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Cytotherapy ; 13(7): 835-47, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21506890

ABSTRACT

BACKGROUND AIMS: Behcet's disease (BD) is a chronic, multisystemic inflammatory disorder with arthritic, gastrointestinal, mucocutaneous, ocular, vascular and central nervous system involvement. It is well known that CD4(+) CD25(+) T-regulatory (Treg) cells prevent harmful immune responses to self- and non-self-antigens. In the present study, the role of Treg cells in herpes simplex virus (HSV)-induced BD-like symptoms was investigated. METHODS: HSV type 1 (F strain) inoculation of the earlobe of ICR mice has been shown to induce the development of BD-like symptoms. To determine whether the effect of Treg was associated with change in BD-like symptoms, CD4(+) CD25(+) T cells from the splenocytes of normal mice were adoptively transferred intravenously. Treg cells of splenocytes were significantly elevated following the transfer of 3 × 10(5) CD4(+) CD25(+) T cells to BD-like mice compared with the control group. RESULTS: The transfer of CD4(+) CD25(+) T cells to BD mice improved the symptoms, and the serum protein levels of interleukin (IL)-10, IL-6 and IL-17 were significantly altered compared with the control groups. Intravenous injection of anti-CD25 antibody to BD mice reduced the frequency of CD4(+) CD25(+) T cells and increased the BD severity score. We confirmed the influence of CD4(+) CD25(+) T cells on BD-like mice. CONCLUSIONS: These results show that up-regulation of the CD4(+) CD25(+) T cells in BD-like mice improves the inflammatory symptoms, while down-regulation of CD25(+) T cells is associated with deteriorated symptoms. Furthermore, these findings are correlated with changes in pro-inflammatory and anti-inflammatory cytokine levels.


Subject(s)
Behcet Syndrome/immunology , Behcet Syndrome/therapy , CD4-Positive T-Lymphocytes/immunology , Interleukin-2 Receptor alpha Subunit/immunology , T-Lymphocytes, Regulatory/immunology , Adoptive Transfer , Animals , Behcet Syndrome/metabolism , Behcet Syndrome/virology , Cells, Cultured , Disease Models, Animal , Forkhead Transcription Factors/immunology , Forkhead Transcription Factors/metabolism , Herpesvirus 1, Human/pathogenicity , Interferon-gamma/blood , Interleukin-10/blood , Interleukin-17/blood , Interleukin-6/blood , Male , Mice , Mice, Inbred ICR , Spleen/cytology , Spleen/immunology , Transforming Growth Factor beta/blood , Tumor Necrosis Factor-alpha/blood , Up-Regulation
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