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Articles Published Processes
9/10/2014 2:59:00 PM | Browse: 951 | Download: 825
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Received |
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2013-07-02 09:49 |
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Peer-Review Started |
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2013-07-02 15:23 |
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To Make the First Decision |
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2013-07-19 08:48 |
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Return for Revision |
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2013-07-20 22:33 |
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Revised |
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2013-07-29 22:00 |
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Second Decision |
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2013-09-13 15:00 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2013-09-13 22:53 |
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Articles in Press |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2013-10-29 16:59 |
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Publish the Manuscript Online |
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2013-11-29 02:07 |
Category |
Immunology |
Manuscript Type |
Minireviews |
Article Title |
Decoy receptor 3: Its role as biomarker for chronic inflammatory diseases
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Manuscript Source |
Invited Manuscript |
All Author List |
Spyros I Siakavellas and Giorgos Bamias |
Funding Agency and Grant Number |
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Corresponding Author |
Giorgos Bamias, MD, Academic Department of Gastroenterology, Ethnikon and Kapodistriakon University, Laikon Hospital, 17 Agiou Thoma Str., 11527 Athens, Greece. gbamias@gmail.com |
Key Words |
Decoy receptor 3; Tumor necrosis factor receptor superfamily of proteins; Chronic inflammation; Infection; Disease activity; Biomarker |
Core Tip |
Members of the tumor-necrosis factor-? (TNF-?) and TNF-? receptor superfamilies play important roles in the function of the immune system. Decoy receptor 3 (DcR3) is a decoy receptor that exists only as soluble protein and has the ability to bind to FasL, LIGHT and TL1A. Recent studies showed that DcR3 is upregulated and may be pathogenetically implicated in systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease and infection. DcR3 may become a useful biomarker for chronic inflammatory disorders, as it is upregulated in response to inflammatory stimuli, and may serve both as a prognostic factor for disease severity and as an indicator of response to treatment. |
Publish Date |
2013-11-29 02:07 |
Citation |
Siakavellas SI, Bamias G. Decoy receptor 3: Its role as biomarker for chronic inflammatory diseases. World J Immunol 2013; 3(3): 44-53 |
URL |
http://www.wjgnet.com/2219-2824/full/v3/i3/44.htm |
DOI |
http://dx.doi.org/10.5411/wji.v3.i3.44 |
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