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Anti-tumor necrosis factor therapy in patients with difficult-to-treat lupus nephritis: A prospective series of nine patients
Clinical and Experimental Rheumatology Online, 07/30/09
Matsumura R et al. – Study demonstrates that in intractable lupus nephritis, anti-TNF-α therapy improved urinary protein levels and SLE activity. Although adverse events must be monitored cautiously, it may be possible to use anti-TNF-α therapy as a third-line treatment.
Methods- An investigation of the efficacy and safety of anti-TNF-α therapy for intractable lupus nephritis
- 9 pts with systemic erythematosus who presented with lupus nephritis resistant to steroids and immunosuppressants
- 200 mg/body of infliximab was drip-infused three times
- No changes to other treatments for 3 mo after the start of anti-TNF-α therapy
- Urinary findings, renal function, serum complement, anti-DNA antibody, SLE activity, and AEs were examined for 6 mo after the start of therapy
- 1/9 pts developed pyelonephritis after the first infliximab injection and received no further injections
- Remaining 8 pts received 3 infliximab injections
- Of the 8 pts, urinary protein decreased after anti-TNF-α therapy in 6 pts; SLEDAI improved in 5 pts
- Urinary findings and/or SLE activity improved in 5 pts
- Of the pts whose urinary protein levels decreased after anti-TNF-α therapy, proteinuria recurred 6 mo after therapy in 1 patient
- After anti-TNF-α therapy, proteinuria and the SLEDAI improved
- Therapy related adverse events:
- Therapy was discontinued in 1 pt who developed pyelonephritis
- 1 pt developed decreased blood pressure due to infusion reactions
- In 1 patient in whom the steroid dosage was increased due to poor response to anti-TNF-α therapy, brainstem infarction occurred 4 mo later
- In 1 pt, anti-DNA Ab levels increased after therapy
- but none of the pts had decreased serum complement levels or increased SLE activity
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