Evidence map›Paper›PMID 34848535›Full record

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

Peripheral tolerance by Treg via constraining OX40 signal in autoreactive T cells against desmoglein 3, a target antigen in pemphigus.

Hisato Iriki, Hayato Takahashi, Naoko Wada, Hisashi Nomura, Miho Mukai, Aki Kamata, Hiromi Ito, Jun Yamagami, Takeshi Matsui, Yutaka Kurebayashi and 6 more

Open access · hybridAbstract read
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 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Regulatory T cells: From Foxp3 to tolerance-inducing therapies.The Journal of investigative dermatology · 2026
    Review
  3. OX40/OX40L modulation: A target for regulating T cells in cutaneous inflammatory disorders.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Human OX40L-CAR-TScience translational medicine · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Understanding CD4Frontiers in immunology · 2023
    Review
  17. Review
  18. 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

16 authors at 3 institutions in 1 country.

Hisato IrikiDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.ORCID 0000-0003-4022-8950
Hayato TakahashiDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan; amagai@keio.jp hayato_takahashi@keio.jp.ORCID 0000-0001-6768-8821
Naoko WadaDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Hisashi NomuraDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Miho MukaiDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Aki KamataDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Hiromi ItoDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Jun YamagamiDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Takeshi MatsuiLaboratory for Skin Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama City 230-0045, Japan.ORCID 0000-0001-7118-0414
Yutaka KurebayashiDepartment of Pathology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Setsuko Mise-OmataDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Hiroshi NishimasuDepartment of Biological Science, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
Osamu NurekiDepartment of Biological Science, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.ORCID 0000-0003-1813-7008
Akihiko YoshimuraDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Shohei HoriGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
Masayuki AmagaiDepartment of Dermatology, Keio University School of Medicine, Tokyo 160-8582, Japan; amagai@keio.jp hayato_takahashi@keio.jp.ORCID 0000-0003-3314-7052
Keio University · JPThe University of Tokyo · JPTokyo University of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigen-specific peripheral tolerance is crucial to prevent the development of organ-specific autoimmunity. However, its function decoupled from thymic tolerance remains unclear. We used desmoglein 3 (Dsg3), a pemphigus antigen expressed in keratinocytes, to analyze peripheral tolerance under physiological antigen-expression conditions. Dsg3-deficient thymi were transplanted into athymic mice to create a unique condition in which Dsg3 was expressed only in peripheral tissue but not in the thymus. When bone marrow transfer was conducted from high-avidity Dsg3-specific T cell receptor-transgenic mice to thymus-transplanted mice, Dsg3-specific CD4

Indexed as

AbataceptAdoptive TransferAnimalsCoculture TechniquesDesmoglein 3DNA-Binding ProteinsEstrogen AntagonistsFemaleGene Expression RegulationImmune Checkpoint InhibitorsMaleMiceMice, KnockoutPemphigusTamoxifenT-Lymphocytes, RegulatoryAbataceptDesmoglein 3DNA-Binding ProteinsDsg3 protein, mouseEstrogen AntagonistsImmune Checkpoint InhibitorsRag2 protein, mouseTamoxifenautoreactive T cellsFoxp3OX40peripheral immunological toleranceregulatory T cells

Identifiers

PMID34848535
PMCPMC8670434
OpenAlexW3217497643

What OpenQuestion 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 OpenQuestion graph.