Lack of Evidence of Stimulatory Autoantibodies to Platelet-Derived Growth Factor Receptor in Patients With Systemic Sclerosis

被引:73
作者
Classen, Jean-Francois
Henrohn, Dan [2 ]
Rorsman, Fredrik [2 ]
Lennartsson, Johan [3 ]
Lauwerys, Bernard R. [4 ]
Wikstrom, Gerhard [2 ]
Rorsman, Charlotte [3 ]
Lenglez, Sandrine
Franck-Larsson, Karin [2 ]
Tomasi, Jean-Paul [4 ]
Kampe, Olle [2 ]
Vanthuyne, Marie [4 ]
Houssiau, Frederic A. [4 ]
Demoulin, Jean-Baptiste [1 ]
机构
[1] Catholic Univ Louvain, MEXP Unit, de Duve Inst, B-1200 Brussels, Belgium
[2] Univ Uppsala Hosp, Uppsala, Sweden
[3] Uppsala Univ, Ludwig Inst Canc Res, Uppsala, Sweden
[4] Catholic Univ Louvain, St Luc Univ Hosp, B-1200 Brussels, Belgium
来源
ARTHRITIS AND RHEUMATISM | 2009年 / 60卷 / 04期
关键词
PDGF RECEPTOR; ANGIOTENSIN-II; TRANSACTIVATION; BETA; CLASSIFICATION; SCLERODERMA; CHEMOTAXIS; FIBROSIS; TYROSINE; KINASE;
D O I
10.1002/art.24381
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Systemic sclerosis (SSc) is a severe connective tissue disease of unknown etiology, characterized by fibrosis of the skin and multiple internal organs. Recent findings suggested that the disease is driven by stimulatory autoantibodies to platelet-derived growth factor receptor (PDGFR), which stimulate the production of reactive oxygen species (ROS) and collagen by fibroblasts. These results opened novel avenues of research into the diagnosis and treatment of SSc. The present study was undertaken to confirm the presence of anti-PDGFR antibodies in patients with SSc. Methods. Immunoglobulins from 37 patients with SSc were purified by protein A/G chromatography. PDGFR activation was tested using 4 different sensitive bioassays, i.e., cell proliferation, ROS production, signal transduction, and receptor phosphorylation; the latter was also tested in a separate population of 7 patients with SSc from a different research center. Results. Purified IgG samples from patients with SSc were positive when tested for antinuclear autoantibodies, but did not specifically activate PDGFR alpha or PDGFR beta in any of the tests. Cell stimulation with PDGF itself consistently produced a strong signal. Conclusion. The present results raise questions regarding the existence of agonistic autoantibodies to PDGFR in SSc.
引用
收藏
页码:1137 / 1144
页数:8
相关论文
共 32 条
[1]   c-Jun N-terminal kinase is necessary for platelet-derived growth factor-mediated chemotaxis in primary fibroblasts [J].
Amagasaki, Kenichi ;
Kaneto, Hideaki ;
Heldin, Carl-Henrik ;
Lennartsson, Johan .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (31) :22173-22179
[2]  
Andrews A, 1999, INVEST OPHTH VIS SCI, V40, P2683
[3]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[4]   Is scleroderma an autoantibody mediated disease? [J].
Arnett, Frank C. .
CURRENT OPINION IN RHEUMATOLOGY, 2006, 18 (06) :579-581
[5]   Anti-PDGFR-α antibodies measured by non-bioactivity assays are not specific for systemic sclerosis [J].
Balada, E. ;
Simeon-Aznar, C. P. ;
Ordi-Ros, J. ;
Rosa-Leyva, M. ;
Selva-O'Callaghan, A. ;
Pardos-Gea, J. ;
Fonollosa-Pla, V. ;
Vilardell-Tarres, M. .
ANNALS OF THE RHEUMATIC DISEASES, 2008, 67 (07) :1027-1029
[6]  
Baroni SS, 2006, NEW ENGL J MED, V354, P2667
[7]   Autoantibodies in systemic sclerosis and fibrosing syndromes: clinical indications and relevance [J].
Cepeda, EJ ;
Reveille, JD .
CURRENT OPINION IN RHEUMATOLOGY, 2004, 16 (06) :723-732
[8]  
Danishevskiy K, 2004, EUR J PUBLIC HEALTH, V14, P16
[9]   Role of insulin receptor substrate-2 in interleukin-9-dependent proliferation [J].
Demoulin, JB ;
Grasso, L ;
Atkins, JM ;
Stevens, M ;
Louahed, J ;
Levitt, RC ;
Nicolaides, NC ;
Renauld, JC .
FEBS LETTERS, 2000, 482 (03) :200-204
[10]  
Demoulin JB, 2000, CANCER RES, V60, P3971