Dissecting the complexity of γδ T-cell subsets in skin homeostasis, inflammation, and malignancy
- PMID: 33259837
- DOI: 10.1016/j.jaci.2020.11.023
Dissecting the complexity of γδ T-cell subsets in skin homeostasis, inflammation, and malignancy
Abstract
γδ T cells are much less common than αβ T cells, accounting for 0.5% to 5% of all T lymphocytes in the peripheral blood and lymphoid tissues in mice and humans. However, they are the most abundant T-lymphocyte subset in some epithelial barriers such as mouse skin. γδ T cells are considered innate lymphocytes because of their non-MHC restricted antigen recognition, as well as because of their rapid response to cytokines, invading pathogens, and malignant cells. Exacerbated expansion and activation of γδ T cells in the skin is a common feature of acute and chronic skin inflammation such as psoriasis and contact or atopic dermatitis. Different γδ T-cell subsets showing differential developmental and functional features are found in mouse and human skin. This review discusses the state of the art of research and future perspectives about the role of the different subsets of γδ T-cells detected in the skin in steady-state, psoriasis, dermatitis, infection, and malignant skin diseases. Also, we highlight the differences between human and mouse γδ T cells in skin homeostasis and inflammation, as understanding the differential role of each subtype of skin γδ T cells will improve the discovery of new therapies.
Keywords: atopic dermatitis; cancer; infection; psoriasis; skin; γδ T cells.
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.
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