# Obinutuzumab Treatment in Rituximab- and Bortezomib-Resistant Phospholipase A2 Receptor Antibody-Positive Membranous Nephropathy

**Authors:** Uygar Yildirim, Sultan Ozkurt, Ahmet Ugur Yalcin

PMC · DOI: 10.7759/cureus.104285 · 2026-02-26

## TL;DR

Obinutuzumab helped a patient with resistant kidney disease linked to PLA2R antibodies, improving kidney function and reducing symptoms.

## Contribution

This case suggests obinutuzumab may be effective in treating PLA2R antibody-positive membranous nephropathy resistant to other therapies.

## Key findings

- Obinutuzumab treatment led to rapid and sustained clinical improvement in a patient with resistant PLA2R antibody-positive MN.
- Proteinuria decreased significantly, serum albumin normalized, and renal function recovered following obinutuzumab therapy.
- Complete B-cell depletion with obinutuzumab may overcome resistance to conventional anti-CD20 therapies like rituximab.

## Abstract

Primary membranous nephropathy (MN) is a frequent cause of nephrotic syndrome in adults and is commonly linked to circulating autoantibodies against the M-type phospholipase A2 receptor (PLA2R). Rituximab has proven effective as a B-cell-depleting therapy in many patients; however, a significant proportion eventually develop resistance. We report the case of a 54-year-old man with PLA2R antibody-positive primary MN who did not respond to multiple immunosuppressive therapies, including cyclophosphamide, calcineurin inhibitors, repeated rituximab courses, and bortezomib. Despite ongoing nephrotic syndrome and declining renal function, treatment with obinutuzumab resulted in rapid and sustained clinical improvement. This was associated with a substantial reduction in proteinuria, normalization of serum albumin, and recovery of renal function. Our findings suggest that obinutuzumab may offer an effective therapeutic option for highly refractory PLA2R antibody-positive MN and that achieving more complete B-cell depletion could overcome resistance to conventional anti-CD20 therapy.

## Linked entities

- **Proteins:** PLA2R1 (phospholipase A2 receptor 1)
- **Chemicals:** bortezomib (PubChem CID 387447), cyclophosphamide (PubChem CID 2907)
- **Diseases:** membranous nephropathy (MONDO:0005376), nephrotic syndrome (MONDO:0005377)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PLA2R1 (phospholipase A2 receptor 1) [NCBI Gene 22925] {aka CLEC13C, PLA2-R, PLA2G1R, PLA2IR, PLA2R}
- **Diseases:** nephrotic syndrome (MESH:D009404), MN (MESH:D015433), proteinuria (MESH:D011507)
- **Chemicals:** Obinutuzumab (MESH:C543332), Rituximab (MESH:D000069283), cyclophosphamide (MESH:D003520), Bortezomib (MESH:D000069286)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC13032506