# Combination therapy of ofatumumab and daratumumab in patients with severe anti-NMDA receptor encephalitis

**Authors:** Baojie Wang, Yufeng Chu, Chao Zhang, Shougang Guo

PMC · DOI: 10.3389/fimmu.2025.1681884 · Frontiers in Immunology · 2025-10-27

## TL;DR

A new combination therapy using ofatumumab and daratumumab shows promise in treating severe, treatment-resistant NMDA receptor encephalitis in two patients.

## Contribution

The study introduces a novel combination therapy for refractory NMDA receptor encephalitis with rapid clinical and serological responses.

## Key findings

- Both patients showed significant functional improvement within 12 weeks of treatment.
- NMDAR-IgG levels became undetectable, and B cells and antibody-secreting cells were rapidly depleted.
- Treatment-related adverse events were acceptable, indicating good tolerability.

## Abstract

N-methyl-D-aspartate receptor (NMDAR) antibody encephalitis (NMDARE) is an autoimmune disorder in which approximately 25% of patients develop refractory disease with severe prolonged neurological deficits. Currently, there is no consensus on optimal treatment for NMDARE refractory to first- or second-line therapies. We present two cases of severe refractory NMDARE treated with novel combination therapy of ofatumumab and daratumumab. We describe two adolescent female patients with severe neuropsychiatric manifestations unresponsive to standard first-line therapies, including intravenous methylprednisolone (IVMP) and intravenous immunoglobulins (IVIG). Following 5–6 cycles of ofatumumab and daratumumab combination therapy, both patients achieved significant functional improvement (modified Rankin Scale [mRS] score ≤ 2) within 12 weeks. Serological analysis revealed undetectable NMDAR-IgG levels and rapid depletion of circulating CD19+ B cells and CD38+ antibody-secreting cells (ASCs) within 2 weeks. Treatment-related adverse events were acceptable. This case report demonstrates that combined treatment of ofatumumab and daratumumab therapy is well-tolerated and may represent a novel therapeutic strategy for severe NMDARE. The observed rapid serological and clinical responses highlight its potential efficacy, warranting further investigation in large cohorts.

## Linked entities

- **Proteins:** Grin1 (glutamate receptor, ionotropic, NMDA1 (zeta 1)), CD19 (CD19 molecule), CD38 (CD38 molecule)
- **Chemicals:** methylprednisolone (PubChem CID 6741)
- **Diseases:** anti-NMDA receptor encephalitis (MONDO:0021081)

## Full-text entities

- **Genes:** CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}
- **Diseases:** neuropsychiatric manifestations (MESH:D012877), autoimmune disorder (MESH:D001327), N-methyl-D-aspartate receptor (NMDAR) antibody encephalitis (MESH:D060426), neurological deficits (MESH:D009461)
- **Chemicals:** methylprednisolone (MESH:D008775), ofatumumab (MESH:C527517), daratumumab (MESH:C556306), IVMP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12597730/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12597730/full.md

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Source: https://tomesphere.com/paper/PMC12597730