Disturbed Th1, Th2, Th17 and T-reg balance in patients with systemic lupus erythematosus

  • Sebastian Dolff*
  • , Marc Bijl
  • , Minke G. Huitema
  • , Pieter C. Limburg
  • , Cees G. M. Kallenberg
  • , Wayel H. Abdulahad
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

136 Citations (Scopus)

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 languageEnglish
Pages (from-to)197-204
Number of pages8
JournalClinical Immunology
Volume141
Issue number2
DOIs
Publication statusPublished - Nov-2011

Keywords

  • SLE
  • T-helper cells
  • Regulatory T-cells
  • IL-17
  • WEGENERS-GRANULOMATOSIS
  • PERIPHERAL-BLOOD
  • CELLS
  • EXPRESSION
  • LYMPHOCYTES
  • REMISSION
  • NEPHRITIS
  • KIDNEYS
  • IL-17

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