The developmental pathway for CD103+ CD8+ tissue-resident memory T cells of skin

Laura K. MacKay, Azad Rahimpour, Joel Z. Ma, Nicholas Collins, Angus T. Stock, Ming Li Hafon, Javier Vega-Ramos, Pilar Lauzurica, Scott N. Mueller, Tijana Stefanovic, David C. Tscharke, William R. Heath, Michael Inouye, Francis R. Carbone*, Thomas Gebhardt

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    1001 Citations (Scopus)

    Abstract

    Tissue-resident memory T cells (T RM cells) provide superior protection against infection in extralymphoid tissues. Here we found that CD103+ CD8+ T RM cells developed in the skin from epithelium-infiltrating precursor cells that lacked expression of the effector-cell marker KLRG1. A combination of entry into the epithelium plus local signaling by interleukin 15 (IL-15) and transforming growth factor-β (TGF-β) was required for the formation of these long-lived memory cells. Notably, differentiation into T RM cells resulted in the progressive acquisition of a unique transcriptional profile that differed from that of circulating memory cells and other types of T cells that permanently reside in skin epithelium. We provide a comprehensive molecular framework for the local differentiation of a distinct peripheral population of memory cells that forms a first-line immunological defense system in barrier tissues.

    Original languageEnglish
    Pages (from-to)1294-1301
    Number of pages8
    JournalNature Immunology
    Volume14
    Issue number12
    DOIs
    Publication statusPublished - Dec 2013

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