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Etanercept treatment for children with refractory juvenile idiopathic arthritis
Ho-Chang Kuo1, Hong-Ren Yu2, Chih-Chiang Wu1
1Division of Allergy, Immunology and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Kaohsiung, Taiwan.
Insights
Etanercept effectively treated refractory juvenile idiopathic arthritis (JIA) in most patients, improving joint symptoms and reducing inflammation. Conventional therapies were discontinued in responders, though systemic JIA showed less benefit.
Area of Science:
- Rheumatology
- Pediatric Rheumatology
- Immunology
Background:
- Juvenile idiopathic arthritis (JIA) is a chronic autoimmune disease affecting children.
- Refractory JIA cases often require advanced therapeutic strategies.
- Etanercept is a biologic agent targeting tumor necrosis factor-alpha.
Purpose of the Study:
- To evaluate the effectiveness of etanercept in treating juvenile idiopathic arthritis (JIA) refractory to conventional therapies.
- To assess clinical and laboratory outcomes in patients with refractory JIA treated with etanercept.
Main Methods:
- Retrospective analysis of 11 patients with refractory JIA (polyarticular, pauciarticular, systemic types).
- Patients received etanercept (0.4 mg/kg, max 25mg subcutaneously twice weekly) for 12 months.
- Indications included persistent fever, arthritis/arthralgia, or elevated inflammatory markers despite prior treatment.
Main Results:
- 10 out of 11 patients showed significant improvement in arthritis/arthralgia and reduced inflammatory markers (CRP, ESR) at follow-up.
- Mean hemoglobin levels increased, and platelet counts decreased post-treatment.
- Conventional immunosuppressive drugs were discontinued in 10 responders within 2.5 months of etanercept initiation.
Conclusions:
- Etanercept demonstrates significant benefit for polyarticular and pauciarticular JIA refractory to standard treatments.
- Etanercept appears less beneficial for the systemic type of JIA.
- Successful treatment allowed for discontinuation of other immunosuppressive medications in most JIA patients.
Background:
Etanercept has been shown to be an effective treatment for juvenile idiopathic arthritis (JIA). In this study, we evaluated the effectiveness of etanercept therapy in the treatment of refractory JIA.
Methods:
This was a retrospective analysis of 11 patients with refractory JIA (polyarticular type n=7; pauciarticular type, n=2; systemic type, n=2) who received treatment with etanercept during the period 2005-2009 in a medical center. The indications for etanercept treatment included persistent fever, arthritis/arthralgia, or elevated levels of inflammatory mediators after treatment with methotrexate and/or prednisolone for more than 6 months. The patients were treated with etanercept (0.4 mg/kg, with maximal 25mg, subcutaneously, twice a week) for a total of 12 months.
Results:
The degree of arthritis/arthralgia improved (range of motion and painful sensation of involved joints), and the levels of inflammatory markers (C-reactive protein and erythrocyte sedimentation rate) decreased progressively in 10 of the 11 patients (p<0.05) at 1-, 3-, 5-, and 12-month follow-up after treatment with etanercept. Mean hemoglobin levels significantly increased, whereas mean platelet counts decreased after etanercept treatment (p<0.05). Only one patient with systemic type of JIA failed to respond to the treatment after 6 weeks of etanercept therapy. Methotrexate, prednisolone, and other immunosuppressive drugs were successfully discontinued after a mean of 2.5 months (range, 1-5 months) of etanercept therapy in the 10 patients who responded to etanercept treatment.
Conclusion:
Etanercept is beneficial for patients with polyarticular and pauciarticular type of JIA that is refractory to conventional treatment but less beneficial for systemic type of JIA.
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