Evidence map›Paper›PMID 24935676›Full record

ArticlePigment cell & melanoma research2014

Immune responses in a mouse model of vitiligo with spontaneous epidermal de- and repigmentation.

Jonathan M Eby, Hee-Kap Kang, Jared Klarquist, Shilpak Chatterjee, Jeffrey A Mosenson, Michael I Nishimura, Elizabeth Garrett-Mayer, B Jack Longley, Victor H Engelhard, Shikhar Mehrotra and 1 more

Abstract read
In one paragraph

Article in Pigment cell & melanoma research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The immunology of vitiligo.Nature reviews. Immunology · 2026
    Review
  3. Article
  4. Deciphering Depigmentation: Mouse Models for Vitiligo Research.The Journal of investigative dermatology · 2025
    Review
  5. Article
  6. The role of regulatory T cells in vitiligo and therapeutic advances: a mini-review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. The role of IL-17 in vitiligo: A review.Autoimmunity reviews · 2016
    Review
  12. 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

11 authors.

Jonathan M EbyOncology Research Institute, Loyola University Chicago, Chicago, IL, USA.
Hee-Kap Kang
Jared Klarquist
Shilpak Chatterjee
Jeffrey A Mosenson
Michael I Nishimura
Elizabeth Garrett-Mayer
B Jack Longley
Victor H Engelhard
Shikhar Mehrotra
I Caroline Le Poole

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
Autoimmune vitiligo and tolerance in the immune response to a melanoma antigenR01AI068836 · NIAID · UNIVERSITY OF VIRGINIA · PI ENGELHARD, VICTOR H · 2007 to 2011
$2.1M
Modulating tolerance in a spontaneous mouse model of autoimmune vitiligoR01AR057643 · NIAMS · LOYOLA UNIVERSITY CHICAGO · PI LE POOLE, I. CAROLINE · 2010 to 2014
$1.6M
Development & Characterization of Tyrosinase Epitope Specific TCR Transgenic MiceR21AR056524 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHROTRA, SHIKHAR · 2009 to 2010
$363k
NCI NIH HHS P01 CA154778NCI NIH HHS P01CA154778NIAID NIH HHS AI068836NIAID NIH HHS R01 AI068836NIAMS NIH HHS AR057643-03NIAMS NIH HHS R01 AR057643NIAMS NIH HHS R21 AR056524
6 · The paper itself

Abstract

To generate a mouse model of spontaneous epidermal depigmentation, parental h3TA2 mice, expressing both a human-derived, tyrosinase-reactive T-cell receptor on T cells and the matching HLA-A2 transgene, were crossed to keratin 14-promoter driven, stem cell factor transgenic (K14-SCF) mice with intra-epidermal melanocytes. In resulting Vitesse mice, spontaneous skin depigmentation precedes symmetrical and sharply demarcated patches of graying hair. Whereas the SCF transgene alone dictates a greater retinoic acid receptor-related orphan receptor gamma (RORγt)(+) T-cell compartment, these cells displayed markedly increased IL-17 expression within Vitesse mice. Similar to patient skin, regulatory T cells were less abundant compared with K14-SCF mice, with the exception of gradually appearing patches of repigmenting skin. The subtle repigmentation observed likely reflects resilient melanocytes that coexist with skin-infiltrating, melanocyte-reactive T cells. Similar repigmenting lesions were found in a different TCR transgenic model of vitiligo developed on an SCF transgenic background, supporting a role for SCF in repigmentation.

Indexed as

ImmunityPigmentationAnimalsCell LineDisease Models, AnimalEpidermisEpitopesHumansHypopigmentationInterleukin-17Mice, Inbred C57BLMice, TransgenicMonophenol MonooxygenaseReceptors, Antigen, T-CellStem Cell FactorT-Lymphocytes, RegulatoryEpitopesInterleukin-17Monophenol MonooxygenaseReceptors, Antigen, T-CellStem Cell FactorIL-17mouse modelpigmentationstem cell factorT-cell receptorvitiligo

Identifiers

PMID24935676
PMCPMC4470702

What OpenQuestion holds

Textmetadata
LicenceTDM
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.