# Efgartigimod combined with rituximab helps improve the symptoms and reduce the use of corticosteroids in patients with MuSK antibody-positive MG: a single case report

**Authors:** Xiujun Zheng, Jing Wang, Tongtong Cai, Houshi Zhou

PMC · DOI: 10.3389/fimmu.2025.1710017 · Frontiers in Immunology · 2026-01-07

## TL;DR

A patient with MuSK antibody-positive myasthenia gravis showed improved symptoms and reduced corticosteroid use when treated with efgartigimod and rituximab.

## Contribution

This case report highlights the potential of combining efgartigimod with rituximab for MuSK antibody-positive MG.

## Key findings

- Efgartigimod combined with rituximab improved symptoms in a MuSK antibody-positive MG patient.
- The treatment allowed for faster tapering of corticosteroids and pyridostigmine.
- The patient achieved minimal symptom expression with this combination therapy.

## Abstract

Myasthenia gravis (MG) is an autoimmune disorder primarily affecting the neuromuscular junction. Muscle-specific receptor tyrosine kinase antibody (MuSK-Ab)-mediated MG often presents with bulbar weakness and is prone to crisis. Currently, conventional treatments show limited efficacy in MuSK-Ab-mediated MG, while rituximab therapy demonstrates favorable outcomes.

We report a case of a patient who initially achieved symptom control with efgartigimod during an acute exacerbation but experienced symptom recurrence after subsequent rituximab treatment. Owing to poor tolerance to pyridostigmine and corticosteroids, and considering the established efficacy of efgartigimod in MuSK-Ab-positive MG, we opted for continued efgartigimod infusions. This approach quickly improved symptoms, achieved minimal symptom expression (MSE), and allowed faster tapering of corticosteroids and pyridostigmine.

While multiple studies have demonstrated the efficacy and safety of efgartigimod, large-scale studies remain necessary to further evaluate the feasibility of combination therapy with rituximab in MuSK-Ab-positive MG.

## Linked entities

- **Proteins:** MUSK (muscle associated receptor tyrosine kinase)
- **Chemicals:** pyridostigmine (PubChem CID 4991)
- **Diseases:** Myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Genes:** MUSK (muscle associated receptor tyrosine kinase) [NCBI Gene 4593] {aka CMS9, FADS}
- **Diseases:** bulbar weakness (MESH:D018908), MG (MESH:D009157), autoimmune disorder (MESH:D001327)
- **Chemicals:** pyridostigmine (MESH:D011729), rituximab (MESH:D000069283), Efgartigimod (MESH:C000718373)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829326/full.md

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Source: https://tomesphere.com/paper/PMC12829326