Quantification and molecular characterization of regulatory T cells in connective tissue diseases

结缔组织 免疫学 结缔组织病 流式细胞术 自身抗体 FOXP3型 表型 皮肌炎 混合性结缔组织病 自身免疫性疾病 自身免疫 系统性红斑狼疮 生物 疾病 医学 病理 抗体 免疫系统 基因 生物化学
作者
Leontina Bănică,Leontina Bănică,Alina Besliu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Cristina Chiţonu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Cristina Chiţonu,Simona Paraschiv,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Cristina Chiţonu,Simona Paraschiv,Monica Balteanu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Cristina Chiţonu,Simona Paraschiv,Monica Balteanu,M Stefănescu,Leontina Bănică,Alina Besliu,Gina Cecilia Pistol,Crina Stăvaru,Ruxandra Ionescu,Ana‐Maria Forsea,Cristina Tănăseanu,Sergiu Dumitrache,Dan Oțelea,Isabela Tamşulea,S Tănăseanu,Cristina Chiţonu,Simona Paraschiv,Monica Balteanu,M Stefănescu,Cristiana Matache
出处
期刊:Autoimmunity [Informa]
卷期号:42 (1): 41-49 被引量:87
标识
DOI:10.1080/08916930802282651
摘要

The aim of our study was to investigate and characterize regulatory T cells (Treg) in peripheral blood of patients with connective tissue diseases (Systemic lupus erythematosus, systemic sclerosis, Sjögren's syndrome, poly- and dermatomyositis) as compared with blood from healthy controls. Treg cells were quantified and phenotypically characterized by flow cytometry while the expression level of Foxp3 mRNA was evaluated by real time PCR. A reduced percentage of peripheral blood Treg cells was found in patients than in controls, irrespective of the type of connective tissue disease. Treg cells, especially those expressing one of the phenotypical markers, seemed to differ not only between patients and healthy controls but also among types of diseases. Additionally, the presence of autoantibodies as well as disease activity appeared to be correlated with particular Treg cell populations, especially those expressing one of the examined phenotypical markers. Correlations with therapy suggested that glucocorticoids plus antimalarial or other immunosuppressor drugs diminished the percentage of Treg cells, especially of those with memory phenotype. These findings indicated dysregulations at the level of Treg cells and suggested an involvement of these cells in the pathology of connective tissue diseases. Moreover, our data are in agreement with the suggestion that Treg cells could be therapeutic targets for some autoimmune diseases.
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