Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Aug:95:102570.
doi: 10.1016/j.coi.2025.102570. Epub 2025 May 26.

Thetis cells: regulators of intestinal immune tolerance

Affiliations
Review

Thetis cells: regulators of intestinal immune tolerance

Vanja Cabric et al. Curr Opin Immunol. 2025 Aug.

Abstract

Our body's mucosal surfaces interface with the external environment and are potential sites of entry for pathogens as well as noxious substances. Yet, these barrier sites are also colonized with symbiotic microbes and are in contact with harmless environmental antigens. Different barrier epithelia harbor distinct microbial communities that shape both the epithelial layer and local immune cells that maintain tissue homeostasis and tolerance to symbiotic microbes. This seemingly paradoxical peaceful co-existence of immune cells and microbes has fascinated immunologists for decades: how does the immune system balance inflammatory and tolerogenic responses? The mechanisms underlying peripheral immune tolerance to harmless foreign antigens have been most widely studied within the intestine, where the immune system must establish and maintain tolerance to harmless food and commensal antigens. Dysregulated immune responses to these antigens are linked to several human diseases, including inflammatory bowel disease, celiac disease, and food allergy. Understanding the cellular and molecular cues that promote intestinal immune tolerance is key to the development of effective therapeutic strategies for these pathologies. Here, we review recent insights into mechanisms of intestinal tolerance with a focus on recently identified RORγt+ antigen-presenting cells.

PubMed Disclaimer

Conflict of interest statement

Declaration of Competing Interest The authors declare no competing interests.

Similar articles

References

    1. Gu Y. et al. Immune microniches shape intestinal Treg function. Nature (2024) doi: 10.1038/s41586-024-07251-0. - DOI - PMC - PubMed
    1. Yang BH et al. Foxp3+ T cells expressing RORγt represent a stable regulatory T-cell effector lineage with enhanced suppressive capacity during intestinal inflammation. Mucosal Immunol 9, (2016). - PubMed
    1. Dikiy S. et al. Terminal differentiation and persistence of effector regulatory T cells essential for preventing intestinal inflammation. Nat Immunol 26, 444–458 (2025). - PMC - PubMed
    1. Mucida D. et al. Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid. Science (1979) 317, (2007). - PubMed
    1. Coombes JL et al. A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-β -and retinoic acid-dependent mechanism. Journal of Experimental Medicine 204, (2007). - PMC - PubMed

LinkOut - more resources