Evidence map›Paper›PMID 39276207›Full record

SynthesisJournal of neurology2024

Chimeric antigen receptor T-cell therapy for autoimmune diseases of the central nervous system: a systematic literature review.

Agni M Konitsioti, Harald Prüss, Sarah Laurent, Gereon R Fink, Christoph Heesen, Clemens Warnke

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  4. Review
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  11. Progressive multiple sclerosis: Evaluating current therapies and exploring future treatment strategies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  12. Targeting human plasma cells using regulated BCMA CAR T cells eliminates circulating antibodies in humanized mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  13. Review
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

6 authors.

Agni M KonitsiotiDepartment of Neurology, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany. agni.konitsioti@uk-koeln.de.
Harald PrüssDepartment of Neurology and Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Sarah LaurentDepartment of Neurology, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.
Gereon R FinkDepartment of Neurology, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.ORCID http://orcid.org/0000-0002-8230-1856
Christoph HeesenDepartment of Neurology, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
Clemens WarnkeDepartment of Neurology, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany. clemens.warnke@uk-koeln.de.ORCID http://orcid.org/0000-0002-3510-9255

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceB-cell-targeting monoclonal antibodies have demonstrated safety and efficacy in multiple sclerosis or anti-aquaporin-4 IgG positive neuromyelitis optica spectrum disorder. However, these therapies do not facilitate drug-free remission, which may become possible with cell-based therapies, including chimeric antigen receptor (CAR) T cells. CAR T-cell therapy holds promise for addressing other antibody-mediated CNS disorders, e.g., MOG-associated disease or autoimmune encephalitis.

objectiveTo provide an overview of the current clinical knowledge on CAR T-cell therapy in central nervous system autoimmunity. EVIDENCE REVIEW: We searched PubMed, Embase, Google Scholar, PsycINFO, and clinicaltrials.gov using the terms 'CAR T cell' and 'multiple sclerosis/MS' or 'neuromyelitis optica/spectrum diseases/NMOSD' or 'MOG-associated disease/MOGAD 'or' autoimmune encephalitis' or 'neuroimmunology'.

findingsAn ongoing phase I clinical trial has indicated the safety and benefits of anti-BCMA CAR T cells in 12 patients with AQP4-IgG seropositive neuromyelitis optica spectrum disorder. Case reports involving two individuals with progressive multiple sclerosis and one patient with stiff-person syndrome demonstrated a manageable safety profile following treatment with anti-CD19 CAR T cells. Recruitment has commenced for two larger studies in MS, and a phase I open-label basket study is underway to evaluate BCMA-directed CAR T cells in various antibody-associated inflammatory diseases, including MOG-associated disease. Preclinical research on NMDA receptor antibody autoimmune encephalitis treated with chimeric autoantibody receptor T cells generated promising data. CONCLUSIONS AND RELEVANCE: There is minimal evidence of the benefits of CAR T-cell therapy in individuals with central nervous system-directed autoimmunity. Nevertheless, multicenter controlled clinical trials with a manageable safety profile appear feasible and are warranted due to very promising case experiences.

Indexed as

Autoimmune Diseases of the Nervous SystemImmunotherapy, AdoptiveReceptors, Chimeric AntigenHumansT-LymphocytesReceptors, Chimeric AntigenAntibody-mediated CNS disordersCAR T-cell therapyCentral nervous system autoimmunityMultiple sclerosisNMOSD

Identifiers

PMID39276207
PMCPMC11446985

What OpenQuestion holds

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Registered trials

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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.