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

Copyright © 2011 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 141(2011), 2 vom: 15. Nov., Seite 197-204
1. Verfasser: Dolff, Sebastian (VerfasserIn)
Weitere Verfasser: Bijl, Marc, Huitema, Minke G, Limburg, Pieter C, Kallenberg, Cees G M, Abdulahad, Wayel H
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't FOXP3 protein, human Forkhead Transcription Factors IL17A protein, human Interleukin-17 Interleukin-4 207137-56-2 Interferon-gamma 82115-62-6
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245 1 0 |a Disturbed Th1, Th2, Th17 and T(reg) balance in patients with systemic lupus erythematosus 
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520 |a Copyright © 2011 Elsevier Inc. All rights reserved. 
520 |a 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-γ, 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-γ 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 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a FOXP3 protein, human  |2 NLM 
650 7 |a Forkhead Transcription Factors  |2 NLM 
650 7 |a IL17A protein, human  |2 NLM 
650 7 |a Interleukin-17  |2 NLM 
650 7 |a Interleukin-4  |2 NLM 
650 7 |a 207137-56-2  |2 NLM 
650 7 |a Interferon-gamma  |2 NLM 
650 7 |a 82115-62-6  |2 NLM 
700 1 |a Bijl, Marc  |e verfasserin  |4 aut 
700 1 |a Huitema, Minke G  |e verfasserin  |4 aut 
700 1 |a Limburg, Pieter C  |e verfasserin  |4 aut 
700 1 |a Kallenberg, Cees G M  |e verfasserin  |4 aut 
700 1 |a Abdulahad, Wayel H  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Clinical immunology (Orlando, Fla.)  |d 1999  |g 141(2011), 2 vom: 15. Nov., Seite 197-204  |w (DE-627)NLM098196855  |x 1521-7035  |7 nnns 
773 1 8 |g volume:141  |g year:2011  |g number:2  |g day:15  |g month:11  |g pages:197-204 
856 4 0 |u http://dx.doi.org/10.1016/j.clim.2011.08.005  |3 Volltext 
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