Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease
This study aimed to search the correlation among immunological profiles and clinical phenotypes of scleroderma in well-characterized groups of scleroderma patients, comparing forty-nine scleroderma patients stratified according to specific clinical phenotypes with forty-nine healthy controls. Five i...
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doaj-ba848118b7834135913c910dab08e0182020-11-24T21:44:37ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/148293148293Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma DiseaseJosé Manuel López-Cacho0Soledad Gallardo1Manuel Posada2Miriam Aguerri3David Calzada4Teodoro Mayayo5María Luisa González-Rodríguez6Antonio María Rabasco7Carlos Lahoz8Blanca Cárdaba9Department of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainInstitute of Rare Diseases Research, Carlos III Institute of Health, EuroBioBank, and CIBERER, 28029 Madrid, SpainDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainSani-Red S.L, Barcelona Scientific Park, 08013 Barcelona, SpainDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Seville, 41012 Seville, SpainDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Seville, 41012 Seville, SpainDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, SpainThis study aimed to search the correlation among immunological profiles and clinical phenotypes of scleroderma in well-characterized groups of scleroderma patients, comparing forty-nine scleroderma patients stratified according to specific clinical phenotypes with forty-nine healthy controls. Five immunological cell subpopulations (B, CD4+ and CD8+ T-cells, NK, and monocytes) and their respective stages of apoptosis and activation were analyzed by flow cytometry, in samples of peripheral blood mononuclear cells (PBMCs). Analyses of results were stratified according to disease stage, time since the diagnosis, and visceral damage (pulmonary fibrosis, pulmonary hypertension, and cardiac affliction) and by time of treatment with corticosteroids. An increase in the percentages of monocytes and a decrease in the B cells were mainly related to the disease progression. A general apoptosis decrease was found in all phenotypes studied, except in localized scleroderma. An increase of B and NK cells activation was found in patients diagnosed more than 10 years ago. Specific cell populations like monocytes, NK, and B cells were associated with the type of affected organ. This study shows how, in a heterogeneous disease, proper patient’s stratification according to clinical phenotypes allows finding specific cellular profiles. Our data may lead to improvements in the knowledge of prognosis factors and to aid in the analysis of future specific therapies.http://dx.doi.org/10.1155/2014/148293 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
José Manuel López-Cacho Soledad Gallardo Manuel Posada Miriam Aguerri David Calzada Teodoro Mayayo María Luisa González-Rodríguez Antonio María Rabasco Carlos Lahoz Blanca Cárdaba |
spellingShingle |
José Manuel López-Cacho Soledad Gallardo Manuel Posada Miriam Aguerri David Calzada Teodoro Mayayo María Luisa González-Rodríguez Antonio María Rabasco Carlos Lahoz Blanca Cárdaba Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease BioMed Research International |
author_facet |
José Manuel López-Cacho Soledad Gallardo Manuel Posada Miriam Aguerri David Calzada Teodoro Mayayo María Luisa González-Rodríguez Antonio María Rabasco Carlos Lahoz Blanca Cárdaba |
author_sort |
José Manuel López-Cacho |
title |
Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease |
title_short |
Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease |
title_full |
Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease |
title_fullStr |
Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease |
title_full_unstemmed |
Association of Immunological Cell Profiles with Specific Clinical Phenotypes of Scleroderma Disease |
title_sort |
association of immunological cell profiles with specific clinical phenotypes of scleroderma disease |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2014-01-01 |
description |
This study aimed to search the correlation among immunological profiles and clinical phenotypes of scleroderma in well-characterized groups of scleroderma patients, comparing forty-nine scleroderma patients stratified according to specific clinical phenotypes with forty-nine healthy controls. Five immunological cell subpopulations (B, CD4+ and CD8+ T-cells, NK, and monocytes) and their respective stages of apoptosis and activation were analyzed by flow cytometry, in samples of peripheral blood mononuclear cells (PBMCs). Analyses of results were stratified according to disease stage, time since the diagnosis, and visceral damage (pulmonary fibrosis, pulmonary hypertension, and cardiac affliction) and by time of treatment with corticosteroids. An increase in the percentages of monocytes and a decrease in the B cells were mainly related to the disease progression. A general apoptosis decrease was found in all phenotypes studied, except in localized scleroderma. An increase of B and NK cells activation was found in patients diagnosed more than 10 years ago. Specific cell populations like monocytes, NK, and B cells were associated with the type of affected organ. This study shows how, in a heterogeneous disease, proper patient’s stratification according to clinical phenotypes allows finding specific cellular profiles. Our data may lead to improvements in the knowledge of prognosis factors and to aid in the analysis of future specific therapies. |
url |
http://dx.doi.org/10.1155/2014/148293 |
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