Evidence map›Paper›PMID 32453712›Full record

ArticleJCI insight2020

A transcriptomic map of murine and human alopecia areata.

Nicholas Borcherding, Sydney B Crotts, Luana S Ortolan, Nicholas Henderson, Nicholas L Bormann, Ali Jabbari

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.1field-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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. TScience advances · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. A virtual memory CD8Nature immunology · 2023
    Article
  12. Functional interrogation of lymphocyte subsets in alopecia areata using single-cell RNA sequencing.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Recent advances in the genetics of alopecia areata.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Applications of Single-Cell Sequencing in Dermatology.Medical science monitor : international medical journal of experimental and clinical research · 2021
    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

6 authors at 3 institutions in 1 country.

Nicholas BorcherdingDepartment of Pathology.
Sydney B CrottsDepartment of Dermatology.
Luana S OrtolanDepartment of Dermatology.
Nicholas HendersonDepartment of Dermatology.
Nicholas L BormannDepartment of Psychiatry, University of Iowa, College of Medicine, Iowa City, Iowa, USA.
Ali JabbariCancer Biology Graduate Program.
Cancer Genetics (United States) · USUniversity of Iowa · USVeterans Health Administration · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Mark E Burkard · 2000 to 2026
$70.0M
Defining T helper cell associated cytokines and mechanisms in Alopecia AreataK08AR069111 · NIAMS · UNIVERSITY OF IOWA · PI JABBARI, ALI · 2016 to 2020
$854k
The role of paracrine WNT5A/RYK in ErbB2-driven tumorigenesisF30CA206255 · NCI · UNIVERSITY OF IOWA · PI BORCHERDING, NICHOLAS · 2017 to 2020
$143k
Determining the role of T cell effector functions in Alopecia AreataI01BX004907 · VA · IOWA CITY VA MEDICAL CENTER · PI JABBARI, ALI · 2020 to 2023
–
BLRD VA I01 BX004907NCI NIH HHS F30 CA206255NCI NIH HHS P30 CA086862NIAMS NIH HHS K08 AR069111
6 · The paper itself

Abstract

Alopecia areata (AA) is a common autoimmune condition, presenting initially with loss of hair without other overt skin changes. The unremarkable appearance of the skin surface contrasts with the complex immune activity occurring at the hair follicle. AA pathogenesis is due to the loss of immune privilege of the hair follicle, leading to autoimmune attack. Although the literature has focused on CD8+ T cells, vital roles for CD4+ T cells and antigen-presenting cells have been suggested. Here, we use single-cell sequencing to reveal distinct expression profiles of immune cells in murine AA. We found clonal expansions of both CD4+ and CD8+ T cells, with shared clonotypes across varied transcriptional states. The murine AA data were used to generate highly predictive models of human AA disease. Finally, single-cell sequencing of T cells in human AA recapitulated the clonotypic findings and the gene expression of the predictive models.

Indexed as

Alopecia AreataAnimalsAutoimmune DiseasesHair FollicleHumansMiceSkinT-LymphocytesTranscriptomeAutoimmunityDendritic cellsImmunologyMacrophagesT cells

Identifiers

PMID32453712
PMCPMC7406251
OpenAlexW3030942425

What OpenQuestion holds

Textmetadata
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.