Hashimoto’s thyroiditis (HT), suggesting an autoimmune predisposition. However, studies comparing such different pathologies of autoimmune origin are still missing till date. In the present study, we sought to investigate mechanisms which may lead to the frequent coexistence of MS and HT by analyzing several factors related to the pathogenesis of MS and HT in patients affected by one or both diseases, as well as in healthy donors. In particular, we analyzed peripheral blood mononuclear cell gene-expression levels of common candidate genes such as TNFAIP3, NR4A family, BACH2, FOXP3, and PDCD5, in addition to the regulatory T cell (Treg) percentage and the 25-hydroxy vitamin D serum levels. Our findings support the plausibility of the existence of common deregulated mechanisms shared by MS and HT, such as BACH2/PDCD5-FOXP3 pathways and Tregs. Although the biological implications of these data need to be further investigated, we have highlighted the relevance of studies comparing different autoimmune pathologies for the understanding of the core concepts of autoimmunity. |
topic |
multiple sclerosis Hashimoto’s thyroiditis gene expression 25-hydroxy vitamin D regulatory T cells |
url |
http://journal.frontiersin.org/article/10.3389/fimmu.2018.00311/full |
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doaj-b06c35d4197d41c892023bd134f7183e2020-11-25T00:30:57ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-02-01910.3389/fimmu.2018.00311326254The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto’s ThyroiditisSimona Perga0Simona Perga1Simona Perga2Serena Martire3Serena Martire4Francesca Montarolo5Francesca Montarolo6Francesca Montarolo7Ilaria Giordani8Michela Spadaro9Michela Spadaro10Gabriele Bono11Gabriele Bono12Stefania Corvisieri13Ilaria Messuti14Giancarlo Panzica15Giancarlo Panzica16Fabio Orlandi17Antonio Bertolotto18Antonio Bertolotto19Neuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalyDepartment of Neuroscience Rita Levi Montalcini, University of Turin, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalyDepartment of Neuroscience Rita Levi Montalcini, University of Turin, Turin, ItalySCDU Endocrinology and Metabolism, Humanitas Gradenigo Hospital, Department of Oncology, University of Turin, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalySCDU Endocrinology and Metabolism, Humanitas Gradenigo Hospital, Department of Oncology, University of Turin, Turin, ItalySCDU Endocrinology and Metabolism, Humanitas Gradenigo Hospital, Department of Oncology, University of Turin, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyDepartment of Neuroscience Rita Levi Montalcini, University of Turin, Turin, ItalySCDU Endocrinology and Metabolism, Humanitas Gradenigo Hospital, Department of Oncology, University of Turin, Turin, ItalyNeuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Turin, ItalyRegional Reference Centre for Multiple Sclerosis (CReSM), University Hospital S. Luigi Gonzaga, Orbassano, Turin, ItalyAutoimmune diseases are a diverse group of chronic disorders and affect a multitude of organs and systems. However, the existence of common pathophysiological mechanisms is hypothesized and reports of shared risk are emerging as well. In this regard, patients with multiple sclerosis (MS) have been shown to have an increased susceptibility to develop chronic autoimmune thyroid diseases, in particular Hashimoto’s thyroiditis (HT), suggesting an autoimmune predisposition. However, studies comparing such different pathologies of autoimmune origin are still missing till date. In the present study, we sought to investigate mechanisms which may lead to the frequent coexistence of MS and HT by analyzing several factors related to the pathogenesis of MS and HT in patients affected by one or both diseases, as well as in healthy donors. In particular, we analyzed peripheral blood mononuclear cell gene-expression levels of common candidate genes such as TNFAIP3, NR4A family, BACH2, FOXP3, and PDCD5, in addition to the regulatory T cell (Treg) percentage and the 25-hydroxy vitamin D serum levels. Our findings support the plausibility of the existence of common deregulated mechanisms shared by MS and HT, such as BACH2/PDCD5-FOXP3 pathways and Tregs. Although the biological implications of these data need to be further investigated, we have highlighted the relevance of studies comparing different autoimmune pathologies for the understanding of the core concepts of autoimmunity.http://journal.frontiersin.org/article/10.3389/fimmu.2018.00311/fullmultiple sclerosisHashimoto’s thyroiditisgene expression25-hydroxy vitamin Dregulatory T cells |