Evidence map›Paper›PMID 42726141›Full record

SynthesisNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Efficacy of efgartigimod in the treatment of autoimmune encephalitis: a systematic review.

Ping Tang, Kaiqiang Xiao, Yi He, Liang Wang

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Ping TangDepartment of Neurology, First Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Kaiqiang XiaoDepartment of Neurology, First Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Yi HeDepartment of Neurology, First Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Liang WangDepartment of Neurology, First Affiliated Hospital, Chongqing Medical University, Chongqing, China. wang0128_0@163.com.ORCID http://orcid.org/0000-0002-0606-561X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutoimmune encephalitis (AE) encompasses a group of inflammatory disorders of the brain parenchyma mediated by autoimmune mechanisms. Currently, first-line immunotherapy for AE typically involves corticosteroids, intravenous immunoglobulin, and plasma exchange or immune adsorption. However, a subset of patients shows an inadequate response to these treatments, which are also associated with an increased risk of infection and other potential adverse effects. Efgartigimod, a neonatal Fc receptor (FcRn) antagonist, is primarily approved for treating generalized myasthenia gravis. Preliminary observations suggest that efgartigimod may also exhibit therapeutic potential in AE.

methodsA comprehensive literature search was performed in the PubMed, Web of Science, Embase, and Cochrane Library databases to identify all relevant studies published up to October 30, 2025. The risk of bias in the included studies was evaluated using standardized tools tailored to each study design. Owing to substantial heterogeneity across study designs and outcome measures, a meta-analysis was not deemed feasible; consequently, the findings are synthesized and presented in narrative form.

resultsTwelve studies were included, comprising nine case reports or series, two case control studies, and one cross‑sectional study. A total of 77 patients with AE were enrolled. The majority (76/77) demonstrated significant clinical improvement following efgartigimod treatment, and no serious adverse events were observed.

conclusionEfgartigimod holds potential as a safe and effective adjunctive therapy for AE patients, either as adjunctive treatment after inadequate responses to first-line or second-line therapies or as concomitant add-on therapy combined with first-line treatment.

Indexed as

EncephalitisHashimoto DiseaseHumansTreatment OutcomeAutoimmune encephalitisEfgartigimodSystematic reviewTreatment effect

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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 OpenQuestion graph.