Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic T<sub>H</sub>1 cell responses in Crohn's disease.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37749331.
- Also identified by DOI 10.1038/s41591-023-02556-5 and PMC identifier 10579100.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Aberrant CD4<sup>+</sup> T cell reactivity against intestinal microorganisms is considered to drive mucosal inflammation in inflammatory bowel diseases. The disease-relevant microbial species and the corresponding microorganism-specific, pathogenic T cell phenotypes remain largely unknown. In the present study, we identified common gut commensal and food-derived yeasts, as direct activators of altered CD4<sup>+</sup> T cell reactions in patients with Crohn's disease (CD). Yeast-responsive CD4<sup>+</sup> T cells in CD display a cytotoxic T helper cell (T<sub>H</sub>1 cell) phenotype and show selective expansion of T cell clones that are highly cross-reactive to several commensal, as well as food-derived, fungal species. This indicates cross-reactive T cell selection by repeated encounter with conserved fungal antigens in the context of chronic intestinal disease. Our results highlighted a role of yeasts as drivers of aberrant CD4<sup>+</sup> T cell reactivity in patients with CD and suggest that both gut-resident fungal commensals and daily dietary intake of yeasts might contribute to chronic activation of inflammatory CD4<sup>+</sup> T cell responses in patients with CD.
Medical subject headings
- Crohn Disease
- Inflammatory Bowel Diseases