Evidence mapPaperPMID 41806280Full record

ReviewAdvances in therapy2026

The Treatment of Antibody-Mediated Encephalitis: Current, Future Therapies, Unmet Need and Patient Management.

Smaila Mulic-Al Bunni, Markus Gschwind, Sebastian Finkener, Adam Al-Diwani, Ava Easton, Adam E Handel, Sophie N M Binks

Abstract readReview
In one paragraph

Review in Advances in therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Smaila Mulic-Al BunniOxford Autoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Markus GschwindDepartment of Neurology, Kantonsspital Aarau, Aarau, Switzerland.
Sebastian FinkenerDepartment of Neurology, Kantonsspital Aarau, Aarau, Switzerland.
Adam Al-DiwaniDepartment of Psychiatry, University of Oxford, Oxford, UK.
Ava EastonEncephalitis International, Malton, UK.
Adam E HandelOxford Autoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Sophie N M BinksOxford Autoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK. sophie.binks@ndcn.ox.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past two decades, significant advances have been made in the characterisation of autoimmune encephalitis, its pathophysiology, and the associated autoantibodies. Given the lack of robust clinical trials, the choice of therapy is principally based on observational studies and expert consensus. Current management strategies include immunotherapy, removal of immunological triggers such as tumours when present, and symptomatic treatment of seizures and psychiatric manifestations. With an improved understanding of the underlying pathogenic mechanisms in this rapidly evolving field, the pharmacological treatment of autoimmune encephalitis has evolved over the years, now encompassing various novel therapeutic targets, particularly in the context of third-line immunotherapies. These modalities include B cell depletion, cytokine-targeted therapies, plasma cell-depleting agents, interventions aimed at intrathecal immune cells or their trafficking across the blood-brain barrier, and blockade of the neonatal Fc receptor. This article reviews both established and novel therapeutic approaches for autoimmune encephalitis, with a focus on disease associated with neural surface antibodies, covering immunotherapy and symptomatic management. Additionally, we discuss the unmet needs of patients and the burden of care within this population.

Indexed as

EncephalitisHashimoto DiseaseImmunotherapyAutoantibodiesHumansAutoantibodiesAntibodiesAutoimmuneCarer burdenEncephalitisImmunotherapyLeucine-rich glioma-inactivated 1 (LGI1)NeuropsychiatryN-Methyl-d-aspartate receptor (NMDAR)SeizuresTrials

Identifiers

PMID41806280
PMCPMC13156142

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.