After more than 10 years of use, rituximab has proven to be remarkably safe. However, accumulated evidence now suggests that under some circumstances it may significantly increase the risk of infections. This risk is difficult to quantify because of confounding factors (namely, concomitant use of immunosuppressive or chemotherapeutic agents and underlying conditions), as well as under-reporting. Increased number of infections has been documented in patients treated with maintenance rituximab for low-grade lymphoma and in patients with concomitant severe immunodeficiency, whether caused by human immunodeficiency virus (NW) infection or immunosuppressive agents like fludarabine. From the practical standpoint, the most important infection is hepatitis B reactivation, which may be delayed and result in fulminant liver failure and death. Special care should be placed on screening for hepatitis B virus (HBV) and preemptive antiviral treatment. Some investigators have reported an increase in Pneumocystis pneumonia. Finally, there is increasing evidence of a possible association with progressive multifocal leukoencephalopathy (PML), a lethal encephalitis caused by the polyomavirus JC. This review enumerates the described infectious complications, summarizes the possible underlying mechanisms of the increased risk, and makes recommendations regarding prevention, diagnosis and management. Semin Hematol 47:187-198. (C) 2010 Published by Elsevier Inc.
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Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Hauser, Stephen L.
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Waubant, Emmanuelle
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Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Waubant, Emmanuelle
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Arnold, Douglas L.
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McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada
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Arnold, Douglas L.
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Vollmer, Timothy
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Antel, Jack
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Bar-Or, Amit
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Panzara, Michael
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Panzara, Michael
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Sarkar, Neena
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Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Hauser, Stephen L.
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Waubant, Emmanuelle
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Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Waubant, Emmanuelle
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Arnold, Douglas L.
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McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada
NeuroRx Res, Montreal, PQ, CanadaUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Arnold, Douglas L.
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Vollmer, Timothy
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Barrow Neurol Clin, Phoenix, AZ USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Vollmer, Timothy
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Antel, Jack
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Fox, Robert J.
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Cleveland Clin, Mellen Ctr Multiple Sclerosis, Cleveland, OH 44106 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Fox, Robert J.
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Bar-Or, Amit
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McGill Univ, Montreal Neurol Inst, Montreal, PQ, CanadaUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Bar-Or, Amit
;
Panzara, Michael
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Biogen Idec Inc, Cambridge, MA USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Panzara, Michael
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Sarkar, Neena
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Sarkar, Neena
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Agarwal, Sunil
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
Agarwal, Sunil
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Langer-Gould, Annette
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Langer-Gould, Annette
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Smith, Craig H.
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA