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Updated: Jun 27, 2026

Targeted Antibody Blocking by a Dual-Functional Conjugate of Antigenic Peptide and Fc-III Mimetics DCAF
Published on: September 17, 2019
Daratumumab therapy in a pediatric case of C3 nephritic factor-positive proliferative glomerulonephritis with
Sophia Giang1, Anurag K Agrawal2, Aris Oates2
1Department of Pediatrics, University of California, San Francisco, 550 16th Street, 4th Floor, Mailstop: 3214, San Francisco, CA, 94143, USA. sophia.giang@ucsf.edu.
Abstract:
Proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID) is an exceedingly rare cause of glomerulonephritis among children for which prognosis is generally poor, with low incidence of remission and high rates of recurrence after transplant. While there are more cases reported in the adult literature, substantial differences in pediatric vs. adult PGNMID render it essential that we further characterize pediatric cases to optimize management. We report the case of a 12-year-old male presenting initially with edema and hypertension who was subsequently diagnosed with IgG3/Kappa-dominant PGNMID. In the absence of any proven therapy and though without a detectable clone, he was empirically treated with daratumumab with positive effect to date. This is the first reported case of daratumumab monotherapy in pediatric PGNMID, as well as the first PGNMID case to detect presence of C3 nephritic factor.
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