Evidence map›Paper›PMID 41230121›Full record

ReviewTherapeutic advances in neurological disorders2025

Chimeric antigen receptor T-cell therapy for stiff-person syndrome: bridging innovation and clinical challenges in neuroimmunology.

Jonathan Wickel, Jeremias Motte, Ilya Ayzenberg, Benjamin Vlad, Ralf Gold, Christian Geis, Simon Faissner

Registry-linked trialAbstract readReview
In one paragraph

Review in Therapeutic advances in neurological disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06588491 (KYSA-8), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT06588491 phase2completednot on this map

KYSA-8: A Phase 2 Open-Label, Single-Arm, Multicenter Study of KYV-101, an Autologous Fully Human Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Treatment Refractory Stiff Person Syndrome

TypeinterventionalSponsorKyverna TherapeuticsRan2024 to 2026Enrolled27ConditionsStiff-Person Syndrome, SPSArmsStandard lymphodepletion regimen
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Jonathan WickelSection Translational Neuroimmunology, Department of Neurology, Jena University Hospital, Jena, Germany.
Jeremias MotteDepartment of Neurology, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.ORCID https://orcid.org/0000-0002-6624-8565
Ilya AyzenbergDepartment of Neurology, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.
Benjamin VladSection Translational Neuroimmunology, Department of Neurology, Jena University Hospital, Jena, Germany.
Ralf GoldDepartment of Neurology, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.ORCID https://orcid.org/0000-0002-7223-3052
Christian GeisSection Translational Neuroimmunology, Department of Neurology, Jena University, Am Klinikum 1, Jena 07747, Germany.
Simon FaissnerDepartment of Neurology, Ruhr-University Bochum, St. Josef-Hospital, Gudrunstr. 56, Bochum 44791, Germany.ORCID https://orcid.org/0000-0002-3412-762X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cells (CAR T-cells) have revolutionized the treatment of hematologic malignancies and are now being explored in autoimmune diseases, including neuroimmunological disorders. The first clinical applications of CAR T-cell therapy for autoimmune diseases have demonstrated promising efficacy, particularly in systemic lupus erythematosus and myasthenia gravis. While CAR T-cell therapy can induce profound B-cell depletion, leading to durable remission, concerns remain regarding cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. However, neuroimmunological conditions with lower target cell burdens may carry a reduced risk of these adverse events. Recent evidence suggests CAR T-cells could offer a transformative approach for stiff-person syndrome (SPS), a rare but debilitating autoimmune neurological disorder characterized by muscle rigidity and spasms. The first reported case of anti-CD19 CAR T-cell therapy in a treatment-refractory SPS patient resulted in substantial clinical improvement, including increased mobility and reduced dependence on symptomatic medication. A newly launched phase II clinical trial (NCT06588491) aims to further evaluate the safety and efficacy of anti-CD19 CAR T-cell therapy in SPS. In this review, we examine the current evidence supporting the use of CAR T-cells in neuroimmunological conditions, discuss the clinical picture and pathophysiological processes associated with stiff person spectrum disorders (SPSD), and elaborate on perspectives and limitations of CAR T-cell therapy in SPSD and beyond.

Indexed as

CARCAR-T cellCD19GADPERMSPSSPSD

Identifiers

PMID41230121
PMCPMC12602911

What OpenQuestion holds

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Registered trials

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.