Abstract
Systemic lupus erythematosus (SLE) is an autoimmune disease accompanied by disturbed T-cell homeostasis. Dysbalance of T-helper-cell (Th) subsets (Th1/Th2/Th17) and regulatory T-cells (T-regs) is suggested to contribute to the pathogenesis of SLE. Recent reports suggest functional deviation of T-regs in terms of producing IL-17A, a process that may be aberrant in SLE. Therefore, we analyzed these T-cell subsets in SLE to test the hypothesis that aberrant T-cell subset skewing is present in SLE-patients. We investigated simultaneously the intracellular cytokines IFN-gamma, IL-4 and IL-17A in CD4(+)T-cells as well as in T-regs. Skewing of T-cell subsets towards Th17 cells was observed in SLE-patients. Although the proportion of T-regs was similar between SLE-patients and healthy controls, the ability of T-regs to express IFN-gamma and IL17A was impaired in SLE-patients. Even in quiescent SLE-patients T-cell homeostasis is aberrant in terms of skewing towards IL-17 producing T-cells. (C) 2011 Elsevier Inc. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 197-204 |
| Number of pages | 8 |
| Journal | Clinical Immunology |
| Volume | 141 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Nov-2011 |
Keywords
- SLE
- T-helper cells
- Regulatory T-cells
- IL-17
- WEGENERS-GRANULOMATOSIS
- PERIPHERAL-BLOOD
- CELLS
- EXPRESSION
- LYMPHOCYTES
- REMISSION
- NEPHRITIS
- KIDNEYS
- IL-17