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ID 119628
Author
Kusumoto, Yutaka Osaka Ohtani University
Ueda, Mizuki Osaka Ohtani University
Hashimoto, Mayuko Osaka Ohtani University
Takeuchi, Haruka Osaka Ohtani University
Okada, Naoko Osaka Ohtani University
Yamamoto, Junya Osaka Ohtani University
Nishii, Akiko Osaka Ohtani University
Fujino, Atsuki Osaka Ohtani University
Kurahashi, Akiho Osaka Ohtani University
Satoh, Momoka Osaka Ohtani University
Iwasa, Yuki Osaka Ohtani University
Okamura, Koki Osaka Ohtani University
Obazaki, Karin Osaka Ohtani University
Kumagai, Ryoto Osaka Ohtani University
Sakamoto, Naruya Osaka Ohtani University
Tanaka, Yuto Osaka Ohtani University
Kamiya, Yukika Osaka Ohtani University
Hoshida, Tetsushi RIKEN
Kaisho, Tsuneyasu Wakayama Medical University
Hemmi, Hiroaki Wakayama Medical University|Okayama, University of Science
Katakai, Tomoya Niigata University
Honda, Tetsuya Kyoto University|Hamamatsu University School of Medicine
Kikuta, Junichi Osaka University
Ikebuchi, Ryoyo Osaka Ohtani University|Japan Society for the Promotion of Science
Moriya, Taiki Osaka Ohtani University
Adachi, Takahiro Tokyo Medical and Dental University
Watanabe, Takeshi Kyoto Universtity
Ishii, Masaru Osaka University
Miyawaki, Atsushi RIKEN
Kabashima, Kenji Kyoto University
Chtanova, Tatyana University of New South Wales Sydney|Garvan Institute of Medical Research
Tomura, Michio Osaka Ohtani University
Content Type
Journal Article
Description
The oral mucosa is the first line of defense against pathogenic bacteria and plays a vital role in maintaining tolerance to food antigens and commensal bacteria. We used CD11c reporter mice to visualize dendritic cells (DCs), a key immune cell population, in the oral cavity. We identified differences in DC density in each oral tissue region. Sublingual immune cell clusters (SLICs) extended from the lamina propria to the epithelium, where DCs and T cells resided in close contact with each other and innate lymphoid cells (ILCs). Targeted in situ photolabeling revealed that the SLICs comprised mostly of CD11c+CD11b+ DCs and were enriched for cDC1s and Langerhans cells. Although the frequency of T cell subsets was similar within and outside the SLICs, tissue resident memory T cells were significantly enriched within the clusters and cluster size increased in response to inflammation. Collectively, we found that SLICs form a unique microenvironment that facilitates T cell-DC interactions in the steady state and during inflammation. Since the oral mucosa is an important target for needle-free vaccination and sublingual immunotherapy to induce tolerogenic responses, the novel insight into the localized immunoregulation provided in this study may accelerate the development of these approaches.
Journal Title
JCI Insight
ISSN
23793708
Publisher
American Society for Clinical Investigation
Volume
9
Issue
21
Start Page
e167373
Published Date
2024-10-01
Rights
This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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DOI (Published Version)
URL ( Publisher's Version )
FullText File
language
eng
TextVersion
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departments
Oral Sciences