Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease

In order to identify disease biomarkers for the clinical and therapeutic management of autoimmune diseases such as systemic sclerosis (SSc) and undifferentiated connective tissue disease (UCTD), we have explored the setting of peripheral T regulatory (T reg) cells and assessed an expanded profile of...

Full description

Saved in:
Bibliographic Details
Main Authors: Paola Cordiali-Fei, Anna Mussi, Giovanna D'Agosto, Elisabetta Trento, Valentina Bordignon, Silvana Trincone, Antonella Vento, Isabella Sperduti, Antonio Cristaudo, Fabrizio Ensoli
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2013/390563
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832552851756285952
author Paola Cordiali-Fei
Anna Mussi
Giovanna D'Agosto
Elisabetta Trento
Valentina Bordignon
Silvana Trincone
Antonella Vento
Isabella Sperduti
Antonio Cristaudo
Fabrizio Ensoli
author_facet Paola Cordiali-Fei
Anna Mussi
Giovanna D'Agosto
Elisabetta Trento
Valentina Bordignon
Silvana Trincone
Antonella Vento
Isabella Sperduti
Antonio Cristaudo
Fabrizio Ensoli
author_sort Paola Cordiali-Fei
collection DOAJ
description In order to identify disease biomarkers for the clinical and therapeutic management of autoimmune diseases such as systemic sclerosis (SSc) and undifferentiated connective tissue disease (UCTD), we have explored the setting of peripheral T regulatory (T reg) cells and assessed an expanded profile of autoantibodies in patients with SSc, including either limited (lcSSc) or diffuse (dcSSc) disease, and in patients presenting with clinical signs and symptoms of UCTD. A large panel of serum antibodies directed towards nuclear, nucleolar, and cytoplasmic antigens, including well-recognized molecules as well as less frequently tested antigens, was assessed in order to determine whether different antibody profiles might be associated with distinct clinical settings. Beside the well-recognized association between lcSSc and anti-centromeric or dcSSC and anti-topoisomerase-I antibodies, we found a significative association between dcSSc and anti-SRP or anti-PL-7/12 antibodies. In addition, two distinct groups emerged on the basis of anti-RNP or anti-PM-Scl 75/100 antibody production among UCTD patients. The levels of T reg cells were significantly lower in patients with SSc as compared to patients with UCTD or to healthy controls; in patients with lcSSc, T reg cells were inversely correlated to disease duration, suggesting that their levels may represent a marker of disease progression.
format Article
id doaj-art-5d38e2f9428744f8a017e1419ea06ba1
institution Kabale University
issn 1740-2522
1740-2530
language English
publishDate 2013-01-01
publisher Wiley
record_format Article
series Clinical and Developmental Immunology
spelling doaj-art-5d38e2f9428744f8a017e1419ea06ba12025-02-03T05:57:41ZengWileyClinical and Developmental Immunology1740-25221740-25302013-01-01201310.1155/2013/390563390563Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue DiseasePaola Cordiali-Fei0Anna Mussi1Giovanna D'Agosto2Elisabetta Trento3Valentina Bordignon4Silvana Trincone5Antonella Vento6Isabella Sperduti7Antonio Cristaudo8Fabrizio Ensoli9Clinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Dermatology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Dermatology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyBiostatistic Unit, Regina Elena Cancer Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Dermatology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyClinical Pathology and Microbiology, San Gallicano Dermatology Institute, Via Elio Chianesi 53, 00144 Rome, ItalyIn order to identify disease biomarkers for the clinical and therapeutic management of autoimmune diseases such as systemic sclerosis (SSc) and undifferentiated connective tissue disease (UCTD), we have explored the setting of peripheral T regulatory (T reg) cells and assessed an expanded profile of autoantibodies in patients with SSc, including either limited (lcSSc) or diffuse (dcSSc) disease, and in patients presenting with clinical signs and symptoms of UCTD. A large panel of serum antibodies directed towards nuclear, nucleolar, and cytoplasmic antigens, including well-recognized molecules as well as less frequently tested antigens, was assessed in order to determine whether different antibody profiles might be associated with distinct clinical settings. Beside the well-recognized association between lcSSc and anti-centromeric or dcSSC and anti-topoisomerase-I antibodies, we found a significative association between dcSSc and anti-SRP or anti-PL-7/12 antibodies. In addition, two distinct groups emerged on the basis of anti-RNP or anti-PM-Scl 75/100 antibody production among UCTD patients. The levels of T reg cells were significantly lower in patients with SSc as compared to patients with UCTD or to healthy controls; in patients with lcSSc, T reg cells were inversely correlated to disease duration, suggesting that their levels may represent a marker of disease progression.http://dx.doi.org/10.1155/2013/390563
spellingShingle Paola Cordiali-Fei
Anna Mussi
Giovanna D'Agosto
Elisabetta Trento
Valentina Bordignon
Silvana Trincone
Antonella Vento
Isabella Sperduti
Antonio Cristaudo
Fabrizio Ensoli
Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
Clinical and Developmental Immunology
title Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
title_full Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
title_fullStr Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
title_full_unstemmed Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
title_short Assessment of T Regulatory Cells and Expanded Profiling of Autoantibodies May Offer Novel Biomarkers for the Clinical Management of Systemic Sclerosis and Undifferentiated Connective Tissue Disease
title_sort assessment of t regulatory cells and expanded profiling of autoantibodies may offer novel biomarkers for the clinical management of systemic sclerosis and undifferentiated connective tissue disease
url http://dx.doi.org/10.1155/2013/390563
work_keys_str_mv AT paolacordialifei assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT annamussi assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT giovannadagosto assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT elisabettatrento assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT valentinabordignon assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT silvanatrincone assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT antonellavento assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT isabellasperduti assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT antoniocristaudo assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease
AT fabrizioensoli assessmentoftregulatorycellsandexpandedprofilingofautoantibodiesmayoffernovelbiomarkersfortheclinicalmanagementofsystemicsclerosisandundifferentiatedconnectivetissuedisease