TNF and LT binding capacities in the plasma of arthritis patients:: Effect of etanercept treatment in juvenile idiopathic arthritis

被引:0
作者
Gudbrandsdottir, S
Larsen, R
Sorensen, LK
Nielsen, S
Hansen, MB
Svenson, M
Bendtzen, K
Müller, K
机构
[1] Natl Univ Hosp, Rigshosp, Inst Inflammat Res, DK-2100 Copenhagen, Denmark
[2] Glostrup Cty Hosp, Dept Clin Immunol, Copenhagen, Denmark
[3] Rigshosp, Dept Paediat, DK-2100 Copenhagen, Denmark
关键词
juvenile idiopathic arthritis; arthritis; etanercept; Enbrel; TNF; lymphotoxin;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Etanercept (Enbrel(R)) induces a rapid and sustained decline in disease activity in the majority of patients with refractory juvenile idiopathic arthritis (RA). For unknown reasons, however a number of RA patients fail to respond to this therapy. During this treatment neutralisation of tumour necrosis factor (TNF previously termed TNFalpha) and lymphotoxin (LT previously termed TNFbeta) may be mediated by etanercept itself as well as by naturally occurring soluble TNF receptors. In light of this, it was of interest to study the total TNF neutralizing capacity in plasma before and during treatment with etanercept. Results In initial experiments plasma samples from healthy individuals were incubated with etanercept, and spiked with TNF or LT to a final concentration of 1000 pg/mL. Detection of TNF and LT by ELISA was found to be reduced by approximately 50% and 80% respectively, at a concentration of etanercept of 5-500 ng/mL, which is close to the pharmacological plasma concentrations. Plasma samples (n = 80) were then collected from 12 JIA patients (5 with pauciarticular 5 with polyarticular and 2 with the systemic onset type) during treatment with etanercept (0.4 mg/kg twice weekly) for a period of 20.8 (15.6-23.9) months (median, range). The plasma samples were spiked with LT and the inhibition of LT detection in ELISA was measured. In samples obtained 3 months after the start of etanercept, the inhibition of LT detection was augmented [72% (60-85)] compared with pre-treatment samples [16% (0-32)] (p = 0.0039). These findings were confirmed in binding assays using radiolabelled TNF Among patients who responded insufficiently to therapy, reduced LT binding capacity, coinciding with flares of disease activity, was observed. Conclusion We have developed an assay by which LT binding capacity, reflecting the level of free, pharmacologically active etanercept, may be monitored in the blood of patients treated with etanercept. This assay may prove to be useful in guiding dose adjustments in patients with an incomplete response to etanercept.
引用
收藏
页码:118 / 124
页数:7
相关论文
共 18 条
[1]   Mechanisms of disease: Cytokine pathways and joint inflammation in rheumatoid arthritis. [J].
Choy, EHS ;
Panayi, GS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (12) :907-916
[2]  
De Benedetti Fabrizio, 1997, Current Opinion in Rheumatology, V9, P428, DOI 10.1097/00002281-199709000-00009
[3]   Development of anti-TNF therapy for rheumatoid arthritis [J].
Feldmann, M .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (05) :364-371
[4]  
Foerder C., 2002, ANN RHEUM DIS S1, V61, P72
[5]   Serum p55 and p75 tumour necrosis factor receptors as markers of disease activity in juvenile chronic arthritis [J].
Gattorno, M ;
Picco, P ;
Buoncompagni, A ;
Stalla, F ;
Facchetti, P ;
Sormani, MP ;
Pistoia, V .
ANNALS OF THE RHEUMATIC DISEASES, 1996, 55 (04) :243-247
[6]  
Giannini EH, 1997, ARTHRITIS RHEUM, V40, P1202
[7]   Patterns of expression of tumor necrosis factor alpha, tumor necrosis factor beta, and their receptors in synovia of patients with juvenile rheumatoid arthritis and juvenile spondylarthropathy [J].
Grom, AA ;
Murray, KJ ;
Luyrink, L ;
Emery, H ;
Passo, MH ;
Glass, DN ;
Bowlin, T ;
Edwards, C .
ARTHRITIS AND RHEUMATISM, 1996, 39 (10) :1703-1710
[8]   Etanercept - A review of its use in rheumatoid arthritis [J].
Jarvis, B ;
Faulds, D .
DRUGS, 1999, 57 (06) :945-966
[9]  
LOVELL DJ, 2000, NEW ENGL J MED, V16, P810
[10]  
MORELAND LW, 2002, ANN INT MED