| Literature DB >> 32937047 |
Lennard Ostendorf1, Marie Burns1, Pawel Durek1, Gitta Anne Heinz1, Frederik Heinrich1, Panagiotis Garantziotis1, Philipp Enghard1, Ulrich Richter1, Robert Biesen1, Udo Schneider1, Fabian Knebel1, Gerd Burmester1, Andreas Radbruch1, Henrik E Mei1, Mir-Farzin Mashreghi1, Falk Hiepe1, Tobias Alexander1.
Abstract
Daratumumab, a human monoclonal antibody that targets CD38, depletes plasma cells and is approved for the treatment of multiple myeloma. Long-lived plasma cells are implicated in the pathogenesis of systemic lupus erythematosus because they secrete autoantibodies, but they are unresponsive to standard immunosuppression. We describe the use of daratumumab that induced substantial clinical responses in two patients with life-threatening lupus, with the clinical responses sustained by maintenance therapy with belimumab, an antibody to B-cell activating factor. Significant depletion of long-lived plasma cells, reduction of interferon type I activity, and down-regulation of T-cell transcripts associated with chronic inflammation were documented. (Supported by the Deutsche Forschungsgemeinschaft and others.).Entities:
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Year: 2020 PMID: 32937047 DOI: 10.1056/NEJMoa2023325
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245