Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Feb;77(2):513-524.
doi: 10.1111/all.14986. Epub 2021 Jul 21.

CD8+ tissue-resident memory T cells recruit neutrophils that are essential for flare-ups in contact dermatitis

Affiliations

CD8+ tissue-resident memory T cells recruit neutrophils that are essential for flare-ups in contact dermatitis

Anders B Funch et al. Allergy. 2022 Feb.

Abstract

Background: Allergic contact dermatitis (ACD) is classically described as a delayed-type hypersensitivity reaction. However, patients often experience flare-ups characterized by itching erythema, edema, and often vesicles occurring within hours after re-exposure of previously sensitized skin to the specific contact allergen. Recent studies have indicated that skin-resident memory T (TRM ) cells play a central role in ACD. However, the pathogenic role of TRM cells in allergen-induced flare-ups is not known.

Methods: By the use of various mouse models and cell depletion protocols, we investigated the role of epidermal TRM cells in flare-up reactions to the experimental contact allergen 1-fluoro-2,4-dinitrobenzene. The inflammatory response was measured by changes in ear thickness, and the cellular composition in epidermis was determined by flow cytometry and confocal microscopy. Finally, adaptive transfer and inhibitors were used to determine the role of TRM cells, neutrophils, and CXCL1/CXCL2 in the response.

Results: We show that CD8+ TRM cells initiate massive infiltration of neutrophils in the epidermis within 12 h after re-exposure to the contact allergen. Depletion of neutrophils before re-exposure to the allergen abrogated the flare-up reactions. Furthermore, we demonstrate that CD8+ TRM cells mediate neutrophil recruitment by inducing CXCL1 and CXCL2 production in the skin, and that blockage of the C-X-C chemokine receptor type 1 and 2 inhibits flare-up reactions and neutrophil infiltration.

Conclusion: As the first, we show that epidermal CD8+ TRM cells cause ACD flare-ups by rapid recruitment of neutrophils to the epidermis.

Keywords: CXCL1; CXCL2; allergic contact dermatitis; epidermal-resident T cells; neutrophils.

PubMed Disclaimer

References

REFERENCES

    1. Diepgen TL, Ofenloch RF, Bruze M, et al. Prevalence of contact allergy in the general population in different European regions. Br J Dermatol. 2016;174:319-329.
    1. Kaplan DH, Igyártó BZ, Gaspari AA. Early immune events in the induction of allergic contact dermatitis. Nat Rev Immunol. 2012;12:114-124.
    1. Ahlström MG, Menné T, Thyssen JP, Johansen JD. Nickel allergy in a Danish population 25 years after the first nickel regulation. Contact Dermatitis. 2017;76:325-332.
    1. Gaide O, Emerson RO, Jiang X, et al. Common clonal origin of central and resident memory T cells following skin immunization. Nat Med. 2015;21:647-653.
    1. Schmidt JD, Ahlstrøm MG, Johansen JD, et al. Rapid allergen-induced interleukin-17 and interferon-gamma secretion by skin-resident memory CD8+ T cells. Contact Dermatitis. 2016;76:218-227.

Publication types

LinkOut - more resources