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The microbiota regulates type 2 immunity through RORγt + T cells
Abstract
Gut microbes make T cells keep the peace: Our guts harbor trillions of microbial inhabitants, some of which regulate the types of immune cells that are present in the gut. For instance, Clostridium species of bacteria induce a type of T cell that promotes tolerance between the host and its microbial contents. Ohnmacht et al. and Sefik et al. characterized a population of gut regulatory T cells in mice, which required gut microbiota to survive. Multiple bacterial species of the microbiota could induce transcription factor–expressing regulatory T cells that helped maintain immune homeostasis. Mice engineered to lack these transcription factors exhibited enhanced susceptibility to colonic inflammation and had elevated amounts of proinflammatory molecules associated with allergies (see the Perspective by Hegazy and Powrie). Science , this issue pp. 989 and 993
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“Yet, Helios, Nrp-1 or ROR-γt are widely accepted for the discrimination of tTreg and pTreg cells under homeostatic conditions [364-366, 437-440].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [438]
In the citing paper
“In addition, the gut microbiome regulates the activity of retinoic acid receptor-related orphan receptor gamma-positive (RORγ+) Treg cells, dysregulation of which can lead to diseases such as colitis, food allergy, and colon cancer.622,701–704”
From Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases (2024) · cites this paper as [703]
In the citing paper
“Significantly reduced RORγt+ Tregs in GF or antibiotic-treated mice promote Th2 type-associated immune responses and inflammation upon helminth infection.134”
From Interaction between microbiota and immunity in health and disease (2020) · cites this paper as [134]
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The TNFRSF members CD27 and OX40 coordinately limit T H 17 differentiation in regulatory T cells
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Can microorganisms assist the survival and parasitism of plant-parasitic nematodes?
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IL-21 promotes allergic airway inflammation by driving apoptosis of FoxP3+ regulatory T cells
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Mucin-Type O-Glycans: Barrier, Microbiota, and Immune Anchors in Inflammatory Bowel Disease
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Spatiotemporal regulation of peripheral T cell tolerance
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Role of the intestinal mucosa in acute gastrointestinal GVHD
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CD49b defines functionally mature Treg cells that survey skin and vascular tissues
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“NLT-localized Treg cells are transcriptionally distinct from their lymphoid tissue counterparts and may exhibit distinct functional modalities (Feuerer et al., 2009; Cipolletta et al., 2012; Schiering et al., 2014; Ohnmacht et al., 2015; Sefik et al., 2015).”
BackgroundActivation pathways that drive CD4 + T cells to break tolerance in autoimmune diseases*
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Synchronization of mothers and offspring promotes tolerance and limits allergy
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Enhancing Regulatory T Cells to Treat Inflammatory and Autoimmune Diseases
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Metadata
- Authors
- Ohnmacht, C., Park, J.-H., Cording, S., Wing, J. B., Atarashi, K., Obata, Y., Gaboriau-Routhiau, V., Marques, R., Dulauroy, S., Fedoseeva, M., Busslinger, M., Cerf-Bensussan, N., Boneca, I. G., Voehringer, D., Hase, K., Honda, K., Sakaguchi, S., & Eberl, G.
- Affiliations
- Institut Pasteur (FR)
- Immunology Frontier Research Center, The University of Osaka (JP)
- Japan Science and Technology Agency (JP)
- Institute of Medical Science, The University of Tokyo (JP)
- INSERM, U1163, Laboratory of Intestinal Immunity, Paris, France.
- Helmholtz Munich (DE)
- Research Institute of Molecular Pathology (AT)
- Inserm (FR)
- Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
- Kyoto University (JP)
- Corresponding author
- Ohnmacht, Caspar
- Park, Joo-Hong
- Eberl, Gérard
- ORCID
- Venue
- Science
- Published
- 2015-08-28
- Volume
- 349
- Issue
- 6251
- Pages
- 989-993
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2126657409
- Cited by
- 863
- References
- 53
- Citations by year
- 2026: 55 · 2025: 84 · 2024: 59 · 2023: 86 · 2022: 88 · 2021: 96 · 2020: 87 · 2019: 87 · 2018: 78 · 2017: 68 · 2016: 65 · 2015: 10
- FWCI
- 36.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Site cant be reached (submittedVersion)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion)
- Funders
- Boehringer Ingelheim
- European Molecular Biology Organization
- European Commission (MEXT-CT-2006-042374)
- Agence Nationale de la Recherche (ANR 11 BSV3 020 01)
- Japan Society for the Promotion of Science (15K19129)
- Institut Pasteur
- Fondation de la Recherche Medicale (DEq. 2010318246)
- Fondation Simone e Cino Del Duca from the Institut de France
- Integrative Biology of Emerging Infectious Diseases (ANR-10-LABX-62-IBEID)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- gut microbiota, Th2 immune response, RORγt, regulatory T cells, Th17 cells, Th2 cells, helminthiasis, allergic inflammation, mucosal immunity, nuclear receptors, intestinal immune regulation
- MeSH terms
- Animals, Colitis, Ulcerative, Colon, Germ-Free Life, Homeostasis, Intestinal Mucosa, Intestine, Small, Intestines, Nematospiroides dubius, Specific Pathogen-Free Organisms, Vitamin A, T-Lymphocyte Subsets, Strongylida Infections, Th2 Cells, Models, Immunological, Immunity, Mucosal, T-Lymphocytes, Regulatory, Mice, Nuclear Receptor Subfamily 1, Group F, Member 3, Th17 Cells, Microbiota
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