Evidence map›Paper›PMID 41307955›Full record

ArticleJCI insight2026

Cellular immune endophenotypes separating early and late-onset myasthenia gravis.

Jakob Theorell, Nicolas Ruffin, Andrew Fower, Chiara Sorini, Philip Ambrose, Valentina Damato, Lahiru Handunnetthi, Isabel Leite, Sarosh R Irani, Susanna Brauner and 2 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. 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

12 authors.

Jakob TheorellDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Nicolas RuffinDepartment of Clinical Neuroscience, Karolinska Institutet, and Center for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
Andrew FowerNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Chiara SoriniDepartment of Clinical Neuroscience, Karolinska Institutet, and Center for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
Philip AmbroseNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Valentina DamatoDepartment of Neuroscience and Psychology, University of Florence, Florence, Italy.
Lahiru HandunnetthiCentre for Human Genetics, and.
Isabel LeiteNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Sarosh R IraniNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Susanna BraunerDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.
Adam E HandelNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Fredrik PiehlDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The 2 main subgroups of autoimmune myasthenia gravis, a neuromuscular junction disorder associated with muscle weakness, are early- and late-onset forms, defined by onset before or after 50 years of age. Both carry acetylcholine-receptor autoantibodies but differ in sex ratios, genetics, and occurrence of disease-specific thymus inflammation. To distinguish the 2 forms by cellular immune phenotyping, we applied multimodal techniques, including deep spectral cytometric phenotyping and single-cell sequencing. Analysis of 2 independent cohorts identified immunological differences driven by 3 main lymphocyte populations. Lower frequencies of mucosa-associated invariant T cells and naive CD8+ T cells were observed in late-onset myasthenia, suggesting enhanced immune senescence. A highly differentiated, canonical NK cell population was reduced in early-onset myasthenia and negatively correlated with the degree of thymic hyperplasia. Using only the frequency of these 3 populations, correct myasthenia subgroup assignment could be predicted with 90% accuracy. These distinct immunocellular endophenotypes for early- and late-onset disease suggest differences in immunopathogenic processes. Along with demographic factors and other disease subgroup-specific features, the frequency of the identified cell subpopulations may improve clinical classification.

Indexed as

EndophenotypesMyasthenia GravisAdultAgedAge of OnsetAutoantibodiesCD8-Positive T-LymphocytesFemaleHumansKiller Cells, NaturalMaleMiddle AgedReceptors, CholinergicSingle-Cell AnalysisThymus GlandYoung AdultAutoantibodiesReceptors, CholinergicAutoimmunityImmunologyNeuromuscular diseaseNeuroscience

Identifiers

PMID41307955
PMCPMC12890496

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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.