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Notch2-expressing CD4+ T cells attain immunoregulatory functions during autoimmune inflammation

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  • Additional Information
    • Contributors:
      Seo, Hyungseok; Koh, Seong-Joon; Park, Sung-Gyoo
    • Publication Information:
      Nature Publishing Group
    • Publication Date:
      2025
    • Collection:
      Seoul National University: S-Space
    • Abstract:
      Autoantigen-specific CD4+ T cells are central to the development of autoimmune diseases, while the expansion of regulatory T (Treg) cells expressing Forkhead box protein 3 (Foxp3) is essential for mitigating these conditions. In this study, we identified CD4+Notch2+Foxp3lo T cells in the spinal cords of mice with experimental autoimmune encephalomyelitis (EAE), dextran sodium sulfate-induced colitis model mice, and patients with ulcerative colitis as immune regulatory cells. These cells exhibited a nonproliferative, dysfunctional phenotype and demonstrated immune regulatory functions, including suppressive activity against activated CD4+ T cells and marked Treg cell expansion activity. Our data revealed that Notch2 deletion in Foxp3-expressing cells diminishes the ability of this population to reverse the clinical symptoms of EAE. Collectively, these findings suggest that Notch2 expression in dysfunctional CD4+ T cells plays a crucial role in immune regulation. ; Y ; 1
    • Relation:
      https://hdl.handle.net/10371/228033; 001534293200001; 243203
    • Accession Number:
      10.1038/s41423-025-01318-2
    • Online Access:
      https://hdl.handle.net/10371/228033
      https://doi.org/10.1038/s41423-025-01318-2
    • Accession Number:
      edsbas.C24D83AD