Rituximab failure vs anakinra success in same patient
Eiling E, et al.
J Am Acad Dermatol 57(2):361-4 · 2007
Grade Ccase reportn=1eng
Abstract
Schnitzler syndrome is a rare disease characterized by a chronic urticarial rash and a monoclonal gammopathy. The exact pathogenesis is still uncertain and treatment remains a challenge. Here, we report a patient who was only recently given the diagnosis of Schnitzler syndrome although the typical symptoms had been present for about 6 years. Administration of the B-cell antibody rituximab did not exert any beneficial effect despite effective elimination of B cells and a reduction of the paraprotein. In contrast, injection of the interleukin-1-receptor antagonist anakinra caused a complete remission within a few days.
Key Findings
- ●Rituximab failure despite B-cell elimination and paraprotein reduction
- ●Complete remission with anakinra within days
- ●Proved disease is inflammation-driven, not antibody-driven
Subject Classification
Antibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedDrug Therapy, CombinationGlucocorticoidsHumansImmunologic FactorsInjections, SubcutaneousInterleukin 1 Receptor Antagonist ProteinMaleMiddle AgedPrednisoloneReceptors, Interleukin-1RetreatmentRituximabSchnitzler SyndromeTime FactorsTreatment FailureTreatment Outcome
Referenced in (1 disease)
ID: pmid-17467852DOI: 10.1016/j.jaad.2006.08.066PMID: 17467852