Evidence map›Paper›PMID 35245125›Full record

ArticleScience advances2022

Abrogation of self-tolerance by misfolded self-antigens complexed with MHC class II molecules.

Hui Jin, Kazuki Kishida, Noriko Arase, Sumiko Matsuoka, Wataru Nakai, Masako Kohyama, Tadahiro Suenaga, Ken Yamamoto, Takehiko Sasazuki, Hisashi Arase

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Observational
  7. Neoself Antigens Presented on MHC Class II Molecules in Autoimmune Diseases.Advances in experimental medicine and biology · 2024
    Article
  8. Anti-β2-glycoprotein I/HLA-DR Antibody and Adverse Obstetric Outcomes.International journal of molecular sciences · 2023
    Article
  9. A novel vaccine targeting β1-adrenergic receptor.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
    Article
  10. Review
  11. 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

10 authors at 5 institutions in 1 country.

Hui JinLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.ORCID 0000-0001-8096-2565
Kazuki KishidaLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.
Noriko AraseDepartment of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Suita City, Osaka 565-0871, Japan.ORCID 0000-0003-3966-3437
Sumiko MatsuokaDepartment of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Suita City, Osaka 565-0871, Japan.
Wataru NakaiLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.ORCID 0000-0001-7350-3125
Masako KohyamaLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.
Tadahiro SuenagaLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.
Ken YamamotoDepartment of Medical Biochemistry, Kurume University School of Medicine, Kurume City, Fukuoka 830-0011, Japan.
Takehiko SasazukiKyushu University Institute for Advanced Study, Fukuoka City, Fukuoka 812-8582, Japan.ORCID 0000-0003-2530-4257
Hisashi AraseLaboratory of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Suita City, Osaka 565-0871, Japan.ORCID 0000-0002-1153-3166
Osaka City University · JPFukushima Medical University · JPKurume University Medical Center · JPKyushu University · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Specific MHC class II alleles are strongly associated with susceptibility to various autoimmune diseases. Although the primary function of MHC class II molecules is to present peptides to helper T cells, MHC class II molecules also function like a chaperone to transport misfolded intracellular proteins to the cell surface. In this study, we found that autoantibodies in patients with Graves' disease preferentially recognize thyroid-stimulating hormone receptor (TSHR) complexed with MHC class II molecules of Graves' disease risk alleles, suggesting that the aberrant TSHR transported by MHC class II molecules is the target of autoantibodies produced in Graves' disease. Mice injected with cells expressing mouse TSHR complexed with MHC class II molecules, but not TSHR alone, produced anti-TSHR autoantibodies. These findings suggested that aberrant self-antigens transported by MHC class II molecules exhibit antigenic properties that differ from normal self-antigens and abrogate self-tolerance, providing a novel mechanism for autoimmunity.

Identifiers

PMID35245125
PMCPMC8896794
OpenAlexW4221001658

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.