Article (Scientific journals)
Anti-inflammatory and antiproliferative actions of PPAR-gamma agonists on T lymphocytes derived from MS patients.
Schmidt, Stephan; Moric, Edin; Schmidt, Martina et al.
2004In Journal of Leukocyte Biology, 75 (3), p. 478 - 485
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Keywords :
Adjuvants, Immunologic; Anti-Inflammatory Agents; Cytokines; Receptors, Cytoplasmic and Nuclear; Thiazolidinediones; Transcription Factors; ciglitazone; Pioglitazone; Adjuvants, Immunologic/pharmacology; Adolescent; Adult; Anti-Inflammatory Agents/pharmacology; Case-Control Studies; Cell Division/drug effects; Cell Division/immunology; Cytokines/metabolism; Female; Humans; Lymphocyte Activation/drug effects; Lymphocyte Activation/immunology; Male; Middle Aged; Multiple Sclerosis/immunology; Receptors, Cytoplasmic and Nuclear/agonists; T-Lymphocytes/cytology; T-Lymphocytes/drug effects; T-Lymphocytes/immunology; Thiazolidinediones/pharmacology; Transcription Factors/agonists; EAE; IFN-γ; TNF-α; Immunology and Allergy; Immunology; Cell Biology; IFN-gamma; TNF-alpha
Abstract :
[en] Peroxisomal proliferator-activated receptors (PPARs) belong to a nuclear receptor superfamily of ligand-activated transcription factors. The PPAR-gamma isoform is expressed in human T lymphocytes, and oral administration of PPAR-gamma agonists ameliorates the clinical course and histopathological features in experimental autoimmune encephalomyelitis, an animal model for multiple sclerosis, suggesting a potential role for PPAR-gamma agonists in the treatment of autoimmune diseases. To assess a potential therapeutic role of PPAR-gamma agonists in multiple sclerosis, we compared the immunomodulatory effects of the thiazolidinedione (TZD) drugs pioglitazone (PIO) and ciglitazone and the non-TZD PPAR-gamma agonist GW347845 on human T leukemia cells (Jurkat cells) and phytohemagglutinin (PHA)-stimulated peripheral blood mononuclear cells (PBMCs) derived from 21 multiple sclerosis patients and 12 healthy donors. PIO, ciglitazone, and GW347845 suppressed PHA-induced T cell proliferation by 40-50% and secretion of interferon-gamma and tumor necrosis factor alpha, by 30-50%. Inhibition of proliferation was increased to approximately 80% and that of proinflammatory cytokine secretion, to 80-90% when PBMCs were first preincubated with PPAR-gamma agonists and re-exposed at the time of PHA stimulation, indicating a sensitizing effect of PPAR-gamma agonists. Inhibition of proliferation was also observed in the tetanus toxoid-specific T cell line KHS.TT2, albeit to a lesser extent. The antiproliferative effects of PIO and GW347845 were accompanied by a decrease of cell viability. Electron microscopy and Western blot analysis revealed DNA condensation and down-regulation of bcl-2, suggesting the induction of apoptosis in activated T lymphocytes. In summary, the data support the potential use of PPAR-gamma agonists as immunomodulatory, therapeutic agents for autoimmune diseases.
Disciplines :
Neurology
Author, co-author :
Schmidt, Stephan;  Department of Neurology, University of Bonn, Germany
Moric, Edin;  Department of Neurology, University of Bonn, Bonn, Germany
Schmidt, Martina;  Department of Neurology, University of Bonn, Bonn, Germany
Sastre, Magdalena;  Department of Neurology, University of Bonn, Bonn, Germany
Feinstein, Douglas L;  Department of Anesthesiology, University of Illinois, Chicago, IL, United States
HENEKA, Michael  ;  Department of Neurology, University of Bonn, Bonn, Germany ; Neurologische Univ. Klin. Bonn, 53105 Bonn, Germany
External co-authors :
yes
Language :
English
Title :
Anti-inflammatory and antiproliferative actions of PPAR-gamma agonists on T lymphocytes derived from MS patients.
Publication date :
March 2004
Journal title :
Journal of Leukocyte Biology
ISSN :
0741-5400
Publisher :
Oxford University Press (OUP), England
Volume :
75
Issue :
3
Pages :
478 - 485
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
Gemeinnützige Hertie-Stiftung
Takeda Pharmaceuticals
GlaxoSmithKline
National Multiple Sclerosis Society
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