Source:http://linkedlifedata.com/resource/pubmed/id/16947529
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2006-10-2
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pubmed:abstractText |
Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown origin. Current treatment options are often ineffective or poorly tolerated. Recent observations have revealed mitochondrial hyperpolarization and enhanced Ca2+ fluxing in T cells from SLE patients. Rapamycin, a lipophilic macrolide antibiotic that regulates mitochondrial transmembrane potential and Ca2+ fluxing, has been used safely and effectively to treat renal transplant rejection since 1999. In addition, rapamycin has been shown to ameliorate T cell function and to prolong survival in lupus-prone MRL/lpr mice. We therefore undertook the present study to investigate whether rapamycin is beneficial in patients with SLE.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0004-3591
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2983-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16947529-Adolescent,
pubmed-meshheading:16947529-Adult,
pubmed-meshheading:16947529-Anti-Bacterial Agents,
pubmed-meshheading:16947529-Calcium Signaling,
pubmed-meshheading:16947529-Cell Culture Techniques,
pubmed-meshheading:16947529-Flow Cytometry,
pubmed-meshheading:16947529-Humans,
pubmed-meshheading:16947529-Immunosuppressive Agents,
pubmed-meshheading:16947529-Lupus Erythematosus, Systemic,
pubmed-meshheading:16947529-Lymphocyte Activation,
pubmed-meshheading:16947529-Male,
pubmed-meshheading:16947529-Membrane Potentials,
pubmed-meshheading:16947529-Middle Aged,
pubmed-meshheading:16947529-Mitochondrial Membranes,
pubmed-meshheading:16947529-Sirolimus,
pubmed-meshheading:16947529-T-Lymphocytes
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pubmed:year |
2006
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pubmed:articleTitle |
Rapamycin reduces disease activity and normalizes T cell activation-induced calcium fluxing in patients with systemic lupus erythematosus.
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pubmed:affiliation |
State University of New York, Syracuse, NY 13210, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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