T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives

Historically, primary Sjögren’s syndrome (pSS) was thought to be a T helper (h) 1 driven disease due to the predominance of CD4+T lymphocytes and their products in target organs and peripheral blood of patients. In the last decades, the identification of a number of T cell subsets, including Th17, T...

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Main Authors: Alessia Alunno, Francesco Carubbi, Onelia Bistoni, Sara Caterbi, Elena Bartoloni, Giulia Mirabelli, Francesca Cannarile, Paola Cipriani, Roberto Giacomelli, Roberto Gerli
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/243723
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author Alessia Alunno
Francesco Carubbi
Onelia Bistoni
Sara Caterbi
Elena Bartoloni
Giulia Mirabelli
Francesca Cannarile
Paola Cipriani
Roberto Giacomelli
Roberto Gerli
author_facet Alessia Alunno
Francesco Carubbi
Onelia Bistoni
Sara Caterbi
Elena Bartoloni
Giulia Mirabelli
Francesca Cannarile
Paola Cipriani
Roberto Giacomelli
Roberto Gerli
author_sort Alessia Alunno
collection DOAJ
description Historically, primary Sjögren’s syndrome (pSS) was thought to be a T helper (h) 1 driven disease due to the predominance of CD4+T lymphocytes and their products in target organs and peripheral blood of patients. In the last decades, the identification of a number of T cell subsets, including Th17, T regulatory (Treg), and follicular helper T cells, challenged this long-standing paradigm and prompted to identify their role in pSS pathogenesis. In addition the impact of abnormal proinflammatory cytokine production, such as IL-6, IL-17, IL-22, and IL-23, has also attracted considerable attention. However, although several studies have been carried out in experimental models and patients with pSS, many aspects concerning the role of Treg cells and IL-17/Th17 cell system in pSS pathogenesis are not fully elucidated. In particular, the role played by different IL-17-producing T cell subsets as well as the effects of pharmacological therapies on Treg/Th17 cell balance represents an intriguing issue. The aim of this review article is to provide an overview of current knowledge on Treg cells and IL-17-producing T cells in pSS pathogenesis. We believe that these insights into pSS pathogenesis may provide the basis for successful therapeutic intervention in this disease.
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institution Kabale University
issn 0962-9351
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language English
publishDate 2015-01-01
publisher Wiley
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series Mediators of Inflammation
spelling doaj-art-7f7830476cd44176bc83e715107336722025-02-03T05:52:00ZengWileyMediators of Inflammation0962-93511466-18612015-01-01201510.1155/2015/243723243723T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and PerspectivesAlessia Alunno0Francesco Carubbi1Onelia Bistoni2Sara Caterbi3Elena Bartoloni4Giulia Mirabelli5Francesca Cannarile6Paola Cipriani7Roberto Giacomelli8Roberto Gerli9Rheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, 67100 L’Aquila, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyRheumatology Unit, Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, 67100 L’Aquila, ItalyRheumatology Unit, Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, 67100 L’Aquila, ItalyRheumatology Unit, Department of Medicine, University of Perugia, 06123 Perugia, ItalyHistorically, primary Sjögren’s syndrome (pSS) was thought to be a T helper (h) 1 driven disease due to the predominance of CD4+T lymphocytes and their products in target organs and peripheral blood of patients. In the last decades, the identification of a number of T cell subsets, including Th17, T regulatory (Treg), and follicular helper T cells, challenged this long-standing paradigm and prompted to identify their role in pSS pathogenesis. In addition the impact of abnormal proinflammatory cytokine production, such as IL-6, IL-17, IL-22, and IL-23, has also attracted considerable attention. However, although several studies have been carried out in experimental models and patients with pSS, many aspects concerning the role of Treg cells and IL-17/Th17 cell system in pSS pathogenesis are not fully elucidated. In particular, the role played by different IL-17-producing T cell subsets as well as the effects of pharmacological therapies on Treg/Th17 cell balance represents an intriguing issue. The aim of this review article is to provide an overview of current knowledge on Treg cells and IL-17-producing T cells in pSS pathogenesis. We believe that these insights into pSS pathogenesis may provide the basis for successful therapeutic intervention in this disease.http://dx.doi.org/10.1155/2015/243723
spellingShingle Alessia Alunno
Francesco Carubbi
Onelia Bistoni
Sara Caterbi
Elena Bartoloni
Giulia Mirabelli
Francesca Cannarile
Paola Cipriani
Roberto Giacomelli
Roberto Gerli
T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
Mediators of Inflammation
title T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
title_full T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
title_fullStr T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
title_full_unstemmed T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
title_short T Regulatory and T Helper 17 Cells in Primary Sjögren’s Syndrome: Facts and Perspectives
title_sort t regulatory and t helper 17 cells in primary sjogren s syndrome facts and perspectives
url http://dx.doi.org/10.1155/2015/243723
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