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Updated: Aug 5, 2026

Experimental Autoimmune Uveitis: An Intraocular Inflammatory Mouse Model
Published on: January 12, 2022
Etanercept therapy in children with treatment-resistant uveitis
1Division of Rheumatology, Children's Hospital Los Angeles, California 90027, USA.
Insights
Etanercept, a tumor necrosis factor fusion protein, shows promise in treating pediatric uveitis resistant to other therapies. This study indicates a beneficial effect, warranting further investigation into optimal administration for chronic uveitis.
Area of Science:
- Ophthalmology
- Rheumatology
- Immunology
Background:
- Uveitis in children, particularly when associated with juvenile rheumatoid arthritis, presents a significant treatment challenge.
- Previous therapies including topical steroids, methotrexate, and cyclosporine were ineffective in the study cohort.
- Tumor necrosis factor (TNF) inhibitors are a class of biologic agents used in autoimmune conditions.
Purpose of the Study:
- To assess the safety and efficacy of etanercept for treating chronic, treatment-resistant uveitis in pediatric patients.
- To determine the impact of etanercept on ocular inflammation and visual acuity in children.
- To explore the effectiveness of different dosing regimens of etanercept.
Main Methods:
- A prospective study involving 10 children (mean age 7.5 years) with chronic active uveitis, many with associated juvenile rheumatoid arthritis.
- Patients had failed prior treatments with conventional immunosuppressants.
- Treatment involved subcutaneous etanercept, initially at 0.4 mg/kg twice weekly, with a potential dose increase if needed.
Main Results:
- Significant reduction in anterior chamber cell density was observed in 63% of affected eyes within 3 months (P = 0.017), with 4 eyes achieving remission.
- Visual acuity improved in 40% of eyes with pre-existing visual impairment (<20/25).
- Ocular side effects were minimal, with only one child experiencing uveitis exacerbation; other ocular parameters remained stable.
Conclusions:
- Subcutaneous etanercept demonstrates a beneficial effect in children with treatment-resistant chronic uveitis.
- The drug appears safe and effective for this pediatric population.
- Further controlled studies are needed to confirm efficacy and establish optimal systemic or topical administration routes for etanercept.
Objective:
To evaluate the safety and efficacy of the tumor necrosis factor fusion protein etanercept in children with treatment-resistant uveitis.
Methods:
Ten children with chronic active uveitis (7 girls and 3 boys, mean age 7.5 years [range 3-12 years]) were enrolled in this prospective study. In 7 children, uveitis was associated with pauciarticular juvenile rheumatoid arthritis. Five children were antinuclear antibody positive. All patients had failed previous therapy with topical steroids and methotrexate and/or cyclosporine. All were treated with etanercept at a dosage of 0.4 mg/kg twice weekly for the first 3 months, and then, if eyes did not improve, with 25 mg twice weekly (mean 1.1 mg/kg) for at least 3 additional months.
Results:
At the beginning of the trial, uveitis affected 18 eyes in the 10 children. Within 3 months, 10 of 16 affected eyes (63%; P = 0.017) showed a rapid decrease in anterior chamber cell density, including remission of uveitis in 4 eyes. In children with visual acuity of less than 20/25, 4 of 10 eyes (40%) improved. An exacerbation of uveitis during etanercept therapy occurred in only 1 child (1 of 14 eyes [7%]). Other ocular outcome parameters, such as intraocular pressure, synechia formation, and lens clarity, remained unchanged. Following a dosage increase to an average of 1.1 mg/kg after 3 months in 7 children, no further improvement was noted.
Conclusion:
Our data suggest that etanercept injected subcutaneously twice a week has a beneficial effect on treatment-resistant chronic uveitis in children. Further controlled studies with etanercept in systemic or topical form are necessary to confirm its efficacy and optimal mode of administration.
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