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A role for human skin–resident T cells in wound healing

Epidermal T cells have been shown to play unique roles in tissue homeostasis and repair in mice through local secretion of distinct growth factors in the skin. Human epidermis contains both αβ(+) and γδ(+) T cells whose functional capabilities are not understood. We demonstrate that human epidermal...

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Detalles Bibliográficos
Autores principales: Toulon, Antoine, Breton, Lionel, Taylor, Kristen R., Tenenhaus, Mayer, Bhavsar, Dhaval, Lanigan, Caroline, Rudolph, Ross, Jameson, Julie, Havran, Wendy L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715110/
https://www.ncbi.nlm.nih.gov/pubmed/19307328
http://dx.doi.org/10.1084/jem.20081787
Descripción
Sumario:Epidermal T cells have been shown to play unique roles in tissue homeostasis and repair in mice through local secretion of distinct growth factors in the skin. Human epidermis contains both αβ(+) and γδ(+) T cells whose functional capabilities are not understood. We demonstrate that human epidermal T cells are able to produce insulin-like growth factor 1 (IGF-1) upon activation and promote wound healing in a skin organ culture model. Moreover, an analysis of the functional capabilities of T cells isolated from acute versus chronic wounds revealed a striking difference. Both αβ(+) and Vδ1(+) T cells isolated from acute wounds actively produced IGF-1, demonstrating that they are activated during tissue damage to participate in wound repair. In contrast, IGF-1 production could not be detected in T cells isolated from chronic wounds. In fact, skin T cells isolated from chronic wounds were refractory to further stimulation, suggesting an unresponsive state. Collectively, these results define a novel role for human epidermis–resident T cells in wound healing and provide new insight into our understanding of chronic wound persistence.