Statin-induced immunomodulatory effects on human T cells in vivo
Thomas Fehr, Christian R. Kahlert, Walter Fierz, Helen I Joller-Jemelka, Walter F Riesen, Hans Rickli, Rudolf P Wüthrich & Peter Ammann
abstract
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Statins are widely used for treatment of hypercholesterolemia.
Recent experimental studies revealed that these drugs also exert
anti-inflammatory effects. The aim of this study was to assess
immunomodulatory effects of statins in humans in vivo. Twenty-seven
healthy volunteers were analyzed for serum cytokines and acute phase
proteins, HLA-DR and CD38 expression on T cells and
superantigen-mediated T cell activation ex vivo before and after 14
days of statin treatment. First, simvastatin 40 mg was compared to
atorvastatin 20 mg. Second, two different doses of simvastatin (20
and 40 mg) were tested. Atorvastatin treatment led to a significant
down-regulation of HLA-DR and the CD38 activation marker on
peripheral T cells, whereas simvastatin up-regulated both of these
molecules. In contrast, superantigen-mediated T cell activation was
inhibited by simvastatin and enhanced by atorvastatin. No
significant effect of statin treatment on inflammatory serum markers
was detected. Thus, immunomodulatory effects of statins on human T
cells are first demonstrated in vivo and are differentially induced
by two different statins: atorvastatin led to a major
histocompatibility class II (MHC II) antigens down-regulation and
may therefore be investigated for treatment of chronic transplant
rejection; simvastatin inhibited superantigen-mediated T cell
activation, which might explain reduced mortality of
simvastatin-treated patients with staphylococcal bacteremia.
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citation
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Fehr T, Kahlert C R, Fierz W, Joller-Jemelka H I, Riesen W F, Rickli
H, Wüthrich R P, Ammann P. Statin-induced immunomodulatory effects
on human T cells in vivo. Atherosclerosis 2004; 175:83-90.
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type
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journal paper/review (English)
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date of publishing
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7-2004
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journal title
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Atherosclerosis (175/1)
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ISSN print
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0021-9150
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pages
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83-90
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PubMed
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15186950
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DOI
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10.1016/j.atherosclerosis.2004.02.016
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