Evidence map›Paper›PMID 20844203›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Langerhans cells serve as immunoregulatory cells by activating NKT cells.

Atsushi Fukunaga, Noor M Khaskhely, Ying Ma, Coimbatore S Sreevidya, Kumiko Taguchi, Chikako Nishigori, Stephen E Ullrich

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 77 citations in OpenAlex.

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  12. DNA Damage Response and Immune Defense.International journal of molecular sciences · 2020
    Review
  13. Lipids in ultraviolet radiation-induced immune modulation.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2020
    Review
  14. Review
  15. Review
  16. Langerhans Cells Facilitate UVB-Induced Epidermal Carcinogenesis.The Journal of investigative dermatology · 2015
    Article
  17. Review
  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

7 authors at 3 institutions in 2 countries.

Atsushi FukunagaDepartment of Immunology, Center for Cancer Immunology Research, University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA.
Noor M Khaskhely
Ying Ma
Coimbatore S Sreevidya
Kumiko Taguchi
Chikako Nishigori
Stephen E Ullrich
The University of Texas MD Anderson Cancer Center · USKobe University · JPUniversity of Houston · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
Does UV-induced Unconventional Mast Cell Migration Activate Immune Suppression?R01CA131207 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ULLRICH, STEPHEN E · 2008 to 2012
$1.6M
Inflammatory mediators and UV-induced carcinogenesisR01CA112660 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ULLRICH, STEPHEN E · 2005 to 2009
$1.1M
ARE UV INDUCED TUMOR SUPPRESSOR CELLS TH2 CELLS?R01ES007327 · NIEHS · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI ULLRICH, STEPHEN E · 1996 to 1998
–
NCI NIH HHS CA112660NCI NIH HHS CA131207NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA112660NCI NIH HHS R01 CA131207
6 · The paper itself

Abstract

Ultraviolet exposure alters the morphology and function of epidermal Langerhans cells (LCs), which play a role in UV-induced immune suppression. It is generally believed that UV exposure triggers the migration of immature LCs from the skin to the draining lymph nodes (LNs), where they induce tolerance. However, because most of the previous studies employed in vitro UV-irradiated LCs, the data generated may not adequately reflect what is happening in vivo. In this study, we isolated migrating LCs from the LNs of UV-irradiated mice and studied their function. We found prolonged LC survival in the LNs of UV-irradiated mice. LCs were necessary for UV-induced immune suppression because no immune suppression was observed in LC-deficient mice. Transferring LCs from UV-irradiated mice into normal recipient animals transferred immune suppression and induced tolerance. We found that LCs colocalized with LN NKT cells. No immune suppression was observed when LCs were transferred from UV-irradiated mice into NKT cell-deficient mice. NKT cells isolated from the LNs of UV-irradiated mice secreted significantly more IL-4 than NKT cells isolated from nonirradiated controls. Injecting the wild-type mice with anti-IL-4 blocked the induction of immune suppression. Our findings indicate that UV exposure activates the migration of mature LC to the skin draining LNs, where they induce immune regulation in vivo by activating NKT cells.

Indexed as

AnimalsChemotaxis, LeukocyteFluorescent Antibody TechniqueImmune ToleranceLangerhans CellsLymphocyte ActivationMiceNatural Killer T-CellsUltraviolet Rays

Identifiers

PMID20844203
PMCPMC2950871
OpenAlexW2166860753

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.