• Alexander N Wein, Sean R McMaster, Shiki Takamura, Paul R Dunbar, Emily K Cartwright, Sarah L Hayward, Daniel T McManus, Takeshi Shimaoka, Satoshi Ueha, Tatsuya Tsukui, Tomoko Masumoto, Makoto Kurachi, Kouji Matsushima, and Jacob E Kohlmeier.
• Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA.
• J. Exp. Med. 2019 Dec 2; 216 (12): 2748-2762.

AbstractResident memory T cells (TRM cells) are an important first-line defense against respiratory pathogens, but the unique contributions of lung TRM cell populations to protective immunity and the factors that govern their localization to different compartments of the lung are not well understood. Here, we show that airway and interstitial TRM cells have distinct effector functions and that CXCR6 controls the partitioning of TRM cells within the lung by recruiting CD8 TRM cells to the airways. The absence of CXCR6 significantly decreases airway CD8 TRM cells due to altered trafficking of CXCR6-/- cells within the lung, and not decreased survival in the airways. CXCL16, the ligand for CXCR6, is localized primarily at the respiratory epithelium, and mice lacking CXCL16 also had decreased CD8 TRM cells in the airways. Finally, blocking CXCL16 inhibited the steady-state maintenance of airway TRM cells. Thus, the CXCR6/CXCL16 signaling axis controls the localization of TRM cells to different compartments of the lung and maintains airway TRM cells.© 2019 Wein et al.

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