Evidence map›Paper›PMID 40583272›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2025

CD19xCD3 T cell engager blinatumomab effective in refractory generalized myasthenic syndromes.

Tobias Ruck, Niklas Huntemann, Menekse Öztürk, Stefanie Schreiber, Stefanie Lichtenberg, Lars Masanneck, Christopher Nelke, Hend Ben Moussa, Thomas Ulrych, Marc Seifert and 3 more

Abstract readCase Reports
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. T cell engagers in autoimmune diseases.Nature reviews. Immunology · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. CD19xCD3 T cell engager shows therapeutic potential for refractory myasthenic syndromes.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  9. 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

13 authors.

Tobias RuckRuhr University Bochum, BG University Hospital Bergmannsheil, Department of Neurology, 44789 Bochum, Germany; BG University Hospital Bergmannsheil, Heimer Institute for Muscle Research, 44789 Bochum, Germany; Department of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany. Electronic address: tobias.ruck@med.uni-duesseldorf.de.
Niklas HuntemannDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Menekse ÖztürkRuhr University Bochum, BG University Hospital Bergmannsheil, Department of Neurology, 44789 Bochum, Germany; BG University Hospital Bergmannsheil, Heimer Institute for Muscle Research, 44789 Bochum, Germany; Department of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Stefanie SchreiberDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany; Department of Neurology, Otto von Guericke University Magdeburg, 39120 Magdeburg, Germany.
Stefanie LichtenbergDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Lars MasanneckDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Christopher NelkeRuhr University Bochum, BG University Hospital Bergmannsheil, Department of Neurology, 44789 Bochum, Germany; BG University Hospital Bergmannsheil, Heimer Institute for Muscle Research, 44789 Bochum, Germany; Department of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Hend Ben MoussaDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Thomas UlrychDepartment of Haematology and Oncology, University Hospital Düsseldorf, and Center for Integrated Oncology Aachen Bonn Cologne, 40225 Düsseldorf, Germany.
Marc SeifertDepartment of Haematology and Oncology, University Hospital Düsseldorf, and Center for Integrated Oncology Aachen Bonn Cologne, 40225 Düsseldorf, Germany.
Dimitrios MougiakakosDepartment of Haematology, Oncology, and Cell Therapy, Otto von Guericke University Magdeburg, 39120 Magdeburg, Germany.
Sascha DietrichDepartment of Haematology and Oncology, University Hospital Düsseldorf, and Center for Integrated Oncology Aachen Bonn Cologne, 40225 Düsseldorf, Germany.
Sven G MeuthDepartment of Neurology, University Hospital and Medical Faculty Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this case series, we report the first off-label use of the CD19xCD3 T cell engager blinatumomab in two patients with generalized myasthenia gravis (MG). Refractory MG remains a major therapeutic challenge, with patients experiencing severe disability and potentially life-threatening crises despite intensive immunotherapy. This study evaluates the clinical efficacy and safety of short-term blinatumomab treatment in two patients with severe, refractory generalized MG. Both individuals had been experiencing persistent disease burden with myasthenic crises leading to severe disability, despite multimodal immunotherapy. Following treatment with blinatumomab, both patients showed rapid and sustained clinical improvements, reflected in significant reductions in MG-specific scores (MG Activities of Daily Living scale, Quantitative MG score, and revised MG Quality of Life-15), further patient-reported outcomes, digital activity markers, and gait analyses. Laboratory findings revealed persistent B cell depletion in patient 1, whereas patient 2 demonstrated clinical improvement and autoantibody reduction despite B cell repopulation by day 106. Both patients experienced grade 1 cytokine release syndrome during initial treatment phases, but no neurotoxicity or severe adverse events were observed. This report underscores the potential of CD19xCD3 T cell engagers as a promising therapeutic approach in severe autoimmune neuroimmunological disorders, warranting further investigation in clinical trials and mechanistic studies.

Indexed as

Antibodies, BispecificAntigens, CD19Myasthenia GravisT-LymphocytesAdultCD3 ComplexFemaleHumansImmunotherapyMiddle AgedQuality of LifeTreatment OutcomeAntibodies, BispecificAntigens, CD19blinatumomabCD3 ComplexBiTEblinatumomabLambert-Eaton myasthenic syndromeLEMSMGmyasthenia gravisneuroimmunologyneuromuscular diseaserefractory MGT cell engager

Identifiers

PMID40583272
PMCPMC12432851

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.