Evidence map›Paper›PMID 16920575›Full record

ReviewAutoimmunity reviews2006

Therapeutic implications of autoimmune vitiligo T cells.

Kepa Oyarbide-Valencia, Jasper G van den Boorn, Cecele J Denman, Mingli Li, Jeremy M Carlson, Claudia Hernandez, Michael I Nishimura, Pranab K Das, Rosalie M Luiten, I Caroline Le Poole

Abstract readReview
In one paragraph

Review in Autoimmunity reviews, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

36 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. CCL17-CCR4 axis contributes to the onset of vitiligo in mice.Immunity, inflammation and disease · 2021
    Article
  8. Tumor rejection properties of gp100Molecular immunology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

10 authors at 3 institutions in 2 countries.

Kepa Oyarbide-ValenciaDepartment of Pathology/Oncology Institute, Loyola University Chicago, 2160 South First Ave, Bldg 112, Rm 203, Maywood, IL 60153, USA.
Jasper G van den Boorn
Cecele J Denman
Mingli Li
Jeremy M Carlson
Claudia Hernandez
Michael I Nishimura
Pranab K Das
Rosalie M Luiten
I Caroline Le Poole
Loyola University Chicago · USUniversity of Amsterdam · NLUniversity of Illinois Chicago · US

Funding

Function and Regulation of MDMXR01CA109636 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI CHEN, JIANDONG · 2004 to 2014
$2.8M
Tumor Recognition by TCR Transduced CD4+ and CD8+T CellsR01CA090873 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2001 to 2004
$1.3M
Autoimmune vitiligo as a roadmap to melanoma therapyR01CA109536 · NCI · LOYOLA UNIVERSITY CHICAGO · PI LE POOLE, ISABELLE CAROLINE · 2005 to 2007
$686k
Stress proteins in autoimmune depigmentationR03AR050137 · NIAMS · LOYOLA UNIVERSITY CHICAGO · PI LE POOLE, ISABELLE CAROLINE · 2003 to 2005
$222k
NCI NIH HHS CA90873NCI NIH HHS R01 CA090873NCI NIH HHS R01 CA109536NCI NIH HHS R01 CA109636NIAMS NIH HHS R03 AR050137NIAMS NIH HHS R03 AR50137
6 · The paper itself

Abstract

Vitiligo is an autoimmune disease presenting with progressive loss of skin pigmentation. The disease strikes 1% of the world population, generally during teenage years. The progressive loss of melanocytes from depigmenting vitiligo skin is accompanied by cellular infiltrates containing both CD4+ and CD8+ T lymphocytes. Infiltrating cytotoxic T cells with high affinity T cell receptors have likely escaped clonal deletion in the thymus, allowing such T cells to enter the circulation. Through the expression of CLA, these T cells home to the skin where they express type 1-cytokine profiles and mediate melanocyte apoptosis via the granzyme/perforin pathway. T cells found juxtapositionally apposed to remaining melanocytes can be isolated from the skin. Vitiligo T cells have demonstrated reactivity to antigens previously recognized as target antigens for T cells infiltrating melanoma tumors. In a comparison to existing melanoma-derived T cells, vitiligo T cells displayed superior reactivity towards melanoma cells. It is thought that genes encoding the TCRs expressed by vitiligo skin infiltrating T cells can be cloned and expressed in melanoma T cells, thereby generating a pool of circulating T cells with high affinity for their targets that can re-direct the immune response towards the tumor.

Indexed as

AnimalsHumansMelanomaReceptors, Antigen, T-CellT-LymphocytesVitiligoReceptors, Antigen, T-Cell

Identifiers

PMID16920575
PMCPMC3462656
OpenAlexW2034021163

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.