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Rheumatology Advance Access originally published online on January 17, 2006
Rheumatology 2006 45(7):842-846; doi:10.1093/rheumatology/kel004
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© The Author 2006. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Rituximab treatment for glomerulonephritis in HCV-associated mixed cryoglobulinaemia: efficacy and safety in the absence of steroids

L. Quartuccio, G. Soardo1, G. Romano, F. Zaja2, C. A. Scott3, G. De Marchi, M. Fabris, G. Ferraccioli4 and S. De Vita

Rheumatology Clinic, DPMSC, 1 Internal Medical Clinic, DPMSC, 2 Hematology Clinic, DPMSC, 3 Institute of Pathology, DRMM, University of Udine, and 4 Rheumatology Clinic, Catholic University of Sacred Heart, Rome, Italy.

Correspondence to: S. De Vita, Rheumatology Clinic, University of Udine, Piazzale Santa Maria della Misericordia 1, 33100 Udine, Italy. E-mail: salvatore.devita{at}med.uniud.it

Objective. Rituximab, an anti-CD20 monoclonal antibody, has been used in lupus nephritis and membranous idiopathic nephropathy and has proved effective in non-renal manifestations of type II mixed cryoglobulinaemia (MC) syndrome. We investigated the possible efficacy and safety of rituximab in the treatment of cryoglobulinaemic nephritis.

Methods. Five patients with active, biopsy-proven, glomerulonephritis in hepatitis C virus (HCV)-related type II MC syndrome were treated with four weekly infusions of rituximab (375 mg/m2) in monotherapy, without steroids whenever possible. Rituximab was the first-line therapy in three cases.

Results. A rapid and sustained renal response was observed in all patients, in one of them without retreatment up to the last follow-up (month 21+). Renal biopsy was repeated after 6 months in one patient and histopathological improvement was documented. Three patients relapsed, at months +5, +7 and +12 of follow-up, respectively. Two of them were then retreated with rituximab and again presented a rapid improvement in renal function. Maintenance therapy with rituximab was performed in two patients: nephritis remission was maintained in both. Fc-{gamma} receptor 3a (Fc{gamma}RIIIa) genotype characterization was consistent with the clinical response observed. Rituximab also proved effective against other active MC manifestations, when present. No major side-effects occurred and steroids were not required in the follow-up.

Conclusions. Rituximab may provide effective and safe therapy in type II MC-related glomerulonephritis, possibly as first-line therapy, avoiding steroids and hazardous immunosuppressive treatment.

KEY WORDS: Cryoglobulinaemia, Nephritis, Rituximab, Steroid


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