| Literature DB >> 18201220 |
Michael Hertl1, Detlef Zillikens, Luca Borradori, Leena Bruckner-Tuderman, Harald Burckhard, Rüdiger Eming, Andreas Engert, Matthias Goebeler, Silke Hofmann, Nicolas Hunzelmann, Franz Karlhofer, Ocko Kautz, Undine Lippert, Andrea Niedermeier, Martin Nitschke, Martin Pfütze, Marcel Reiser, Christian Rose, Enno Schmidt, Iakov Shimanovich, Michael Sticherling, Sonja Wolff-Franke.
Abstract
Autoimmune bullous skin disorders are induced by autoantibodies against distinct adhesion complexes of the epidermal and dermal-epidermal junction. Since most of these disorders are characterized by a severe, potentially lethal course,they require long-term immunosuppressive treatment to reduce the de novo synthesis of pathogenic autoantibodies by B lymphocytes. Rituximab, a chimeric monoclonal antibody against CD20 on B lymphocytes, has shown promise in several case reports or cohort studies in the treatment of paraneo-plastic pemphigus,refractory cases of pemphigus vulgaris and foliaceus and in other autoimmune bullous disorders. Treatment with rituximab leads to depletion of pathogenic B-cells which may last up to 12 months resulting in a reduction of plasma cells secreting pathogenic autoantibodies. Rituximab is usually administered in an adjuvant setting at a dose of 375 mg/m(2) i.v.in weekly intervals for four consecutive weeks in addition to the standard immunosuppressive treatment. The present consensus statement of German-speaking dermatologists, rheumatologists and oncologists summarizes and evaluates the current evidence for the use and mode of application of rituximab in autoimmune bullous skin disorders.Entities:
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Year: 2008 PMID: 18201220 DOI: 10.1111/j.1610-0387.2007.06602.x
Source DB: PubMed Journal: J Dtsch Dermatol Ges ISSN: 1610-0379 Impact factor: 5.584