Evidence map›Paper›PMID 34911754›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen.

Nils Landegren, Norito Ishii, Maribel Aranda-Guillén, Hörður Ingi Gunnarsson, Fabian Sardh, Åsa Hallgren, Mona Ståhle, Eva Hagforsen, Maria Bradley, Per-Henrik D Edqvist and 12 more

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Transglutaminase 1: Emerging Functions beyond Skin.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. 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

22 authors at 7 institutions in 5 countries.

Nils LandegrenDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala 751 23, Sweden; nils.landegren@imbim.uu.se.ORCID 0000-0002-6163-9540
Norito IshiiDepartment of Dermatology, Kurume University School of Medicine, Kurume 830-0111, Japan.ORCID 0000-0002-1199-6611
Maribel Aranda-GuillénCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.ORCID 0000-0003-0050-704X
Hörður Ingi GunnarssonCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.
Fabian SardhCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.
Åsa HallgrenCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.
Mona StåhleDermatology Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Stockholm 171 76, Sweden.ORCID 0000-0002-3916-9343
Eva HagforsenDepartment of Medical Sciences, Uppsala University 751 85, Sweden.
Maria BradleyDermatology Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Stockholm 171 76, Sweden.ORCID 0000-0001-7192-5041
Per-Henrik D EdqvistDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.ORCID 0000-0002-8330-0134
Fredrik PonténDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.ORCID 0000-0003-0703-3940
Outi MäkitieChildren's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki 00014, Finland.ORCID 0000-0002-4547-001X
Liv EidsmoDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Stockholm 171 76, Sweden.
Lars NorlénDepartment of Cell and Molecular Biology, Karolinska Institute, Solna 171 77, Sweden.
Adnane AchourScience for Life Laboratory, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.ORCID 0000-0003-0432-710X
Ingrid DahlbomDepartment of Women's Health, Uppsala University, Uppsala 751 85, Sweden.ORCID 0000-0002-0560-9275
Ilma Korponay-SzabóHeim Pál National Paediatric Institute, Coeliac Disease Centre, Budapest 1089, Hungary.ORCID 0000-0003-0554-2629
Daniel AgardhThe Diabetes and Celiac Disease Unit, Department of Clinical Sciences, Lund University, Lund 221 00, Sweden.ORCID 0000-0003-1435-1234
Mohammad AlimohammadiDepartment of Medical Sciences, Uppsala University 751 85, Sweden.ORCID 0000-0001-5937-1963
Daniel ErikssonCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.ORCID 0000-0001-5473-3312
Takashi HashimotoDepartment of Dermatology, Osaka City University Graduate School of Medicine, Osaka 545-8585, Japan.ORCID 0000-0002-0144-3255
Olle KämpeCenter for Molecular Medicine, Department of Medicine (Solna), Karolinska Institutet, Stockholm 171 76, Sweden.ORCID 0000-0001-6091-9914
Karolinska University Hospital · SEUppsala University · SEKarolinska Institutet · SEKurume University · JPLund University · SEOsaka City University · JPUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoantigen discovery is a critical challenge for the understanding and diagnosis of autoimmune diseases. While autoantibody markers in current clinical use have been identified through studies focused on individual disorders, we postulated that a reverse approach starting with a putative autoantigen to explore multiple disorders might hold promise. We here targeted the epidermal protein transglutaminase 1 (TGM1) as a member of a protein family prone to autoimmune attack. By screening sera from patients with various acquired skin disorders, we identified seropositive subjects with the blistering mucocutaneous disease paraneoplastic pemphigus. Validation in further subjects confirmed TGM1 autoantibodies as a 55% sensitive and 100% specific marker for paraneoplastic pemphigus. This gene-centric approach leverages the wealth of data available for human genes and may prove generally applicable for biomarker discovery in autoimmune diseases.

Indexed as

AdolescentAdultAgedAged, 80 and overAutoantigensBiomarkersCase-Control StudiesChildFemaleHumansMaleMiddle AgedParaneoplastic SyndromesPemphigusTransglutaminasesYoung AdultAutoantigensBiomarkerstransglutaminase 1Transglutaminasesautoantibodiesautoimmunitybiomarkersparaneoplastictransglutaminase

Identifiers

PMID34911754
PMCPMC8713791
OpenAlexW4200602953

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.