Evidence map›Paper›PMID 25230752›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Clinical and serologic parallels to APS-I in patients with thymomas and autoantigen transcripts in their tumors.

Anette S B Wolff, Jaanika Kärner, Jone F Owe, Bergithe E V Oftedal, Nils Erik Gilhus, Martina M Erichsen, Olle Kämpe, Anthony Meager, Pärt Peterson, Kai Kisand and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

  1. High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Aire Mutations and Autoimmune Diseases.Advances in experimental medicine and biology · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. The ouroboros of autoimmunity.Nature immunology · 2024
    Review
  10. Review
  11. Review
  12. Infections in the monogenic autoimmune syndrome APECED.Current opinion in immunology · 2021
    Review
  13. Article
  14. Review
  15. Thymus and autoimmunity.Seminars in immunopathology · 2021
    Review
  16. Review
  17. Review
  18. Review
  19. Epidemiology, pathogenesis, and diagnosis of Addison's disease in adults.Journal of endocrinological investigation · 2019
    Review
  20. Article
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 at 6 institutions in 4 countries.

Anette S B WolffDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway; Anette.boe@k2.uib.no.
Jaanika KärnerMolecular Pathology Group, Institute of Biomedicine and Translational Medicine, University of Tartu, 50090 Tartu, Estonia;
Jone F OweDepartment of Clinical Medicine, University of Bergen, 5021 Bergen, Norway; Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway;
Bergithe E V OftedalDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway;
Nils Erik GilhusDepartment of Clinical Medicine, University of Bergen, 5021 Bergen, Norway; Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway;
Martina M ErichsenDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway;
Olle KämpeDepartment of Medicine, Solna, Karolinska University Hospital, Karolinska Institutet, SE-171 76 Stockholm, Sweden;
Anthony MeagerBiotherapeutics Group, The National Institute for Biological Standards and Control, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom; and.
Pärt PetersonMolecular Pathology Group, Institute of Biomedicine and Translational Medicine, University of Tartu, 50090 Tartu, Estonia;
Kai KisandMolecular Pathology Group, Institute of Biomedicine and Translational Medicine, University of Tartu, 50090 Tartu, Estonia;
Nick WillcoxDepartment of Clinical Neurology, Weatherall Institute for Molecular Medicine, University of Oxford, Oxford OX3 9DU, United Kingdom.
Eystein S HusebyeDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway; Department of Medicine, Haukeland University Hospital, 5021 Bergen, Norway;
Haukeland University Hospital · NOUniversity of Bergen · NOUniversity of Tartu · EEKarolinska Institutet · SENational Institute for Biological Standards and Control · GBUniversity of Oxford · GB

Funding

Medical Research Council G7811883
6 · The paper itself

Abstract

Patients with the autoimmune polyendocrine syndrome type I (APS-I), caused by mutations in the autoimmune regulator (AIRE) gene, and myasthenia gravis (MG) with thymoma, show intriguing but unexplained parallels. They include uncommon manifestations like autoimmune adrenal insufficiency (AI), hypoparathyroidism, and chronic mucocutaneous candidiasis plus autoantibodies neutralizing IL-17, IL-22, and type I IFNs. Thymopoiesis in the absence of AIRE is implicated in both syndromes. To test whether these parallels extend further, we screened 247 patients with MG, thymoma, or both for clinical features and organ-specific autoantibodies characteristic of APS-I patients, and we assayed 26 thymoma samples for transcripts for AIRE and 16 peripheral tissue-specific autoantigens (TSAgs) by quantitative PCR. We found APS-I-typical autoantibodies and clinical manifestations, including chronic mucocutaneous candidiasis, AI, and asplenia, respectively, in 49 of 121 (40%) and 10 of 121 (8%) thymoma patients, but clinical features seldom occurred together with the corresponding autoantibodies. Both were rare in other MG subgroups (n = 126). In 38 patients with APS-I, by contrast, we observed neither autoantibodies against muscle Ags nor any neuromuscular disorders. Whereas relative transcript levels for AIRE and 7 of 16 TSAgs showed the expected underexpression in thymomas, levels were increased for four of the five TSAgs most frequently targeted by these patients' autoantibodies. Therefore, the clinical and serologic parallels to APS-I in patients with thymomas are not explained purely by deficient TSAg transcription in these aberrant AIRE-deficient tumors. We therefore propose additional explanations for the unusual autoimmune biases they provoke. Thymoma patients should be monitored for potentially life-threatening APS-I manifestations such as AI and hypoparathyroidism.

Indexed as

Adrenal InsufficiencyAdultAIRE ProteinAutoantibodiesAutoantigensCandidiasis, Chronic MucocutaneousFemaleHeterotaxy SyndromeHumansHypoparathyroidismInterferon Type IInterleukin-17Interleukin-22InterleukinsMaleMiddle AgedAIRE ProteinAutoantibodiesAutoantigensInterferon Type IInterleukin-17Interleukin-22InterleukinsTranscription Factors

Identifiers

PMID25230752
PMCPMC4190667
OpenAlexW1852479680

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.