Evidence map›Paper›PMID 28675562›Full record

ReviewEpilepsia2017

Innate and adaptive immunity in human epilepsies.

Jan Bauer, Albert J Becker, Wassim Elyaman, Jukka Peltola, Stephan Rüegg, Maarten J Titulaer, James A Varley, Ettore Beghi

Open access · hybridAbstract readReview
In one paragraph

Review in Epilepsia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
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

48 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Article
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  9. Review
  10. Autoimmune encephalitis-associated epilepsy.Nature reviews. Neurology · 2025
    Review
  11. Article
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  13. Review
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  17. Review
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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

8 authors at 8 institutions in 8 countries.

Jan BauerDepartment of Neuroimmunology, Center for Brain Research Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5802-8047
Albert J BeckerSection for Translational Epilepsy Research, Department of Neuropathology, University of Bonn - Medical Center, Bonn, Germany.
Wassim ElyamanBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, U.S.A.
Jukka PeltolaDepartment Neurology, Tampere University Hospital, Tampere, Finland.
Stephan RüeggDepartment Neurology, University Hospital Basel, Basel, Switzerland.
Maarten J TitulaerDepartment Neurology, Erasmus University Medical Center, Rotterdam, The Netherlands.
James A VarleyNuffield Department Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom.
Ettore BeghiIRCCS-Mario Negri Institute for Pharmacological Research, Milano, Italy.
Broad Institute · USErasmus MC · NLJohn Radcliffe Hospital · GBMario Negri Institute for Pharmacological Research · ITMedical University of Vienna · ATTampere University Hospital · FIUniversity Hospital of Basel · CHUniversity of Bonn · DE

Funding

Austrian Science Fund FWF P 26936
6 · The paper itself

Abstract

Inflammatory mechanisms have been increasingly implicated in the origin of seizures and epilepsy. These mechanisms are involved in the genesis of encephalitides in which seizures are a common complaint. Experimental and clinical evidence suggests different inflammatory responses in the brains of patients with epilepsy depending on the etiology. In general, activation of both innate and adaptive immunity plays a role in refractory forms of epilepsy. Epilepsies in which seizures develop after infiltration of cells of the adaptive immune system in the central nervous system (CNS) include a broad range of epileptic disorders with different (known or unknown) etiologies. Infiltration of lymphocytes is observed in autoimmune epilepsies, especially the classical paraneoplastic encephalitides with antibodies against intracellular tumor antigens. The presence of lymphocytes in the CNS also has been found in focal cerebral dysplasia type 2 and in cortical tubers. Various autoantibodies have been shown to be associated with temporal lobe epilepsy (TLE) and hippocampal sclerosis of unknown etiology, which may be due to the presence of viral DNA. During the last decade, an increasing number of antineuronal autoantibodies directed against membranous epitopes have been discovered and are associated with various neurologic syndromes, including limbic encephalitis. A major challenge in epilepsy is to define biomarkers, which would allow the recognition of patient populations who might benefit from immune-modulatory therapies. Some peripheral inflammatory markers appear to be differentially expressed in patients with medically controlled and medically refractory and, as such, could be used for diagnostic, prognostic, or therapeutic purposes. Establishing an autoimmune basis in patients with drug-resistant epilepsy allows for efficacious and targeted immunotherapy. Although current immunotherapies can give great benefit to the correctly identified patient, there are limitations to their efficacy and they may have considerable side effects. Thus the identification of new immunomodulatory compounds remains of utmost importance.

Indexed as

Adaptive ImmunityAutoantibodiesBiomarkersBrainDrug Resistant EpilepsyEpilepsyHumansImmunity, InnateImmunomodulationImmunotherapyLymphocytesNeuronsAutoantibodiesBiomarkersAdaptive immunityAutoantibodiesEncephalitidesEpilepsyImmunomodulatory drugsInnate immunity

Identifiers

PMID28675562
PMCPMC5535008
OpenAlexW2731939491

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.