Rituximab failure vs anakinra success in same patient

Eiling E, et al.

J Am Acad Dermatol 57(2):361-4 · 2007

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)

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  1. passsource metadataJun 1, 2026, 04:40 PMby pubmed-api

    Stored DOI was incorrect; corrected to the PubMed-registered DOI (verified to resolve to this article).

    tools: pubmed.esummary, crossref.works

ID: pmid-17467852DOI: 10.1016/j.jaad.2007.03.036PMID: 17467852