Disturbed Th1, Th2, Th17 and Treg balance in patients with systemic lupus erythematosus

被引:121
作者
Dolff, Sebastian [1 ,2 ]
Bijl, Marc [1 ]
Huitema, Minke G. [1 ]
Limburg, Pieter C. [1 ]
Kallenberg, Cees G. M. [1 ]
Abdulahad, Wayel H. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol & Clin Immunol, NL-9700 RB Groningen, Netherlands
[2] Univ Duisburg Essen, Univ Hosp Essen, Dept Nephrol, Duisburg, Germany
关键词
SLE; T-helper cells; Regulatory T-cells; IL-17; WEGENERS-GRANULOMATOSIS; PERIPHERAL-BLOOD; CELLS; EXPRESSION; LYMPHOCYTES; REMISSION; NEPHRITIS; KIDNEYS; IL-17;
D O I
10.1016/j.clim.2011.08.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:197 / 204
页数:8
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