Literature DB >> 21401437

The potential risk of infections during (prolonged) rituximab therapy in rheumatoid arthritis.

Ithamar Heber Brinkman1, Mart A F J van de Laar, Tim L Jansen, Eric N van Roon.   

Abstract

INTRODUCTION: Biologicals are a fast expanding group of new drugs and rituximab (RTX) is one of them. Long-term efficacy and safety constantly need addressing as little is known about these factors. In rheumatoid arthritis, RTX it is used for active disease that is not responding to other therapies. Since RTX acts by depleting B-cells, concerns regarding the long-term safety of this drug have been raised. AREAS COVERED: This review covers 10 manuscripts on RTX safety in rheumatoid arthritis published between January 2004 and July 2010. EXPERT OPINION: In present literature RTX appears to be safe for up to five courses. In this review, important drawbacks of current research are discussed. Longer follow-up time is needed to make relevant conclusions on RTX safety with regard to infectious complications. Prolonged RTX therapy causes subsequent B-cell depletion. Eventually, plasma cells disappear, causing hypogammaglobulinemias and subsequent problems in immunity. The formation of new plasma cells is halted due to a lack of B-cells. Attention needs to be focused on the status of immunoglobulins and the role this plays in the occurrence of infections. Until a complete, long-term safety profile of RTX is available, it cannot be considered safe with regard to the incidence of infectious complications.

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Year:  2011        PMID: 21401437     DOI: 10.1517/14740338.2011.562188

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  5 in total

Review 1.  Update on the autoimmune pathology of multiple sclerosis: B-cells as disease-drivers and therapeutic targets.

Authors:  H-Christian von Büdingen; Arumugam Palanichamy; Klaus Lehmann-Horn; Brady A Michel; Scott S Zamvil
Journal:  Eur Neurol       Date:  2015-03-25       Impact factor: 1.710

Review 2.  Infections associated with monoclonal antibody and fusion protein therapy in humans.

Authors:  Florence Uettwiller; Emilie Rigal; Cyrille Hoarau
Journal:  MAbs       Date:  2011-09-01       Impact factor: 5.857

3.  Suppression of innate and adaptive B cell activation pathways by antibody coengagement of FcγRIIb and CD19.

Authors:  Dániel Szili; Marcell Cserhalmi; Zsuzsanna Bankó; György Nagy; David E Szymkowski; Gabriella Sármay
Journal:  MAbs       Date:  2014-04-23       Impact factor: 5.857

4.  Risk of Infection Associated With Subsequent Biologic Agent Use After Rituximab: Results From a National Rheumatoid Arthritis Patient Registry.

Authors:  Leslie R Harrold; George W Reed; Chitra Karki; Robert Magner; Ashwini Shewade; Ani John; Joel M Kremer; Jeffrey D Greenberg
Journal:  Arthritis Care Res (Hoboken)       Date:  2016-12       Impact factor: 4.794

5.  Serious infection risk after 1 year between patients with rheumatoid arthritis treated with rituximab or with a second TNFi after initial TNFi failure: results from The British Society for Rheumatology Biologics Register for Rheumatoid Arthritis.

Authors:  Lucía Silva-Fernández; Diederik De Cock; Mark Lunt; Audrey S Low; Kath D Watson; Deborah P M Symmons; Kimme L Hyrich
Journal:  Rheumatology (Oxford)       Date:  2018-09-01       Impact factor: 7.580

  5 in total

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