Evidence map›Paper›PMID 35476434›Full record

ArticleScience advances2022

Identification of four novel T cell autoantigens and personal autoreactive profiles in multiple sclerosis.

Mattias Bronge, Klara Asplund Högelin, Olivia G Thomas, Sabrina Ruhrmann, Claudia Carvalho-Queiroz, Ola B Nilsson, Andreas Kaiser, Manuel Zeitelhofer, Erik Holmgren, Mathias Linnerbauer and 19 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% of its field
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. B-cell targeting strategies for the treatment of multiple sclerosis: from non-cellular therapies to CAR-engineered cell therapies.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  3. Immune reconstitution and tolerance-inducing therapies as promising therapeutic approaches in multiple sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  4. Article
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  10. TDP-43 pathology induces CD8bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Antibody reactivity against EBNA1 and GlialCAM differentiates multiple sclerosis patients from healthy controls.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

29 authors at 5 institutions in 2 countries.

Mattias BrongeTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.ORCID 0000-0002-1258-3982
Klara Asplund HögelinNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.
Olivia G ThomasTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.ORCID 0000-0002-2011-1344
Sabrina RuhrmannTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.
Claudia Carvalho-QueirozTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.
Ola B NilssonTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.
Andreas KaiserTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.
Manuel ZeitelhoferDivision of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 171 77 Stockholm, Sweden.
Erik HolmgrenTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.ORCID 0000-0002-2656-1864
Mathias LinnerbauerNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0002-5528-5141
Milena Z AdzemovicNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.
Cecilia HellströmDivision of Affinity Proteomics, Department of Protein Science, SciLifeLab, KTH-Royal Institute of Technology, 171 65 Solna, Sweden.ORCID 0000-0003-0880-5375
Ivan JelcicNeuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zürich, University Hospital Zürich, 8091 Zürich, Switzerland.ORCID 0000-0002-6187-7098
Hao LiuDepartment of Protein Science, KTH-Royal Institute of Technology, 114 21 Stockholm, Sweden.ORCID 0000-0001-6572-2870
Peter NilssonDivision of Affinity Proteomics, Department of Protein Science, SciLifeLab, KTH-Royal Institute of Technology, 171 65 Solna, Sweden.ORCID 0000-0002-4657-8532
Jan HillertDepartment of Clinical Neuroscience, Division of Neurology, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.ORCID 0000-0002-7386-6732
Lou BrundinDepartment of Clinical Neuroscience, Division of Neurology, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.ORCID 0000-0003-4408-7817
Katharina FinkDepartment of Clinical Neuroscience, Division of Neurology, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.
Ingrid KockumNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0002-0867-4726
Katarina TengvallNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0003-0424-3571
Roland MartinNeuroimmunology and MS Research Section (NIMS), Neurology Clinic, University of Zürich, University Hospital Zürich, 8091 Zürich, Switzerland.
Hanna TegelHuman Protein Atlas, Department of Protein Science, KTH-Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-7067-9173
Torbjörn GräslundDepartment of Protein Science, KTH-Royal Institute of Technology, 114 21 Stockholm, Sweden.ORCID 0000-0002-5391-600X
Faiez Al NimerNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0003-0937-5995
André Ortlieb Guerreiro-CacaisNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0002-4561-2823
Mohsen KhademiNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0003-0801-1444
Guro GafvelinTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.ORCID 0000-0003-1618-4011
Tomas OlssonNeuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0002-2938-1877
Hans GrönlundTherapeutic Immune Design, Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, 171 76 Stockholm, Sweden.ORCID 0000-0003-4882-7624
Karolinska Institutet · SEKTH Royal Institute of Technology · SEKarolinska University Hospital · SEUniversity Hospital of Zurich · CHScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory disease of the central nervous system (CNS), in which pathological T cells, likely autoimmune, play a key role. Despite its central importance, the autoantigen repertoire remains largely uncharacterized. Using a novel in vitro antigen delivery method combined with the Human Protein Atlas library, we screened for T cell autoreactivity against 63 CNS-expressed proteins. We identified four previously unreported autoantigens in MS: fatty acid-binding protein 7, prokineticin-2, reticulon-3, and synaptosomal-associated protein 91, which were verified to induce interferon-γ responses in MS in two cohorts. Autoreactive profiles were heterogeneous, and reactivity to several autoantigens was MS-selective. Autoreactive T cells were predominantly CD4

Identifiers

PMID35476434
PMCPMC9045615
OpenAlexW4225101419

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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.