Evidence map›Paper›PMID 28026029›Full record

ArticleAnnals of neurology2017

Anti-LGI1 encephalitis is associated with unique HLA subtypes.

Tae-Joon Kim, Soon-Tae Lee, Jangsup Moon, Jun-Sang Sunwoo, Jung-Ick Byun, Jung-Ah Lim, Yong-Won Shin, Jin-Sun Jun, Han Sang Lee, Woo-Jin Lee and 8 more

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Article in Annals of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 3 pooled it
12.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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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

97 citing papers in PubMed, 3 syntheses or guidelines pooled it, 192 citations in OpenAlex.

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  12. Predictors for identifying autoimmune encephalitis in pediatric patients.Frontiers in cellular and infection microbiology · 2026
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  18. Autoimmune encephalitis.Nature reviews. Disease primers · 2025
    Review
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  20. Article

37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Tae-Joon KimDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Soon-Tae LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Jangsup MoonDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Jun-Sang SunwooDepartment of Neurology, Soonchunhyang University Seoul Hospital, Seoul, South Korea.
Jung-Ick ByunDepartment of Neurology, Kyung Hee University Hospital at Gangdong, Seoul, South Korea.
Jung-Ah LimDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Yong-Won ShinDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Jin-Sun JunDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Han Sang LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Woo-Jin LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Ah Reaum YangDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Yunhee ChoiMedical Research Collaborating Center, Seoul National University Hospital, Seoul, South Korea.
Kyung-Il ParkDepartment of Neurology, Seoul National University Hospital Healthcare System Gangnam Center, Seoul, South Korea.
Keun-Hwa JungDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Ki-Young JungDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Manho KimDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Sang Kun LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Kon ChuDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Seoul National University Hospital · KRKyung Hee University Hospital at Gangdong · KRSeoul National University · KRSoonchunhyang University Hospital Seoul · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAutoimmune encephalitis (AE), represented by anti-leucine-rich glioma-inactivated 1 (anti-LGI1) and anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis, has increasing clinical significance based on recent discoveries of neuronal autoantibodies. However, its immunopathogenesis is not fully understood. Here, we investigated whether AE is associated with the human leukocyte antigen (HLA) subtypes.

methodsWe compared the HLA genotypes of 11 anti-LGI1 and 17 anti-NMDAR encephalitis patients to the control groups, which consisted of 210 epilepsy patients and 485 healthy Koreans.

resultsAnti-LGI1 encephalitis was associated with the DRB1*07:01-DQB1*02:02 haplotype (10 patients; 91%) in HLA class II genes, as well as with B*44:03 (8 patients; 73%) and C*07:06 (7 patients; 64%) in the HLA class I region. The prevalence of these alleles in anti-LGI1 encephalitis was significantly higher than that in the epilepsy controls or healthy controls. By contrast, anti-NMDAR encephalitis was not associated with HLA genotypes. Additional analysis using HLA-peptide binding prediction algorithms and computational docking underpinned the close relationship.

interpretationThis finding suggests that most anti-LGI1 encephalitis develops in a population with specific HLA subtypes, providing insight into a novel disease mechanism. Ann Neurol 2017;81:183-192.

Indexed as

AdolescentAdultAgedAnti-N-Methyl-D-Aspartate Receptor EncephalitisAutoantibodiesEncephalitisFemaleHaplotypesHLA-DQ beta-ChainsHLA-DRB1 ChainsHumansIntracellular Signaling Peptides and ProteinsMaleMiddle AgedProteinsYoung AdultAutoantibodiesHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DRB1 ChainsIntracellular Signaling Peptides and ProteinsLGI1 protein, humanProteins

Identifiers

PMID28026029
OpenAlexW2561303015

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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.