Serum protein profile in systemic-onset juvenile idiopathic arthritis differentiates response versus nonresponse to therapy 英文参考文献.docVIP
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Serum protein profile in systemic-onset juvenile idiopathic arthritis differentiates response versus nonresponse to therapy 英文参考文献
Available online /content/7/4/R746
Research article
Open Access
Vol 7 No 4
Serum protein profile in systemic-onset juvenile idiopathic
arthritis differentiates response versus nonresponse to therapy
Takako Miyamae1, David E Malehorn2, Bonnie Lemster1, Masaaki Mori3, Tomoyuki Imagawa3,
Shumpei Yokota3, William L Bigbee2, Manda Welsh2, Klaus Klarskov4, Norihiro Nishomoto5,
Abbe N Vallejo1 and Raphael Hirsch1
1Division of Rheumatology, Childrens Hospital of Pittsburgh, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA
15213
2University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213
3Department of Pediatrics, Yokohama City University School of Medicine, Yokohama, Japan
4Départment de Phamacologie, Faculté de Medicine, Université de Sherbrooke, Québec, Canada
5Osaka University, Osaka, Japan
Corresponding author: Raphael Hirsch, raphael.hirsch@
Received: 20 Jan 2005 Revisions requested: 22 Feb 2005 Revisions received: 26 Feb 2005 Accepted: 28 Feb 2005 Published: 4 Apr 2005
Arthritis Research Therapy 2005, 7:R746-R755 (DOI 10.1186/ar1723)
This article is online at: /content/7/4/R746
? 2005 Miyamae et al.; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/
2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Systemic-onset juvenile idiopathic arthritis (SJIA) is a disease of
unknown etiology with an unpredictable response to treatment.
We examined two groups of patients to determine whether there
are serum protein profiles reflective of active disease and
predictive of response to therapy. The first group (n = 8)
responded to conventional therapy. The second group (n = 15)
responded to an experimental antibody to the IL-6 receptor
(MRA). Paired sera from each patient were
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