rdf:type |
|
lifeskim:mentions |
umls-concept:C0015980,
umls-concept:C0026769,
umls-concept:C0030705,
umls-concept:C0032105,
umls-concept:C0087111,
umls-concept:C0302350,
umls-concept:C0385242,
umls-concept:C0441889,
umls-concept:C0443252,
umls-concept:C0681842,
umls-concept:C0871261,
umls-concept:C0879626,
umls-concept:C1336646,
umls-concept:C1337092,
umls-concept:C1367714,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
|
pubmed:issue |
1-2
|
pubmed:dateCreated |
2007-10-30
|
pubmed:abstractText |
High serum levels of soluble TRAIL (sTRAIL) before or during the first year of Interferon-beta (IFN-beta) therapy were shown to predict an individual therapeutic response of patients with relapsing-remitting multiple sclerosis (RRMS). Here, we investigated whether sTRAIL plasma levels during long-term IFN-beta treatment correlate with future therapeutic response or adverse effects of treatment. Postinjection short-time bursts of sTRAIL were associated with flu-like symptoms and IP-10/CXCL10 as well as MCP-1/CCL2 induction, and were detected after up to 6 years of continuous IFN-beta therapy. However, neither sTRAIL nor chemokine levels allowed prediction of one- and two-year clinical treatment response in 30 RRMS patients, prospectively followed by blinded investigators.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/CCL2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/CXCL10 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CXCL10,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-beta,
http://linkedlifedata.com/resource/pubmed/chemical/TNF-Related Apoptosis-Inducing...,
http://linkedlifedata.com/resource/pubmed/chemical/TNFSF10 protein, human
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0165-5728
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
190
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
170-6
|
pubmed:meshHeading |
pubmed-meshheading:17884184-Adult,
pubmed-meshheading:17884184-Biological Markers,
pubmed-meshheading:17884184-Chemokine CCL2,
pubmed-meshheading:17884184-Chemokine CXCL10,
pubmed-meshheading:17884184-Female,
pubmed-meshheading:17884184-Humans,
pubmed-meshheading:17884184-Influenza, Human,
pubmed-meshheading:17884184-Interferon-beta,
pubmed-meshheading:17884184-Male,
pubmed-meshheading:17884184-Middle Aged,
pubmed-meshheading:17884184-Multiple Sclerosis, Relapsing-Remitting,
pubmed-meshheading:17884184-Predictive Value of Tests,
pubmed-meshheading:17884184-Prospective Studies,
pubmed-meshheading:17884184-TNF-Related Apoptosis-Inducing Ligand
|
pubmed:year |
2007
|
pubmed:articleTitle |
TRAIL, CXCL10 and CCL2 plasma levels during long-term Interferon-beta treatment of patients with multiple sclerosis correlate with flu-like adverse effects but do not predict therapeutic response.
|
pubmed:affiliation |
Department of Neurology, Julius-Maximilians-University, Josef-Schneider-Strasse 11, Würzburg, Germany. m.buttmann@uni-wuerzburg.de
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
|