Fatal Reactivation of Cytomegalovirus Infection after Use of Rituximab for a Post-Transplantation Lymphoproliferative Disorder
- 27 September 2001
- journal article
- letter
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 345 (13) , 1000
- https://doi.org/10.1056/nejm200109273451315
Abstract
Rituximab is a chimeric monoclonal antibody directed against the CD20 antigen expressed on most B cells and is used to treat B-cell non-Hodgkin's lymphoma.1 Recently, rituximab has been used to treat post-transplantation lymphoproliferative disorders, which may occur after solid-organ and bone marrow transplantation; the prognosis associated with these disorders is usually poor, even if the doses of immunosuppressive drugs are reduced. Rituximab induces profound and durable B-cell depletion without a substantial decrease in serum immunoglobulin levels. Viral infection has rarely been reported after the use of this agent. Hepatitis B reactivation,1,2 visceral varicella–zoster infection,3 and pure red-cell aplasia due to chronic parvovirus B19 infection4 have occurred in patients treated with rituximab, but in all these cases, rituximab was combined with chemotherapy. We describe a fatal reactivation of cytomegalovirus infection after rituximab therapy in a patient with a post-transplantation lymphoproliferative disorder.Keywords
This publication has 3 references indexed in Scilit:
- Acute Hepatitis B in a Patient with Antibodies to Hepatitis B Surface Antigen Who Was Receiving RituximabNew England Journal of Medicine, 2001
- Pure red cell aplasia due to parvovirus B19 in a patient treated with rituximabBlood, 2000
- Treatment of Patients With Low-Grade B-Cell Lymphoma With the Combination of Chimeric Anti-CD20 Monoclonal Antibody and CHOP ChemotherapyJournal of Clinical Oncology, 1999