ArticleFrontiers in immunology2025
Efgartigimod in the treatment of Guillain-Barré syndrome: case report.
Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Rapid neurological recovery in Guillain-Barré syndrome treated with efgartigimod.Scientific reports · 2026Article
- Efgartigimod for Guillain-Barré syndrome: rationale, clinical evidence, and future perspectives.Frontiers in immunology · 2026Review
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Guillain-Barré syndrome (GBS) is a rare neurological disorder characterized by muscle weakness and paralysis. Although the exact etiology remains unclear, the current standard treatments include intravenous immunoglobulin (IVIG) and plasma exchange (PLEX) therapy. While the majority of GBS patients respond well to immunotherapy, some severe cases can be fatal. Efgartigimod, an Fc receptor antagonist, has been utilized in the treatment of various autoimmune diseases. However, its clinical efficacy in acute GBS has been rarely documented. In this study, we administered intravenous efgartigimod to four patients with different subtypes of acute GBS, two of whom received efgartigimod monotherapy without concomitant glucocorticoids, IVIG, or PLEX. The treatment outcomes were favorable, suggesting that intravenous efgartigimod may represent a promising therapeutic option for acute GBS. Further research is warranted to validate these preliminary findings.
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