Source:http://linkedlifedata.com/resource/pubmed/id/20140011
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-3-1
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pubmed:abstractText |
Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease. Innate and adaptive immunity cooperatively contribute to the development of SLE. Antigen-presenting cells (APCs) have been suggested to link innate and adaptive immunity. T-cell immunoglobulin- and mucin-domain-containing molecule-4 (Tim-4; also known as Timd4), expressed primarily on the surface of APCs, is a member of the TIM family, a recently described group of molecules that have received much attention as potential regulators of the immune system. In this study, we used quantitative real-time reverse transcription-polymerase chain reaction to examine the mRNA expression of Tim-4 in peripheral blood mononuclear cells (PBMCs) from SLE patients and further analyzed the correlation between the expression of Tim-4 and Tim-1 (a potential ligand for Tim-4) in PBMCs and serum tumor necrosis factor (TNF)-alpha levels. The results showed that Tim-4 mRNA expression in PBMCs was significantly higher in SLE patients than in healthy controls, especially those patients in the active phase of disease. Moreover, Tim-4 mRNA levels were closely correlated with Tim-1 mRNA levels in PBMCs and with serum TNF-alpha levels in SLE patients but not in the control group. Taken together, these results demonstrate that Tim-4 may be involved in the pathogenesis of SLE.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/HAVCR1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Virus,
http://linkedlifedata.com/resource/pubmed/chemical/TIMD4 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
2042-0226
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
152-6
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pubmed:meshHeading |
pubmed-meshheading:20140011-Adolescent,
pubmed-meshheading:20140011-Adult,
pubmed-meshheading:20140011-Child,
pubmed-meshheading:20140011-Female,
pubmed-meshheading:20140011-Gene Expression Regulation,
pubmed-meshheading:20140011-Humans,
pubmed-meshheading:20140011-Leukocytes,
pubmed-meshheading:20140011-Lupus Erythematosus, Systemic,
pubmed-meshheading:20140011-Male,
pubmed-meshheading:20140011-Membrane Glycoproteins,
pubmed-meshheading:20140011-Membrane Proteins,
pubmed-meshheading:20140011-Middle Aged,
pubmed-meshheading:20140011-RNA, Messenger,
pubmed-meshheading:20140011-Receptors, Virus,
pubmed-meshheading:20140011-Tumor Necrosis Factor-alpha,
pubmed-meshheading:20140011-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Increased expression of human T-cell immunoglobulin- and mucin-domain-containing molecule-4 in peripheral blood mononuclear cells from patients with system lupus erythematosus.
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pubmed:affiliation |
Institute of Immunology, Shandong University School of Medicine, Jinan, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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