Evidence map›Paper›PMID 40131535›Full record

ArticleJournal of neurology2025

Intravenous immunoglobulin as first-line acute treatment in adults with autoimmune encephalitis caused by antibodies to NMDAR, LGI1 and CASPR2.

Joyce Christin Rittel, Dominica Hudasch, Kathrin Doppler, Florian Then Bergh, Martin Lesser, Orhan Aktas, Michael Nagel, Hagen B Huttner, Kevin Rostasy, Simone Tauber and 22 more

Abstract read
In one paragraph

Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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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

32 authors.

Joyce Christin Rittel *Department of Neurology, Hannover Medical School, Hannover, Germany.
Dominica Hudasch *Department of Neurology, Hannover Medical School, Hannover, Germany.
Kathrin DopplerDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany.
Florian Then BerghDepartment of Neurology, University of Leipzig, Leipzig, Germany.
Martin LesserDepartment of Neurology, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Orhan AktasDepartment of Neurology, Medical Faculty and University Hospital, Heinrich-Heine-Universität Düsseldorf, 40225, Düsseldorf, Germany.
Michael NagelDepartment of Neurology, Hospital Osnabrück, Osnabrück, Germany.
Hagen B HuttnerDepartment of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany.
Kevin RostasyPediatric Neurology, Children's Hospital Datteln, University Witten/Herdecke, Witten, Germany.
Simone TauberDepartment of Neurology, RWTH University Hospital, Aachen, Germany.
Manuel A FrieseInstitute of Neuroimmunology and Multiple Sclerosis, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Michael MalterDepartment of Neurology, Faculty of Medicine, University of Cologne and University Hospital of Cologne, Cologne, Germany.
Marie MadlenerDepartment of Neurology, Faculty of Medicine, University of Cologne and University Hospital of Cologne, Cologne, Germany.
Andrea KraftDepartment of Neurology, Martha-Maria Hospital Halle-Dölau, Halle-Dölau, Germany.
Frank HoffmannDepartment of Neurology, Martha-Maria Hospital Halle-Dölau, Halle-Dölau, Germany.
Jan LewerenzDepartment of Neurology, University of Ulm, Ulm, Germany.
Makbule SenelDepartment of Neurology, University of Ulm, Ulm, Germany.
Jonathan WickelSection of Translational Neuroimmunology, Department of Neurology, Jena University Hospital, Jena, Germany.
Christian GeisSection of Translational Neuroimmunology, Department of Neurology, Jena University Hospital, Jena, Germany.
Andreas MoserDepartment of Neurology, University of Lübeck and University Medical Center of Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Klaus-Peter WandingerDepartment of Neurology, University of Lübeck and University Medical Center of Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Thorsten BartschDepartment of Neurology, Kiel University, Kiel, Germany.
Frank LeypoldtDepartment of Neurology, Kiel University, Kiel, Germany.
Franziska ThalerInstitute of Clinical Neuroimmunology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.
Tania KümpfelInstitute of Clinical Neuroimmunology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.
Sven MeuthDepartment of Neurology, Medical Faculty and University Hospital, Heinrich-Heine-Universität Düsseldorf, 40225, Düsseldorf, Germany.
Nico MelzerDepartment of Neurology, Medical Faculty and University Hospital, Heinrich-Heine-Universität Düsseldorf, 40225, Düsseldorf, Germany.
Carsten FinkeDepartment of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Harald PrüssDepartment of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Martin StangelDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Kurt-Wolfram SühsDepartment of Neurology, Hannover Medical School, Hannover, Germany. Suehs.Kurt-Wolfram@mh-hannover.de.ORCID http://orcid.org/0000-0002-8077-481X
German Network for Research on Autoimmune Encephalitis (GENERATE)

Funding

Bundesministerium für Bildung und Forschung 01GM1908ABundesministerium für Bildung und Forschung 01GM2208
6 · The paper itself

Abstract

BACKGROUND AND

objectivesCorticosteroids or plasma exchange are recommended for acute treatment of autoimmune encephalitis (AE). Intravenous immunoglobulins (IVIG) are suggested as an additional treatment option but data on treatment effect is scarce. The objective of the present study was to investigate the impact of the first-line treatment on the three most common forms of AE, in particular, to evaluate the effect of IVIG therapy in these diseases.

methodsA total of 1274 patients from the German Network for Autoimmune Encephalitis Research (GENERATE) were analyzed, and 388 patients were included in the study because they had either anti-NMDAR, anti-LGI1 or anti-CASPR2 antibodies and firs-line immunotherapy (ivMP monotherapy, ivMP + IVIG, ivMP + PE or ivMP + IVIG + PE) or no immunotherapy at all. For the statistical analyses, patients were stratified according to antibody type, distinguishing between anti-NMDAR (IgG1) and anti-LGI1 as well as anti-CASPR2 (predominantly IgG4). The primary endpoint was the clinical outcome at discharge, which was assessed using the modified Rankin Scale (mRS). The mRS scores were then compared between the different treatment groups over time, and the factors influencing the reduction in mRS at discharge were analyzed. Furthermore, a specific investigation was conducted to determine the differences in outcomes between patients treated with ivMP + IVIG and ivMP + PE, each split by antibody subtype.

resultsIn all treatment groups analyzed, significant improvements were observed at the time of discharge and after 12 months compared to disease onset, regardless of the type of first-line treatment. In untreated patients a significant improvement was not observed. The choice of IVIG or PE as an additional treatment to ivMP for anti-NMDAR encephalitis did not affect the primary outcome. In anti-LGI1 or anti-CASPR2 encephalitis, no influence on the primary outcome was observed when IVIG or PE was administered in addition to ivMP, too. However, a direct comparison of the individual antibody subgroups' mRS reductions, depending on the treatment approach (ivMP + IVIG vs. ivMP + PE), revealed that a more significant mRS reduction was observed with ivMP + PE in anti-NMDAR encephalitis. DISCUSSION: The retrospective data give evidence that there is no difference in outcome for the use of ivMP + PE over ivMP + IVIG or vice versa in the treatment of encephalitis caused by antibodies against NMDAR, LGI1 or CASPR2. Furthermore, the specific method of plasma exchange, whether plasmapheresis or immunoadsorption, did not affect the mRS at discharge.

Indexed as

AutoantibodiesEncephalitisHashimoto DiseaseImmunoglobulins, IntravenousImmunologic FactorsMembrane ProteinsNerve Tissue ProteinsProteinsReceptors, N-Methyl-D-AspartateAdultAgedFemaleHumansIntracellular Signaling Peptides and ProteinsMaleMiddle AgedAutoantibodiesCNTNAP2 protein, humanImmunoglobulins, IntravenousImmunologic FactorsIntracellular Signaling Peptides and ProteinsLGI1 protein, humanMembrane ProteinsNerve Tissue ProteinsProteinsReceptors, N-Methyl-D-AspartateAutoimmune encephalitisCASPR2ImmunotherapyIVIGLGI-1NMDA

Identifiers

PMID40131535
PMCPMC11937155

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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.