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Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic T H 1 cell responses in Crohn's disease.

Gabriela Rios MartiniEkaterina TikhonovaElisa RosatiMeghan Bialt DeCelieLaura Katharina SieversFlorian TranMatthias LessingArne BergfeldSophia HinzSusanna NikolausJulia KümpersAnna MatysiakPhilipp HofmannCarina SaggauStephan SchneidersAnn-Kristin KampsGunnar JacobsWolfgang LiebJochen MaulBritta SiegmundBarbara SeegersHolger HinrichsenHans-Heinrich ObergDaniela WeschStefan BereswillMarkus M HeimesaatJan RuppOlaf KniemeyerAxel A BrakhageSascha BrunkeBernhard HubeKonrad AdenAndre FrankeIliyan D IlievAlexander ScheffoldStefan SchreiberPetra Bacher
Published in: Nature medicine (2023)
Aberrant CD4 + 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 + T cell reactions in patients with Crohn's disease (CD). Yeast-responsive CD4 + T cells in CD display a cytotoxic T helper cell (T H 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 + 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 + T cell responses in patients with CD.
Keyphrases
  • single cell
  • saccharomyces cerevisiae
  • cell therapy
  • oxidative stress
  • dendritic cells
  • stem cells
  • transcription factor
  • immune response
  • risk assessment
  • climate change
  • drug induced
  • emergency medicine