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Induction of Alloantigen-specific Anergy in Human Peripheral Blood Mononuclear Cells by Alloantigen Stimulation with Co-stimulatory Signal Blockade
Published on: March 14, 2011
cis-urocanic acid failed to affect in vitro human Langerhans cell allostimulatory function
F M Rattis1, J Péguet-Navarro, P Courtellemont
1Laboratoire Peau Humaine et Immunité, INSERM U346, Hôpital E. Herriot, Lyon, France.
This study found that cis-urocanic acid (UCA) does not directly impact human Langerhans cell (LC) antigen-presenting function, even after UV exposure. Cis-UCA does not alter LC allostimulatory capacity or potentiate UV-induced immunosuppression.
Area of Science:
- Immunodermatology
- Photobiology
- Cellular Immunology
Background:
- Urocanic acid (UCA) is a major skin component absorbing UVB radiation.
- Trans-UCA converts to cis-UCA upon UVB exposure.
- Langerhans cells (LCs) are key antigen-presenting cells in the skin.
Purpose of the Study:
- To investigate the effect of purified cis-UCA on human LC allostimulatory function.
- To determine if cis-UCA modulates T-cell responses influenced by UVB-irradiated LCs.
Main Methods:
- Mixed epidermal cell-lymphocyte reaction (MELR) assay.
- Use of enriched LC (eLC) and purified LC (pLC) suspensions.
- Incubation of LCs with varying concentrations of cis-UCA and trans-UCA.
- Assessment of T-cell proliferation following UVB exposure of LCs.
Main Results:
- cis-UCA and trans-UCA did not alter the T-cell response mediated by untreated eLC or pLC.
- UVB irradiation of eLC and pLC significantly inhibited their allostimulatory capacity.
- cis-UCA did not potentiate UVB-induced immunosuppression in LCs.
- Preincubation of LCs with cis-UCA did not affect their subsequent antigen-presenting function.
Conclusions:
- cis-UCA exhibits no direct influence on the antigen-presenting function of human Langerhans cells.
- The study suggests cis-UCA does not play a role in modulating LC-mediated immune responses in the context of UVB exposure.
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