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1.
Clin Exp Immunol ; 189(1): 113-119, 2017 07.
Article in English | MEDLINE | ID: mdl-28253537

ABSTRACT

Phosphotyrosine phosphatases (PTPs) control phosphorylation levels and, consequently, regulate the output of intracellular signalling networks in health and disease. Despite the high number of PTPs expressed in CD4 T cells and their involvement in autoimmunity, information about the expression profile of PTPs in these cells has not been obtained in patients diagnosed with autoimmune diseases. Here, we compare the expression profile of PTPs in CD4 T cells of healthy volunteers and patients submitted to an early arthritis clinic, due to suspicion of rheumatoid arthritis, an autoimmune disease mediated by CD4 T cells. We found lower transcript levels of the mitogen-activated protein kinase (MAPK) phosphatase dual-specific phosphatase-7 (DUSP7) and the cell division cycle-25B (CDC25B) in T cells of patients. While the low expression level of DUSP7 was restricted to patients with positive rheumatoid factor and anti-citrullinated protein antibodies, the altered expression of CDC25B correlated with the activity of the disease. Low levels of CDC25B might contribute to the progression of the autoimmune arthritis and/or might be consequence of the inflammatory environment in the active disease. The possible role of DUSP7 and CDC25B as biomarkers of the disease in clinical protocols is discussed.


Subject(s)
Arthritis/metabolism , CD4-Positive T-Lymphocytes/metabolism , Dual-Specificity Phosphatases/metabolism , cdc25 Phosphatases/metabolism , Adult , Aged , Autoimmune Diseases/metabolism , Biomarkers/metabolism , Dual-Specificity Phosphatases/genetics , Female , Humans , Male , Middle Aged , Phosphorylation , Prospective Studies , RNA, Messenger/metabolism , Spain , cdc25 Phosphatases/genetics
2.
Clin Exp Immunol ; 170(3): 365-74, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23121677

ABSTRACT

Accumulating evidence shows that galectins play roles in the initiation and resolution phases of inflammatory responses by promoting anti- or proinflammatory effects. This study investigated the presence of three members of the galectin family (galectin-1, -3 and -9) in induced sputum samples of asthma patients, as well as their possible implication in the immunopathogenesis of human asthma. Levels of interleukin (IL)-5, IL-13, and galectins were determined in leucocytes isolated from induced sputum samples by reverse transcription-polymerase chain reaction (RT-PCR) immunofluorescence and flow cytometry. High levels of IL-5 and IL-13 mRNA were detected in sputum cells from asthma patients. In parallel, immunoregulatory proteins galectin-1 and galectin-9 showed a reduced expression on macrophages from sputum samples compared with cells from healthy donors. In-vitro immunoassays showed that galectin-1 and galectin-9, but not galectin-3, are able to induce the production of IL-10 by peripheral blood mononuclear cells from healthy donors. These findings indicate that macrophages from sputum samples of asthma patients express low levels of galectin-1 and galectin-9, favouring the exacerbated immune response observed in this disease.


Subject(s)
Asthma/genetics , Asthma/metabolism , Galectin 1/genetics , Gene Expression Regulation , Leukocytes/metabolism , Adult , Aged , Case-Control Studies , Cytokines/genetics , Cytokines/metabolism , Female , Galectin 1/metabolism , Galectin 3/genetics , Galectin 3/metabolism , Humans , Macrophages/immunology , Macrophages/metabolism , Male , Middle Aged , Respiratory Function Tests , Sputum/immunology , Th2 Cells/immunology , Th2 Cells/metabolism , Young Adult
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