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Anti-tumor necrosis factor therapies
1The Kennedy Institute Division, Imperial College School of Medicine, London, UK. peter.c.taylor@ic.ac.uk
Current Opinion in Rheumatology
|May 3, 2001
Summary
Biologicals targeting tumor necrosis factor-alpha (TNF-alpha) offer sustained rheumatoid arthritis (RA) symptom improvement and joint protection. Effective and low immunogenicity anti-TNF agents represent a new standard of care for RA patients.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- Long-term use of biologicals targeting tumor necrosis factor-alpha (TNF-alpha) has shown sustained improvement in rheumatoid arthritis (RA) symptoms.
- Efficacy and low immunogenicity are key criteria for successful anti-TNF agents in RA therapy.
Purpose of the Study:
- To evaluate the efficacy of current anti-TNF therapies in rheumatoid arthritis (RA).
- To assess the impact of anti-TNF agents on joint structural damage and disability in RA patients.
Main Methods:
- Review of published studies on infliximab and etanercept regimens for RA.
- Analysis of 1-year data for infliximab and methotrexate combination therapy.
- Evaluation of etanercept's efficacy in early RA compared to methotrexate.
Main Results:
- Infliximab (3 or 10 mg/kg) with methotrexate, and etanercept (25 mg twice weekly) appear to be efficacious and of low immunogenicity.
- Anti-TNF therapy has demonstrated protection of joints from structural damage.
- Combination therapy with infliximab and methotrexate reduced disability in RA patients over 1 year.
- Etanercept showed faster symptom reduction and erosion progression retardation in early RA compared to methotrexate.
Conclusions:
- Anti-TNF therapies, including infliximab and etanercept, establish a new standard for symptom control in both established and early RA.
- These biological agents provide significant joint protection, mitigating structural damage progression.
- The combination of anti-TNF agents with methotrexate offers sustained benefits and reduced disability in RA management.