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
Kataoka, Kosuke
Tokushima University
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
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
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Content Type |
Journal Article
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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.
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Journal Title |
JCI Insight
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ISSN | 23793708
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Publisher | American Society for Clinical Investigation
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Volume | 9
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Issue | 21
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Start Page | e167373
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Published Date | 2024-10-01
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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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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
Publisher
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departments |
Oral Sciences
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