Review summarizes resistance mechanisms and new therapeutic strategies for membranous nephropathy, indicating important clinical implications.
Membranous nephropathy (MN) is an autoimmune disease associated with antibodies against podocyte proteins, and it is the main cause of nephrotic syndrome in adults.Rituximab (RTX) has now become the first-line treatment for membranous nephropathy, with 80% of patients achieving remission.However, some patients develop drug resistance or experience relapse to rituximab, potential resistance mechanisms include: changes in bioavailability and pharmacokinetics; rituximab internalization by B cells; memory B cells escape from rituximab; generation of anti-rituximab antibodies; impact of phospholipase A receptor antibodies and epitope spreading; chronic and irreversible kidney injury.Understanding these specific resistant mechanisms has driven the development of multiple therapies.Emerging treatments, including new generation anti-CD20 monoclonal antibodies, blymphocyte stimulator inhibitors, proteasome inhibitors, complement inhibitors, and plasma cell-targeted drugs, offer new hope for these patients.This review mainly summarizes the potential mechanisms of rituximab resistance in membranous nephropathy and recent therapeutic advances, aiming to provide guidance for clinical management of membranous nephropathy.
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Li et al. (2026) studied this question.
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