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Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production

Dietary antigens affect the adaptive immunity of the host by inducing regulatory T cells and IgE-producing B cells. However, their roles in innate immune compartments such as innate lymphoid cells (ILCs) and intestinal epithelial cells (IECs) are unclear. Here, using antigen-free (AF) mice, which ar...

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Autores principales: Lee, Minji, Ko, Hyun-Ja, Hong, Sung-Wook, Park, Jungeun, Ham, Seokjin, Kim, Mingyu, Kwon, Dong-il, Lee, Myeong-seok, Roh, Tae-Young, Soon Kim, Kwang, Lee, You Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076687/
https://www.ncbi.nlm.nih.gov/pubmed/35523930
http://dx.doi.org/10.1038/s41598-022-11466-4
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author Lee, Minji
Ko, Hyun-Ja
Hong, Sung-Wook
Park, Jungeun
Ham, Seokjin
Kim, Mingyu
Kwon, Dong-il
Lee, Myeong-seok
Roh, Tae-Young
Soon Kim, Kwang
Lee, You Jeong
author_facet Lee, Minji
Ko, Hyun-Ja
Hong, Sung-Wook
Park, Jungeun
Ham, Seokjin
Kim, Mingyu
Kwon, Dong-il
Lee, Myeong-seok
Roh, Tae-Young
Soon Kim, Kwang
Lee, You Jeong
author_sort Lee, Minji
collection PubMed
description Dietary antigens affect the adaptive immunity of the host by inducing regulatory T cells and IgE-producing B cells. However, their roles in innate immune compartments such as innate lymphoid cells (ILCs) and intestinal epithelial cells (IECs) are unclear. Here, using antigen-free (AF) mice, which are germ-free (GF) mice fed with amino-acid-based diet, we found dietary proteins suppress the development of GATA-3-expressing ILC2s independent of the adaptive immune cells. These cells produce more type 2 cytokines and upregulated proliferation and activation markers such as Ki-67, CD69, and CD25. With this, AF mice had increased expressions of tuft cell-specific transcripts such as Il25, Il33, Dclk1, Trpm5, and Pou2f3 in IECs. Accordingly, expanded ILC2s upregulated IL-17RB, a receptor of IL-25, and their proliferation was blocked by IL-25 neutralizing or IL-17RB blocking antibodies. These results suggest a new dialogue between dietary antigens, IECs, and ILCs in which dietary antigens suppress ILC2 activation and proliferation by restraining homeostatic IL-25 production, potentially limiting type 2 immunity by food antigens.
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spelling pubmed-90766872022-05-08 Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production Lee, Minji Ko, Hyun-Ja Hong, Sung-Wook Park, Jungeun Ham, Seokjin Kim, Mingyu Kwon, Dong-il Lee, Myeong-seok Roh, Tae-Young Soon Kim, Kwang Lee, You Jeong Sci Rep Article Dietary antigens affect the adaptive immunity of the host by inducing regulatory T cells and IgE-producing B cells. However, their roles in innate immune compartments such as innate lymphoid cells (ILCs) and intestinal epithelial cells (IECs) are unclear. Here, using antigen-free (AF) mice, which are germ-free (GF) mice fed with amino-acid-based diet, we found dietary proteins suppress the development of GATA-3-expressing ILC2s independent of the adaptive immune cells. These cells produce more type 2 cytokines and upregulated proliferation and activation markers such as Ki-67, CD69, and CD25. With this, AF mice had increased expressions of tuft cell-specific transcripts such as Il25, Il33, Dclk1, Trpm5, and Pou2f3 in IECs. Accordingly, expanded ILC2s upregulated IL-17RB, a receptor of IL-25, and their proliferation was blocked by IL-25 neutralizing or IL-17RB blocking antibodies. These results suggest a new dialogue between dietary antigens, IECs, and ILCs in which dietary antigens suppress ILC2 activation and proliferation by restraining homeostatic IL-25 production, potentially limiting type 2 immunity by food antigens. Nature Publishing Group UK 2022-05-06 /pmc/articles/PMC9076687/ /pubmed/35523930 http://dx.doi.org/10.1038/s41598-022-11466-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lee, Minji
Ko, Hyun-Ja
Hong, Sung-Wook
Park, Jungeun
Ham, Seokjin
Kim, Mingyu
Kwon, Dong-il
Lee, Myeong-seok
Roh, Tae-Young
Soon Kim, Kwang
Lee, You Jeong
Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title_full Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title_fullStr Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title_full_unstemmed Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title_short Dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic IL-25 production
title_sort dietary antigens suppress the proliferation of type 2 innate lymphoid cells by restraining homeostatic il-25 production
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076687/
https://www.ncbi.nlm.nih.gov/pubmed/35523930
http://dx.doi.org/10.1038/s41598-022-11466-4
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