UV radiation recruits CD4+GATA3+ and CD8+GATA3+ Tcells while altering the lipid microenvironment following inflammatory resolution in human skin in vivo

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives:
Solar ultraviolet radiation (UVR) has major adverse effects on human health. While the mechanisms responsible for induction of UVR-induced inflammation are well-documented, the mediation of its resolution and longer-term adaptive-homeostasis is unknown. Therefore, we examined the skin immune and lipid profile over time following UVR-inflammation.

Methods:
To investigate the self-resolving events of UVR inflammation in vivo, human skin was exposed to a single pro-inflammatory dose of UVR. Skin biopsies and suction blister fluid were taken at intervals up to 2 weeks post-UVR. The immune infiltrate was quantified by immunohistochemisty and lipid mediators were profiled by liquid chromatography/mass spectrometry.

Results:
We identified that cellular resolution events including switching of macrophage phenotype apply to human sunburn. However, UVR-induced inflammation in humans involves a post resolution phase that differs from other experimental models. We demonstrate that 2 weeks after the initiating UVR stimulus there is considerable immune activity with CD8+GATA3+ T40 cells maintained in human skin. Our results challenge the dogma of CD4+FOXP3+ T-cells being the main effector CD4+ T-cell population following UVR, with CD4+GATA3+ T-cells the
dominant phenotype. Furthermore, lipid mediators are elevated 14 days post-UVR, demonstrating the skin lipid-microenvironment does not revert to the tissue setting occurring prior to UVR exposure.

Conclusion:
We have identified for the first time that CD4+GATA3+ and CD8+GATA3+ T-cell
subpopulations are recruited to UVR-inflamed human skin, demonstrating discrepancies between the adaptive-UVR response in mice and humans. Future strategies to abrogate UVR effects may target these T-cell subpopulations and also the persistent alteration of the lipid microenvironment post-UVR.

Bibliographical metadata

Original languageEnglish
Article numbere01104
JournalClinical & translational immunology
Volume9
Issue number4
Publication statusPublished - 2 Apr 2020

Related information

Researchers

View all