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Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease

Gorham-Stout disease (GSD) is a very rare syndrome displaying excessive bone erosion and vascular lesion. Due to the rarity of the disease and to the limited studies, its etiopathogenesis is not entirely known. The involvement of immune system in the progressive osteolysis was recently suggested. In...

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Autores principales: Rossi, Michela, Rana, Ippolita, Buonuomo, Paola Sabrina, Battafarano, Giulia, De Martino, Viviana, D’Agostini, Matteo, Porzio, Ottavia, Cipriani, Cristiana, Minisola, Salvatore, De Vito, Rita, Vecchio, Davide, Gonfiantini, Michaela Veronika, Jenkner, Alessandro, Bartuli, Andrea, Del Fattore, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430039/
https://www.ncbi.nlm.nih.gov/pubmed/34513837
http://dx.doi.org/10.3389/fcell.2021.706596
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author Rossi, Michela
Rana, Ippolita
Buonuomo, Paola Sabrina
Battafarano, Giulia
De Martino, Viviana
D’Agostini, Matteo
Porzio, Ottavia
Cipriani, Cristiana
Minisola, Salvatore
De Vito, Rita
Vecchio, Davide
Gonfiantini, Michaela Veronika
Jenkner, Alessandro
Bartuli, Andrea
Del Fattore, Andrea
author_facet Rossi, Michela
Rana, Ippolita
Buonuomo, Paola Sabrina
Battafarano, Giulia
De Martino, Viviana
D’Agostini, Matteo
Porzio, Ottavia
Cipriani, Cristiana
Minisola, Salvatore
De Vito, Rita
Vecchio, Davide
Gonfiantini, Michaela Veronika
Jenkner, Alessandro
Bartuli, Andrea
Del Fattore, Andrea
author_sort Rossi, Michela
collection PubMed
description Gorham-Stout disease (GSD) is a very rare syndrome displaying excessive bone erosion and vascular lesion. Due to the rarity of the disease and to the limited studies, its etiopathogenesis is not entirely known. The involvement of immune system in the progressive osteolysis was recently suggested. Indeed, extensive reciprocal interactions between the immune and skeletal systems have been demonstrated. This study aimed to evaluate alterations of immune cells in GSD. An increase of CD8+ cells and reduction of CD4+ and CD4+CD25+CD127(low) cells was revealed in patients. Interestingly, patients’ regulatory T cells maintain the ability to respond to extracellular stimuli and to regulate osteoclastogenesis; GSD cells proliferate under aCD3/CD28 signal reaching similar levels to those observed in control culture and exert their immunomodulatory activity on effector T cells. GSD Treg cells preserved their inhibitory effects on the osteoclastogenesis. These results suggest that stimulation of Treg cells could open the way for the identification and testing of new therapeutic approaches for patients affected by GSD.
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spelling pubmed-84300392021-09-11 Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease Rossi, Michela Rana, Ippolita Buonuomo, Paola Sabrina Battafarano, Giulia De Martino, Viviana D’Agostini, Matteo Porzio, Ottavia Cipriani, Cristiana Minisola, Salvatore De Vito, Rita Vecchio, Davide Gonfiantini, Michaela Veronika Jenkner, Alessandro Bartuli, Andrea Del Fattore, Andrea Front Cell Dev Biol Cell and Developmental Biology Gorham-Stout disease (GSD) is a very rare syndrome displaying excessive bone erosion and vascular lesion. Due to the rarity of the disease and to the limited studies, its etiopathogenesis is not entirely known. The involvement of immune system in the progressive osteolysis was recently suggested. Indeed, extensive reciprocal interactions between the immune and skeletal systems have been demonstrated. This study aimed to evaluate alterations of immune cells in GSD. An increase of CD8+ cells and reduction of CD4+ and CD4+CD25+CD127(low) cells was revealed in patients. Interestingly, patients’ regulatory T cells maintain the ability to respond to extracellular stimuli and to regulate osteoclastogenesis; GSD cells proliferate under aCD3/CD28 signal reaching similar levels to those observed in control culture and exert their immunomodulatory activity on effector T cells. GSD Treg cells preserved their inhibitory effects on the osteoclastogenesis. These results suggest that stimulation of Treg cells could open the way for the identification and testing of new therapeutic approaches for patients affected by GSD. Frontiers Media S.A. 2021-08-27 /pmc/articles/PMC8430039/ /pubmed/34513837 http://dx.doi.org/10.3389/fcell.2021.706596 Text en Copyright © 2021 Rossi, Rana, Buonuomo, Battafarano, De Martino, D’Agostini, Porzio, Cipriani, Minisola, De Vito, Vecchio, Gonfiantini, Jenkner, Bartuli and Del Fattore. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Rossi, Michela
Rana, Ippolita
Buonuomo, Paola Sabrina
Battafarano, Giulia
De Martino, Viviana
D’Agostini, Matteo
Porzio, Ottavia
Cipriani, Cristiana
Minisola, Salvatore
De Vito, Rita
Vecchio, Davide
Gonfiantini, Michaela Veronika
Jenkner, Alessandro
Bartuli, Andrea
Del Fattore, Andrea
Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title_full Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title_fullStr Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title_full_unstemmed Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title_short Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease
title_sort stimulation of treg cells to inhibit osteoclastogenesis in gorham-stout disease
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430039/
https://www.ncbi.nlm.nih.gov/pubmed/34513837
http://dx.doi.org/10.3389/fcell.2021.706596
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