Targeting CD38 with Daratumumab in Refractory Systemic Lupus Erythematosus

Lennard Ostendorf(Leibniz Association), Marie E. Burns(Leibniz Association), Pawel Durek(Leibniz Association), Gitta Anne Heinz(Leibniz Association), Frederik Heinrich(Leibniz Association), Panagiotis Garantziotis(Academy of Athens), Philipp Enghard(Humboldt-Universität zu Berlin), Ulrich Richter(Humboldt-Universität zu Berlin), Robert Biesen(Humboldt-Universität zu Berlin), Udo Schneider(Humboldt-Universität zu Berlin), Fabian Knebel(Humboldt-Universität zu Berlin), Gerd R Burmester(Humboldt-Universität zu Berlin), Andreas Radbruch(Leibniz Association), Henrik E. Mei(Leibniz Association), Mir‐Farzin Mashreghi(Leibniz Association), Falk Hiepe(Leibniz Association), Tobias Alexander(Leibniz Association)
New England Journal of Medicine
September 16, 2020
Cited by 313

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.).


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