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

TitleSkin CD4(+) memory T cells exhibit combined cluster-mediated retention and equilibration with the circulation.
Publication TypeJournal Article
Year of Publication2016
AuthorsCollins, N, Jiang, X, Zaid, A, Macleod, BL, Li, J, Park, COok, Haque, A, Bedoui, S, Heath, WR, Mueller, SN, Kupper, TS, Gebhardt, T, Carbone, FR
JournalNat Commun
Volume7
Pagination11514
Date Published2016 05 10
ISSN2041-1723
KeywordsAdolescent, Adult, Animals, Antigen-Presenting Cells, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Cell Aggregation, Cell Movement, Chemokine CCL5, Female, Hair Follicle, Herpes Simplex, Herpesvirus 1, Human, Humans, Immunologic Memory, Interferon-gamma, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Middle Aged, Skin, Young Adult
Abstract

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.

DOI10.1038/ncomms11514
Alternate JournalNat Commun
PubMed ID27160938
PubMed Central IDPMC4866325
Grant ListR01 AI041707 / AI / NIAID NIH HHS / United States
R01 AI097128 / AI / NIAID NIH HHS / United States
R01 AR065807 / AR / NIAMS NIH HHS / United States