Evidence map›Paper›PMID 30131581›Full record

ArticleScientific reports2018

Induction of alopecia areata in C3H/HeJ mice using polyinosinic-polycytidylic acid (poly[I:C]) and interferon-gamma.

Jung-Min Shin, Dae-Kyoung Choi, Kyung-Cheol Sohn, Jung-Woo Koh, Young Ho Lee, Young-Joon Seo, Chang Deok Kim, Jeung-Hoon Lee, Young Lee

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. The Involvement of RIPK1 in Alopecia Areata.International journal of molecular sciences · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Alopecia Areata: Burden of Disease, Approach to Treatment, and Current Unmet Needs.Clinical, cosmetic and investigational dermatology · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Molecular medicine reports · 2022
    Article
  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

9 authors at 2 institutions in 1 country.

Jung-Min ShinDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Dae-Kyoung ChoiBiomedical Research Institute, Chungnam National University Hospital, Daejeon, Korea.
Kyung-Cheol SohnDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Jung-Woo KohDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Young Ho LeeDepartment of Anatomy, School of Medicine, Chungnam National University, Daejeon, Korea.
Young-Joon SeoDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Chang Deok KimDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.ORCID 0000-0001-9341-6491
Jeung-Hoon LeeDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Young LeeDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea. resina20@cnu.ac.kr.ORCID 0000-0001-9205-1785
Chungnam National University · KRChungnam National University Hospital · KR

Funding

National Research Foundation of Korea (NRF) 2015R1A2A2A01004664
6 · The paper itself

Abstract

Alopecia areata (AA) is a chronic, relapsing hair-loss disorder that is considered to be a T-cell-mediated autoimmune disease. Several animal models for AA have been created to investigate the pathophysiology and screen for effective therapeutic targets. As C3H/HeJ mice develop AA spontaneously in a low frequency, a novel animal model is needed to establish an AA-like condition faster and more conveniently. In this study, we present a novel non-invasive AA rodent model that avoids skin or lymph-node cell transfer. We simply injected C3H/HeJ mice subcutaneously with interferon-gamma (IFNγ) along with polyinosinic:polycytidylic acid (poly[I:C]), a synthetic dsRNA, to initiate innate immunity via inflammasome activation. Approximately 80% of the IFNγ and poly(I:C) co-injected mice showed patchy AA lesions after 8 weeks. None of the mice displayed hair loss in the IFNγ or poly(I:C) solely injection group. Immunohistochemical staining of the AA lesions revealed increased infiltration of CD4

Indexed as

Disease Models, AnimalAlopecia AreataAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedChemokines, CXCDrug SynergismFemaleHumansInjections, SubcutaneousInterferon-gammaInterleukin-1betaMiceMice, Inbred C3HNLR Family, Pyrin Domain-Containing 3 ProteinChemokines, CXCIL1B protein, mouseInterferon-gammaInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePoly I-C

Identifiers

PMID30131581
PMCPMC6104095
OpenAlexW2887555485

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.