• Shiki Takamura, Shigeki Kato, Chihiro Motozono, Takeshi Shimaoka, Satoshi Ueha, Kazuhiko Matsuo, Kosuke Miyauchi, Tomoko Masumoto, Asami Katsushima, Takashi Nakayama, Michio Tomura, Kouji Matsushima, Masato Kubo, and Masaaki Miyazawa.
• Department of Immunology, Kindai University Faculty of Medicine, Osaka, Japan takamura@med.kindai.ac.jp.
• J. Exp. Med. 2019 Dec 2; 216 (12): 2736-2747.

AbstractPopulations of CD8+ lung-resident memory T (TRM) cells persist in the interstitium and epithelium (airways) following recovery from respiratory virus infections. While it is clear that CD8+ TRM cells in the airways are dynamically maintained via the continuous recruitment of new cells, there is a vigorous debate about whether tissue-circulating effector memory T (TEM) cells are the source of these newly recruited cells. Here we definitively demonstrate that CD8+ TRM cells in the lung airways are not derived from TEM cells in the circulation, but are seeded continuously by TRM cells from the lung interstitium. This process is driven by CXCR6 that is expressed uniquely on TRM cells but not TEM cells. We further demonstrate that the lung interstitium CD8+ TRM cell population is also maintained independently of TEM cells via a homeostatic proliferation mechanism. Taken together, these data show that lung memory CD8+ TRM cells in the lung interstitium and airways are compartmentally separated from TEM cells and clarify the mechanisms underlying their maintenance.© 2019 Takamura et al.

24 keywords...

hide…