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Skin CD4(+) memory T cells exhibit combined cluster-mediated retention and equilibration with the circulation

Although memory T cells within barrier tissues can persist as permanent residents, at least some exchange with blood. The extent to which this occurs is unclear. Here we show that memory CD4(+) T cells in mouse skin are in equilibrium with the circulation at steady state. These cells are dispersed t...

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Detalles Bibliográficos
Autores principales: Collins, Nicholas, Jiang, Xiaodong, Zaid, Ali, Macleod, Bethany L., Li, Jane, Park, Chang Ook, Haque, Ashraful, Bedoui, Sammy, Heath, William R., Mueller, Scott N., Kupper, Thomas S., Gebhardt, Thomas, Carbone, Francis R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866325/
https://www.ncbi.nlm.nih.gov/pubmed/27160938
http://dx.doi.org/10.1038/ncomms11514
Descripción
Sumario:Although memory T cells within barrier tissues can persist as permanent residents, at least some exchange with blood. The extent to which this occurs is unclear. Here we show that memory CD4(+) T cells in mouse skin are in equilibrium with the circulation at steady state. These cells are dispersed throughout the inter-follicular regions of the dermis and form clusters with antigen presenting cells around hair follicles. After infection or administration of a contact sensitizing agent, there is a sustained increase in skin CD4(+) T-cell content, which is confined to the clusters, with a concomitant CCL5-dependent increase in CD4(+) T-cell recruitment. Skin CCL5 is derived from CD11b(+) cells and CD8(+) T cells, with the elimination of the latter decreasing CD4(+) T-cell numbers. These results reveal a complex pattern of tissue-retention and equilibration for CD4(+) memory T cells in skin, which is altered by infection and inflammation history.