Cited by 88Skin Protection and AgingImmunotherapy and Immune ResponsesT-cell and B-cell Immunology

Epidermal langerhans cell depletion after artificial ultraviolet B irradiation of human skin in vivo: Apoptosis versus migration

Open access
Kölgen, Wendy, Both, Hilde, van Weelden, Huib, Guikers, Kees L.H., Bruijnzeel-Koomen, Carla A.F.M., Knol, Edward F., van Vloten, Willem A., de Gruijl, Frank R.·2002·Journal of Investigative Dermatology

Abstract

Ultraviolet B radiation can suppress cellular immunity. One of the mechanisms related to this immunosuppression is the disappearance of Langerhans cells from the epidermis. The aim of this study was to establish the mechanism of ultraviolet B-induced Langerhans cell disappearance in healthy individuals. The two most likely mechanisms for Langerhans cell disappearance are apoptosis and migration. Apoptosis was assessed in vivo by exposing buttock skin of 10 healthy volunteers to six minimal erythema doses of ultraviolet B. Only very few apoptotic Langerhans cells could be observed in sections from the ultraviolet B-exposed skin. Migration of Langerhans cells cannot be established in skin sections and suction blisters were therefore raised in an attempt to trap migrating Langerhans cells in the sub-basal membrane blister fluid. Blisters were raised on the flexor side of the lower arm of 30 healthy volunteers at several time points after exposure of the skin to six minimal erythema doses of ultraviolet B. Blister fluid was collected and blister roofs were removed to check for Langerhans cell disappearance. Langerhans cells were detected in the blister fluid of the ultraviolet B-exposed skin and not of the unexposed skin. The number of Langerhans cells in the blister fluid peaked at about 18 h after ultraviolet exposure, which coincided with the largest depletion of Langerhans cells in the blister roof. A fraction (20-30%) of the Langerhans cells in the blister fluid stained positive for DNA damage (cyclobutyl pyrimidine dimers), showing that they originated from the epidermis. Ultraviolet B-induced Langerhans cell disappearance appears to be mainly attributable to migration.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1046/j.1523-1747.2002.01742.x

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • UV can deplete Langerhans cells in the epidermis and impair their migratory capacity, leading to their accumulation in the dermis.

    “Furthermore, UV can deplete LCs in the epidermis and impair their migratory capacity, leading to their accumulation in the dermis.”

    From Molecular Mechanisms of UV-Induced Apoptosis and Its Effects on Skin Residential Cells: The Implication in UV-Based Phototherapy (2013) · cites this paper as [62]

    The Results and Discussion (pp. 812–817) support epidermal Langerhans cell depletion after UVB exposure and identify migration as its main cause. They do not show that UV impairs the cells’ migratory capacity or causes them to accumulate in the dermis; the study instead detected migrating cells in blister fluid. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • UVR can induce the depletion of Langerhans cells in the epidermis and impair the migratory capacity of Langerhans cells, leading to their accumulation in the dermis.

    “UVR can induce the depletion of LCs in the epidermis and impair the migratory capacity of LCs, leading to their accumulation in the dermis [62].”

    From Molecular Mechanisms of UV-Induced Apoptosis and Its Effects on Skin Residential Cells: The Implication in UV-Based Phototherapy (2013) · cites this paper as [62]

    The Results report epidermal Langerhans-cell depletion after UVB exposure, and the Discussion concludes that the depletion is mainly caused by migration. The paper does not establish that UVB impairs their migratory capacity or causes them to accumulate in the dermis; it detects migrating cells in blister fluid instead. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cited by

Sorted by citations

Authors
Kölgen, W., Both, H., van Weelden, H., Guikers, K. L. H., Bruijnzeel-Koomen, C. A. F. M., Knol, E. F., van Vloten, W. A., & de Gruijl, F. R.
Affiliations
University Medical Center Utrecht (NL)
Corresponding author
Kölgen, Wendy
Venue
Journal of Investigative Dermatology
Publisher
Elsevier BV
Published
2002-05
Volume
118
Issue
5
Pages
812-817
ISSN
0022-202X (ISSN-L)
OpenAlex
W2082775445
Cited by
88
References
0
Citations by year
2026: 3 · 2025: 1 · 2024: 3 · 2023: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 3 · 2017: 2 · 2016: 3 · 2015: 2 · 2014: 7 · 2013: 6 · 2012: 6
FWCI
5.80
Type
journal article
Language
en
Open access
Locations
  • Journal of Investigative Dermatology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Dermatology › Skin Protection and Aging
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
Langerhans cells, UV-B radiation, immunosuppression, apoptosis, cell migration, epidermis, suction blister, blister fluid, DNA damage, minimal erythema dose, skin
MeSH terms
Adult, Blister, Cell Movement, DNA Damage, Epidermis, Female, Humans, Langerhans Cells, Male, Middle Aged, Pyrimidine Dimers, Suction, Ultraviolet Rays, Apoptosis, Antigens, CD1, Caspases, In Situ Nick-End Labeling, Caspase 3

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review